1 HORIZON SCANNING:ORTHOPAEDIC
Transcription
1 HORIZON SCANNING:ORTHOPAEDIC
HORIZON SCANNING: ORTHOPAEDIC SURGERY APRIL 2012 The object of these Horizon Scanning reports is to highlight recently completed and ongoing clinical trials, research recommendations and new and emerging health technologies. After feedback from pilot Horizon Scanning exercises and following consultation with the Arthritis Research UK Orthopaedic Surgery lead, this first Horizon Scanning report only highlights ongoing clinical trials or those completed since January 2010: follow up reports will also include research recommendations from clinical guidelines. Details of all material included in this report are shown in the appendix, sorted according to anatomical region involved. Further details of each study can be obtained via the links given to the relevant webpage. CONTENTS SEARCH METHODOLOGY RESULTS ABBREVIATIONS APPENDIX: CLINICAL TRIALS A1 Head ………………………………………………………………………………………… A2 Neck & Cervical Spine ………………………………………………………………. A3 Spine (Thoracic, Lumbar & Sacral) …………………..………………………. A3a Paediatrics 17 A3b Fracture & Injury 20 A3c Other 36 A4 Thorax ……………………………………………………………………………………... A5 Shoulder (including clavicle) ……………..…………………………………….. A5a Paediatrics 88 A5b Fracture & Injury 88 A5c Rotator cuff pathologies 95 A5d Other 104 A6 Hand & Wrist …………..………………………………………………………………. A6a Paediatrics 116 A6b Fracture & Injury 117 A6c Other 124 Written by Nadia Corp for: © Arthritis Research UK 2012 1 2 3 4 5 5 7 17 85 88 116 A7 Upper limb (including elbow) …………………………………………………… A7a Paediatrics 134 A7b Fracture & Injury 135 A7c Other 139 A8 Hip ……….…………………………..……………………………………………………... A8a Paediatrics 143 A8b Fracture & Injury 144 A8c Arthroplasty 161 A8d Other 199 A9 Knee ………………………………….……………………………………………………… A9a Paediatrics 213 A9b Fracture & Injury 214 A9c Arthroscopy 214 A9d Cruciate ligament pathologies 219 A9e Meniscus/cartilage pathologies 229 A9f Arthroplasty 235 A9g Other 288 A10 Foot & Ankle ……….……………………………………………………………………. A10a Paediatrics 301 A10b Fracture & Injury 303 A10c Arthroplasty 311 A10d Other 315 A11 Lower Limb…………….……………………………………………………………...... A11a Paediatrics 324 A11b Fracture & Injury 327 A11c Other 337 A12 General ………………….………………………………………………………………... A12a Paediatrics 346 A12b Fracture & Injury 348 A12c Other 350 134 143 213 301 324 346 SEARCH METHODOLOGY Clinical Trials Databases Searched ClinicalTrials.gov, US ISRCTN Register, UK Keywords searched Keywords and phrases were used separately or in combination; truncation was used where possible/applicable. Orthop[a]edic Surgery AND bone, spine/spinal, tendon[s], foot/feet, hand[s], joint[s], ligament[s]; Transplant AND bone, cartilage, periosteum; 2 cementoplasty; vertebroplasty; kyphoplasty; tenodesis; tenotomy; tendon transfer; arthroplasty; arthroscopy; arthrodesis; Bone AND resection, lengthening, graft; amputation; disarticulation; hemipelvectomy; discectomy; osteotomy; fasciotomy; Muscle AND resection, transposition; Fracture AND fixation, treatment; anterior cruciate ligament reconstruction; intervertebral disc chemolysis; viscosupplementation; lizarov; spine/spinal fusion; traction; limb salvage; joint capsule release; distraction osteogenesis Date limits This report includes trials that were completed or ongoing between January 2010 and April 2012. Age limits None RESULTS A total of 1,630 completed or ongoing clinical trials were identified with orthopaedics: these are tabulated in the appendix divided into anatomically distinct sections: A1: Head (n = 9); A2: Neck & Cervical spine (n = 54); A3: Spine (Thoracic, Lumbar & Sacral) (n = 416); A4: Thorax (n = 15); A5: Shoulder (including clavicle) (n = 162); A6: Hand & Wrist (n = 115); A7: Upper limb (including elbow) (n = 52); A8: Hip (n = 436); A9: Knee (n = 524); A10: Foot & Ankle (n = 140); A11: Lower limb (n = 122); A12: General (n = 163). For clarity some sections have been further divided into sub-sections including paediatrics (studies solely of individuals ≤18 years old), fracture and injury, arthroplasty, specific pathologies or groups of pathologies, and other. These are further arranged according to type of intervention: behavioural; device; dietary supplements; drug including biologics; procedure; other and 3 miscellaneous observational studies. (Trials where the end date was not specified are included based update the last update status e.g. recruitment complete etc, and follow-up time points if applicable.) Unless otherwise stated in the table trials involve participants of both genders. Each clinical study has a weblink which can be followed for further details. Where there was uncertainty regarding whether a study should be included or not (usually due to its focus), the decision aired on the side of caution and the trial was included in the feedback. ABBREVIATIONS Adult Child Comp CT CT ID F-only Grp Invite M-only n N/K NR RCT Rec Recruit Senior Susp Term Wdrwn Adult (18-65 years) Child (birth-17 years) Completed Controlled trial Clinical Trials Identifier Females only Group Enrolling by invitation Males only Enrollement Not known NR Randomized controlled trial. Recruiting Recruitment Senior (66+ years) Suspended Terminated Withdrawn 4 FULL TEXT APPENDIX SECTION B: CLINICAL TRIALS Clinical trials identity number (CT ID): Prefix of ACTRN denotes Australian New Zealand Clinical Trials Registry; ChiCTR - Chinese Clinical Trial Register; CTRI Clinical Trials Registry, India; DRK – German clinical Trials Register; NCT - National Clinical Trials Identifier; IRCT - Iranian Registry of Clinical Trials; ISRCTN International Standard Randomized Controlled Trial Number; JapicCTI - Japan Pharmaceutical Information Center Clinical Trials; JMA - Japan Medical Association Center for Clinical Trials Register; KCT - Clinical Research Information Service (CRiS), Republic of Korea; NTR – Nederland Trial Register; PACTR - Pan African Clinical Trial Registry; RPCEC - Cuban Public Registry of Clinical Trials; SLCTR - Sri Lanka Clinical Trials Registry; UKCRN – UK Clinical Research Network; UMIN – University Hospital Medical Information Network. Note: Where no end date was given the following were used: completion date for primary outcome measure – italics; last update – preceeded with a ?; start date + final timepoint of outcomes – preceeded with a >. A1. HEAD Title Phases: trial design (control) CT ID Behavioural Biofeedback-Based Cognitive Behavioral Treatment for Temporomandibular Disorders Phase II/III: RCT, safety/efficacy study NCT00769561 Device Conservative Treatment of Patients With Temporomandibular Disorders RCT, efficacy study NCT01021306 Interventions Conditions Behavioral: Temporomandibular Biofeedback-Based Disorders Cognitive Behavioral Treatment; Device: Interocclusal splint therapy Recruit n Rec 100 Adt Jun-08 Jul-10 Philipps http://ClinicalTrials.gov/show/NCT00769561 Sen University Marburg Medical Center; PsychotherapieAmbulanz Marburg e.V. 80 Adt Jan-10 Apr-12 Palmer College http://ClinicalTrials.gov/show/NCT01021306 Sen of Chiropractic; National Center for Complementary and Alternative Medicine (NCCAM); University of Iowa; Schaeffer Chiropractic Device: Chiropractic Temporomandibular Active, w/Activator & Self Disorders NR Care; Device: Dental Care & Self Care; Other: Sham AMCT; Other: Self-Care Only Group 5 Age Start (Grp) Date End Sponsors Date URL Drugs including biologics The Use of PET/CT to Evaluate Synovitis in the Temporomandibular Joint (TMJ) Phase II: Non-randomized, parallel assignment NCT01471418 Drug: PET/CT with 18-FDG Temporomandibular Joint; Conservative Treatment Therapy Rec Procedure The New Serial Treatment of Temporomandibular Disorders RCT NCT00932594 Procedure: Adjust Temporomandibular Rec the TMJ Pressure to Disorder Normal Value; Other: Do not adjust the pressure of TMJ Evaluation of Navigation Assisted Procedure: Zygomatic Fractures Rec Reconstruction of Posttraumatic Navigation Surgery; Zygomatic Deformity Procedure: Phase III: RCT, efficacy study Traditional Surgery NCT01487018 Hyperbaric Oxygen Treatment of Procedure: Osteoradionecrosis Rec Mandibular Osteoradionecrosis. A Hyperbaric oxygen Randomized Clinical Study Phase II: RCT, efficacy study NCT00760682 A Comparison of Arthrocentesis, Procedure: Temporomandibular Active, Arthroscopy and Arthroplasty in arthrocentesis; Joint Dysfunction NR the Treatment of Procedure: Temporomandibular Joint arthroscopy; Dysfunction Procedure: Non-randomised, parallel arthroplasty assignment, efficacy study NCT00636727 Miscellaneous observational studies Craniofacial Surgery Perioperative Registry Prospective study NCT00658242 Craniotomy Rec 20 Adt Dec-11 Oct-12 University of Sen Pennsylvania http://ClinicalTrials.gov/show/NCT01471418 4 Child Jan-06 Dec-16 Sun Yat-sen Adt University http://ClinicalTrials.gov/show/NCT00932594 78 Child Dec-11 Jun-15 Peking Adt University http://ClinicalTrials.gov/show/NCT01487018 114 Adt Jun-08 Apr-11 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT00760682 100 Adt Jan-07 Feb-10 Emory University http://ClinicalTrials.gov/show/NCT00636727 Sen 600 Child Mar-08 Jun-13 Children's http://ClinicalTrials.gov/show/NCT00658242 Adt Hospital of Philadelphia; Children's Anesthesiology Associates, Ltd. 6 An Evaluation of Psychological Parameters That May Influence the Outcome Following Arthroscopy and Arthroplasty for Temporomandibular Joint Surgery Prospective, cohort study NCT01396694 Psychological Predictors Rec 105 Recruit n Rec 250 Adt Jun-09 Dec-11 Emory University http://ClinicalTrials.gov/show/NCT01396694 Sen A2. NECK AND CERVICAL SPINE Title Phases: trial design (control) CT ID Behavioural Collar Immobilization Following a Posterior Cervical Laminectomy and Fusion RCT, efficacy study NCT01383876 Device GRANVIA®-C Cervical Disc Prosthesis Multicenter Pilot Study Prospective, cohort study NCT01518582 NuNEC™ disc prosthesis versus Prestige® artificial cervical disc replacement: a pilot study RCT ISRCTN63878911 Comparison of DISCOVER™ Artificial Cervical Disc and ACDF for Treatment of Cervical DDD (IDE Study) RCT, safety/efficacy study NCT00432159 Interventions Conditions Behavioral: Collar; Cervical Spondylosis Behavioral: No Collar With Symptomatic Neurological Compression Age Start (Grp) Date End Sponsors Date URL Adt Jun-11 Jun-14 Brigham and http://ClinicalTrials.gov/show/NCT01383876 Sen Women's Hospital; Massachusetts General Hospital Device: Cervical Cervicobrachial arthroplasty surgery Neuralgia; Cervical with Granvia-C Discopathy Not yet 100 Rec NuNEC™ cervical disc replacement; Prestige® cervical disc replacement Active 60 Child May-10 May-16 North Tees and http://www.controlledAdt Hartlepool NHS trials.com/ISRCTN63878911 Sen Foundation Trust (UK) Active, NR 550 Adt Jul-06 Dec-15 DePuy Spine Sen Cervical degenerative disc disease Device: Arthroplasty Cervical (DISCOVER™ Degenerative Disc Artificial Cervical Disease Disc); Device: ACDF (allograft with SLIM LOC® Anterior Cervical Plate System) 7 Adt Feb-12 Mar-17 Medicrea International http://ClinicalTrials.gov/show/NCT01518582 http://ClinicalTrials.gov/show/NCT00432159 Study to Investigate the Performance of Cervical Arthroplasty for the Treatment of Cervical Degenerative Disc Disease Phase IV: Prospective, cohort study NCT00700739 Interbody Fusion Devices in the Treatment of Cervicobrachial Syndrome RCT, safety/efficacy study NCT01511445 Device: Arthroplasty Cervical (DISCOVER™) Degenerative Disc Disease Term Device: Anterior Radiating Pain; Rec cervical discectomy Myelopathy; and fusion (ACDF) Cervicobrachial with PEEK Cage; Syndrome Device: Anterior cervical discectomy and fusion (ACDF) with a Valeo CSC Cage Study of Safety & Effectiveness of Device: PRESTIGE® Cervical Active, PRESTIGE® LP Cervical Disc vs. LP Cervical Disc; Degenerative Disc NR Anterior Cervical Fusion in Device: ATLANTIS Disease Cervical DDD Anterior Cervical Phase III: Single group Plate assignment, safety/efficacy study NCT00667459 Pivotal IDE Study of the Device: ATLANTIS™ Radiculopathy; Active, BRYAN(R) Cervical Disc Cervical Plate Myelopathy; Cervical NR Prosthesis in the Treatment of System and allograft; Degenerative Disc DDD Versus ACDF Device: BRYAN Disease RCT, safety/efficacy study Cervical Disc NCT00437190 Prosthesis A Clinical Trial Evaluating a Total Device: CerPass® Cervical Disc Invite Disc Replacement in Patients With Total Disc Disease Cervical Disc Disease Replacement Prospective, cohort study NCT01433367 An Assessment of P-15 Bone Device: P-15 Cervical Rec Putty in Anterior Cervical Fusion Synthetic Degenerative Disc With Instrumentation osteoconductive Disease (DDD) Phase III: RCT, safety/efficacy bone substitute; study Other: Autologous NCT00310440 bone 43 Adt May-08 May-15 DePuy International http://ClinicalTrials.gov/show/NCT00700739 100 Adt Dec-11 Dec-14 Amedica Sen Corporation http://ClinicalTrials.gov/show/NCT01511445 280 Adt Jan-05 Nov-14 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00667459 Sen and Biologics 494 Adt Jun-03 Oct-14 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00437190 Sen and Biologics 30 Adt May-10 Dec-13 NuVasive 180 Adt Jan-06 Aug-13 AO Clinical http://ClinicalTrials.gov/show/NCT00310440 Sen Investigation and Documentation; CeraPedics, Inc 8 http://ClinicalTrials.gov/show/NCT01433367 PRESTIGE® Cervical Disc Study Phase IV: RCT, safety/efficacy study NCT00642876 Device: Allograft Fusion and ATLANTIS™ Cervical Plate System; Device: PRESTIGE® Cervical Disc Study of the Safety and Device: PRESTIGE Effectiveness of the Artificial LP device at two Cervical Disc - Low Profile Device adjacent levels; at Two Adjacent Levels Device: Bi-level Phase III: RCT, safety/efficacy fusion with study ATLANTIS Cervical NCT00637156 Plate System Advent™ Cervical Disc Versus Device: Cervical Anterior Cervical Discectomy and Artificial Disc Fusion(ACDF) for Treatment of (Advent™ Cervical One Level Degenerative Disc Disc); Device: ACDF Disease (IDE Study) (Hallmark™ Anterior RCT, safety/efficacy study Cervical Plate NCT00637312 System with corticocancellous allograft bone) Clinical Outcomes Study Device: ACDF Evaluating the Zero-P PEEK Single group assignment NCT00945243 Porous Coated Motion (PCM) Device: Anterior Artificial Disc Cervical Discectomy Phase III: RCT, safety/efficacy and Fusion; Device: study Porous Coated NCT00578812 Motion Artificial Disc Arthroplasty Versus Fusion in Device: cervical disc Anterior Cervical Surgery: prosthesis with a Prospective Study of the Impact on mobile insert named the Adjacent Level Mobi-C; Procedure: Phase IV: RCT, efficacy study arthrodesis - cervical NCT00554528 disk surgery Degenerative Cervical Disc Disease Active, NR 541 Adt Oct-02 Jun-13 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00642876 Sen and Biologics Cervical Degenerative Disc Disease; Radiculopathy; Myelopathy Active, NR 397 Adt Jun-06 Mar-13 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00637156 Sen and Biologics Cervical Degenerative Disc Disease Term 450 Adt Mar-08 Jul-12 Orthofix Inc.; Sen Blackstone Medical dba Orthofix Spinal Implants http://ClinicalTrials.gov/show/NCT00637312 Cervical Disc Disease Active, NR 14 Adt Jul-09 Jun-12 Synthes USA Sen HQ, Inc. http://ClinicalTrials.gov/show/NCT00945243 Radiculopathy; Myelopathy Active, NR 494 Adt Jan-05 Jun-12 NuVasive http://ClinicalTrials.gov/show/NCT00578812 Rec 220 Adt May-07 May-12 Centre Hospitalier Universitaire de Nice http://ClinicalTrials.gov/show/NCT00554528 Clinical Radiculopathy; Myelopathy Due to a Cervical Disk Disease 9 Evaluating The Safety and Device: NeoDisc Effectiveness of The NeoDisc™ Versus ACDF in Subjects With Single-Level Cervical Disc Disease RCT, safety/efficacy study NCT00478088 SECURE®-C Cervical Artificial Device: SECURE-C Disc Clinical Study Cervical Artificial Phase III: RCT, safety/efficacy Disc; Procedure: study Anterior Cervical NCT00882661 Discectomy and Fusion (ACDF) Comparison of Foley Balloon With Device: foley balloon or Without Traction for the Cervical only; Device: foley Ripening balloon with weight Phase III: RCT, safety study; attached NCT01063244 Study on cervical resorbable interbody cages RCT ISRCTN57772706 Cervical Disc Degenerative Disorder Active, NR 488 Adt Sep-06 Mar-12 NuVasive http://ClinicalTrials.gov/show/NCT00478088 Symptomatic Cervical Disc Disease Active, NR 380 Adt http://ClinicalTrials.gov/show/NCT00882661 Cervical Ripening Solis (non-resorbable Degenerative disc PEEK) interbody disease of the cage device (no cervical spine internal fixation); Solis RS (bioresorbable PLLA) interbody cage device (no internal fixation) Pilot Study to Assess the Efficacy Device: Lubo cervical Elective Surgical and Safety of the Lubo Cervical collar Procedure Collar Phase I: Single group assignment, safety study NCT00355173 Prospective International Stand-alone Cervical multicentre Evaluation of polyetheretherketone degenerative disc Radiological and Clinical Effects of (PEEK) intervertebral disease stand-alone polyetheretherketone spacers (PEEK) intervertebral spacers for anterior cervical discectomy and fusion (ACDF) Observational study ISRCTN42774128 Rec Comp Jul-05 Mar-12 Globus Medical Inc Adt Jan-09 Jan-11 St. Luke's http://ClinicalTrials.gov/show/NCT01063244 Hospital, FPennsylvania; St only Luke's Hopsital OB/Residency program 113 Adt Aug-07 Dec-10 Stryker SA http://www.controlledSen (Switzerland) trials.com/ISRCTN57772706 70 Comp 50 Adt May-06 Nov-10 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00355173 Comp 200 Adt Sep-06 Jan-10 Deutsche Sen Arthrose Hilfe e.V. (Germany) http://www.controlledtrials.com/ISRCTN42774128 10 Drugs including biologics Efficacy of Riluzole in Surgical Treatment for Cervical Spondylotic Myelopathy (CSM-Protect) Phase III: RCT, efficacy study NCT01257828 Study Comparing Short Term Efficacy of Dysport® and Dysport RU® to Placebo, and to Assess Efficacy and Safety of Dysport RU® of Subjects With Cervical Dystonia Phase III: RCT, efficacy study NCT01261611 PureGen: A Radiographic Analysis of Rate and Quality of Fusion in Patients Undergoing Anterior Cervical Discectomy and Fusion (ACDF) Prospective, cohort study NCT01291134 Safety and Efficacy of Cethrin® in Adult Subjects With Acute Cervical Spinal Cord Injury Phase II: RCT, safety/efficacy study NCT00610337 Procedure Anterior Vs Posterior Procedures for Cervical Spondylotic Myelopathy: Prospective Randomized Clinical Trial Prospective, cohort study NCT00876603 Drug: riluzole; Drug: Cervical Spondylotic Placebo medication Myelopathy Rec 270 Adt Dec-11 Jul-13 SpineNet Sen http://ClinicalTrials.gov/show/NCT01257828 Drug: Botulinum type Cervical Dystonia A toxin (Dysport RU®); Drug: Botulinum type A toxin (Dysport®); Drug: Placebo Rec 350 Adt Apr-11 Mar-13 Ipsen Sen http://ClinicalTrials.gov/show/NCT01261611 Biological: PureGen Cervical Osteoprogenitor Cell Degenerative Disc Allograft Disease Rec 50 Adt Feb-11 Oct-11 Alphatec Spine, Sen Inc. http://ClinicalTrials.gov/show/NCT01291134 Drug: Cethrin® (BA- Acute Cervical 210); Procedure: Spinal Cord Injury placebo Term 200 Adt Procedure: ACDF; Cervical Spondylotic Procedure: Cervical Myelopathy laminoplasty Rec 100 Adt May-01 Dec-20 The University of http://ClinicalTrials.gov/show/NCT00876603 Sen Hong Kong 11 Feb-10 Alseres http://ClinicalTrials.gov/show/NCT00610337 Pharmaceuticals, Inc Treatment of Cervical Radiculopathy With Arthroplasty Compared With Discectomy With Fusion and Cage (ACDF) RCT, efficacy study NCT00735176 Procedure: Cervical Radiculopathy, arthroplasty; Cervical Procedure: Anterior cervical discectomy and fusion (ACDF) Conservative or Operative Procedure: Bouquet Fractures of the Treatment of Fractures in the Neck pinning of the 5th Neck of the 5th Metacarpal Bone metacarpal bone RCT, efficacy study NCT01139528 Safety and Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical Discectomy and Fusion Phase II: RCT, safety/efficacy study NCT01106417 Safety and Preliminary Efficacy Study of NeoFuse in Subjects Undergoing Multi-Level Anterior Cervical Discectomy Phase II: RCT, safety/efficacy study NCT01097486 Improvement of Trans-operatory X-ray Visualization During Anterior Cervical Surgery Single group assignment, safety/efficacy study NCT01342575 Procedure: Anterior Cervical Cervical Discectomy Degenerative Disc and Fusion with Disease; NeoFuse; Procedure: Degenerative Anterior Cervical Spondylolisthesis; Discectomy and Spinal Stenosis Fusion with Granules Procedure: Anterior Cervical Cervical Discectomy Degenerative Disc and Fusion with Disease; NeoFuse; Procedure: Degenerative Anterior Cervical Spondylolisthesis; Discectomy and Spinal Stenosis Fusion with Allograft Procedure: IntraVisualization During operative exposure Cervical Spine maneuvers Surgery Rec 146 Rec 120 Active, NR 12 Rec 24 Adt Jun-10 Dec-12 Mesoblast, Ltd. Sen Rec 50 Adt Dec-10 Apr-12 American British http://ClinicalTrials.gov/show/NCT01342575 Sen Cowdray Medical Center 12 Adt Sep-08 Sep-18 Norwegian http://ClinicalTrials.gov/show/NCT00735176 University of Science and Technology; Rikshospitalet University Hospital; Haukeland University Hospital; Ullevaal University Hospital; University Hospital of North Norway; St. Olavs Hospital Adt May-10 Dec-13 Oslo University http://ClinicalTrials.gov/show/NCT01139528 Sen Hospital; University Hospital, Akershus; Asker & Baerum Hospital Adt Jun-10 Jun-13 Mesoblast, Ltd. http://ClinicalTrials.gov/show/NCT01106417 Sen http://ClinicalTrials.gov/show/NCT01097486 Surgical Treatment of Cervical Spondylotic Myelopathy Phase IV: Single group assignment, efficacy study NCT00565734 Comparing Surgical to Conservative Management in the Treatment of Type II Odontoid Fractures Among the Elderly Phase IV: Single group assignment, safety/efficacy study NCT00283998 Reducing Dysphagia Associated With Anterior Cervical Spine Surgery by Maintaining Low Endotracheal Tube Cuff Pressure RCT, efficacy study NCT00332683 Procedure: standard Cervical Spondylotic Active, surgical care for Myelopathy NR CSM treatment 375 Procedure: surgical Odontoid Fractures versus conservative Type II treatment 166 Rec Procedure: Deglutition Disorders Rec Maintaining low (15mmHg) ETT cuff pressure; Procedure: Maintaining a normal pressure in the ETT cuff Cervical Restorations Placed Procedure: Relative Non-carious Cervical Active, Under Two Isolation Methods isolation with cotton Lesions NR Phase II/III: RCT, efficacy study rolls; Procedure: NCT01506830 Absolute isolation with rubber dam Treatment of Type II Odontoid Procedure: surgical; Neck Injuries; Spinal Comp Fractures Among the Elderly Procedure: Injuries Phase IV: Single group conservative assignment, safety/efficacy treatment study NCT00266929 The CSM Trial: A Multicenter Procedure: Ventral Cervical Spondylotic Active, Study Comparing Ventral to Dorsal Surgical Myelopathy NR Surgery for Cervical Spondylotic Decompression with Myelopathy Instrumented Fusion; Phase III: Non-randomized, Procedure: Dorsal parallel assignment, Decompression With safety/efficacy study or Without Fusion NCT00506558 Adt Nov-07 Apr-12 AO Clinical http://ClinicalTrials.gov/show/NCT00565734 Sen Investigation and Documentation; AOSpine International Adt Jan-06 Mar-12 AO Clinical http://ClinicalTrials.gov/show/NCT00283998 Sen Investigation and Documentation; AOSpine North America 40 Adt Sep-06 Dec-11 Lawson Health Research Institute http://ClinicalTrials.gov/show/NCT00332683 30 Adt Jul-09 Jul-11 Federal Sen University of Pelotas http://ClinicalTrials.gov/show/NCT01506830 166 Adt Dec-05 Mar-11 AO Clinical http://ClinicalTrials.gov/show/NCT00266929 Sen Investigation and Documentation; AOSpine North America 100 Adt Nov-06 Feb-11 Greenwich Sen Hospital; Yale University 13 http://ClinicalTrials.gov/show/NCT00506558 A Clinical Trial Evaluating a Total Cervical spinal Disc Replacement in Patients with reconstruction Cervical Disc Disease Non-randomized (historical), efficacy study ISRCTN83445469 Safety Study of Preservon-Treated Procedure: Anterior Bone Implants for Cervical Fusion Cervical Discectomy in the Treatment of Cervical and Fusion Radiculopathy or Myelopathy RCT, safety/efficacy study NCT00344890 Laminectomy without or with Laminectomy; dorsal Fusion for cervical laminectomy and myeloradiculopathy: a randomised fusion. trial RCT ISRCTN72800446 Other Outcome of Physiotherapy After Surgery for Cervical Disc Disease: a Prospective Multi-Centre Trial RCT, efficacy study NCT01547611 Shi-style Cervical Manipulations for Cervical Radiculopathy RCT, safety/efficacy study NCT01500967 Degenerative Disc Disease Cervical Radiculopathy; Myelopathy Comp 30 Adt May-10 Dec-10 Nuvasive Inc. Sen (USA) http://www.controlledtrials.com/ISRCTN83445469 Rec 120 Adt Sep-06 Dec-10 LifeNet Health http://ClinicalTrials.gov/show/NCT00344890 60 Adt Jan-07 Jan-10 Radboud Sen University Nijmegen (The Netherlands) http://www.controlledtrials.com/ISRCTN72800446 Adt Jan-09 Dec-17 Linkoeping http://ClinicalTrials.gov/show/NCT01547611 Sen University; University Hospital, Linkoeping; Karolinska University Hospital; Ryhov County Hospital; Lund University Hospital Adt Dec-11 May-14 Shanghai http://ClinicalTrials.gov/show/NCT01500967 University of Traditional Chinese Medicine; Tianjin University of Traditional Chinese Medicine Cervical myelopathy Comp due to cervical spinal stenosis Other: Customary Radiculopathy treatment; Other: Structured behavioural medicine program Rec 200 Other: Shi-style Cervical cervical Radiculopathy manipulations; Other: Cervical Traction control Rec 648 14 Comparison of Outcomes Between Other: early physical Early Physical Therapy therapy intervention; Intervention and Usual Care Other: usual care Following Anterior Cervical Fusion Surgery RCT, efficacy study NCT01519115 The Value of Traction in the Other: Physical Treatment of Cervical therapy Radiculopathy rehabilitation; Other: Phase III: RCT Physical therapy NCT00979108 rehabilitation; Other: Physical therapy rehabilitation Effectiveness of Manual Therapy in Patients With Neck Pain. RCT, efficacy study NCT00713843 Other: Manual Therapy Utrecht; Other: Physical Therapy Effects of Gua Sha and Other: Gua Sha; Thermotherapy on Chronic Neck Device: Pain Thermotherapy RCT NCT01233180 Safety Study of Preservon-Treated Procedure: Anterior Bone Implants for Cervical Fusion Cervical Discectomy in the Treatment of Cervical and Fusion Radiculopathy or Myelopathy RCT, safety/efficacy study NCT00344890 Evaluation of the Nursing C-Spine Other: Clinical (Phase IV) decision rule Phase IV: Single group clearing the c-spine assignment NCT01353352 Cervical Spine Degenerative Disc Disease; Fusion of Spine, Cervical Region Not yet Rec 40 Radiculopathy; Neck Rec Pain; Spinal Diseases; Musculoskeletal Diseases; Neuromuscular Diseases; Intervertebral Disk Displacement Neck Pain Active, NR 192 Neck Pain Comp 50 Rec 120 Cervical Radiculopathy; Myelopathy Fracture of Cervical Spine; Fracture Dislocation of Cervical Spine 180 Adt Jan-12 Dec-12 Texas Woman's http://ClinicalTrials.gov/show/NCT01519115 Sen University; Texas Society of Allied Health Professions; Texas Spine and Joint Hospital Adt Jul-09 Jul-12 Intermountain http://ClinicalTrials.gov/show/NCT00979108 Sen Health Care, Inc.; University of Utah; Wilford Hall Medical Center; Empi, A DJO Company Adt Sep-08 Feb-12 Radboud http://ClinicalTrials.gov/show/NCT00713843 Sen University; Stichting Garantiefonds Spaarneland, The Netherlands Adt Sep-10 Feb-11 Universität http://ClinicalTrials.gov/show/NCT01233180 Sen Duisburg-Essen Adt Sep-06 Dec-10 LifeNet Health http://ClinicalTrials.gov/show/NCT00344890 Comp 3633 Child Jan-08 Aug-10 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01353352 Adt Research Sen Institute; Canadian Institutes of Health Research 15 Miscellaneous observational studies MaxAn Post Market Surveillance Validation Prospective, case-only study NCT01343693 Comparing Outcomes of Elbow Extension Tendon Transfers Retrospective, cohort study NCT01204736 Comparison of Cage Versus Plate in One Level Cervical Disc Disease Prospective, cohort study NCT01011569 PRESTIGE Observational Study Prospective study NCT00875810 Trinity Evolution in Anterior Cervical Disectomy and Fusion (ACDF) Prospective, case-only study NCT00951938 DDD; Deformity; Tumor; Fracture Rec 200 Adt Jun-11 Feb-15 Biomet, Inc. Sen Cervical Spinal Cord Injury Rec 45 Cervical Disc Disease Rec 80 Adt Aug-11 Sep-14 Department of http://ClinicalTrials.gov/show/NCT01204736 Veterans Affairs; Rehabilitation Institute of Chicago; Northwestern University; Case Western Reserve University; Loyola University Adt Apr-04 Mar-13 Seoul National http://ClinicalTrials.gov/show/NCT01011569 Sen University Hospital Active, NR 225 Adt Apr-08 Jan-13 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00875810 Sen & Biologics ECA Active, NR 200 Adt Aug-09 Apr-12 Orthofix Inc. Sen Degenerative Cervical Disc Disease Degenerative Disc Disease 16 http://ClinicalTrials.gov/show/NCT01343693 http://ClinicalTrials.gov/show/NCT00951938 A3. SPINE (Thoracic, Lumbar & Sacral) A3A: PAEDIATRICS Title Phases: trial design (control) CT ID Behavioural Study of the Effects of Hypnosis Before Undergoing Surgery, on Anxiety in Children Aged 10 to 18 Years RCT, efficacy study NCT01320956 Device Bracing in Adolescent Idiopathic Scoliosis Trial (BrAIST) Phase III: RCT NCT00448448 Dietary supplements Growth Hormone Therapy and Bone Quality in Pediatric Osteoporosis Phase III: RCT, efficacy study NCT00757393 Interventions Conditions Behavioral: Pre Osteotomy and operative nurse Spinal Column consultation and Surgery Hypnosis; Other: Pre operative nurse consultation Device: Brace; Other: Watchful waiting Adolescent Idiopathic Scoliosis Dietary Supplement: Osteoporosis Vitamin D + Calcium + Exercise program; Drug: Vitamin D + Calcium + Exercise program + Humatrope Recruit Rec n Age Start (Grp) Date End Sponsors Date 120 Child Mar-11 Sep-13 Assistance Publique Hôpitaux de Paris URL http://ClinicalTrials.gov/show/NCT01320956 Active, NR 500 Child Feb-07 Aug-12 University of http://ClinicalTrials.gov/show/NCT00448448 Iowa; National Institute of Arthritis and Musculoskeletal and Skin Diseases; Canadian Institutes of Health Research; Shriners Hospitals for Children; Children's Mercy Hospital Kansas City; University of Rochester Not yet Rec 28 17 Child Sep-08 Jan-12 The Hospital for http://ClinicalTrials.gov/show/NCT00757393 Sick Children Drugs including biologics Autologous Stem Cells for Spinal Cord Injury (SCI) in Children Phase I: Single group assignment, safety/efficacy study NCT01328860 Non-Idiopathic Scoliosis Treated With Tranexamic Acid Phase II: RCT, efficacy study NCT01089140 Biological: bone marrow progenitor cells (BMPC) autologous transplantation Spinal Cord Injury Drug: Tranexamic Non-idiopathic acid 10mg/kg/hr; Scoliosis Drug: Tranexamic acid 100 mg/kg/h infusion; Drug: Saline solution An Efficacy and Safety Trial of Drug: Zoledronic Osteoporosis Intravenous Zoledronic Acid Twice acid; Drug: Placebo Yearly in Osteoporotic Children Treated With Glucocorticoids for Chronic Inflammatory Conditions Phase III: RCT, safety/efficacy study NCT00799266 The Use of Intraoperative Drug: DepoDur™ Pain Management; Intrathecal Morphine Versus Spinal Fusion; Epidural Extended Release Scoliosis Morphine for Postoperative Pain Control in Pediatric Patients Undergoing Posterior Spinal Fusion Phase IV: RCT, safety/efficacy study NCT00880607 Rec Rec 10 Child Apr-11 Oct-14 Memorial http://ClinicalTrials.gov/show/NCT01328860 Hermann Healthcare System; Institute for Rehabilitaion and Research Foundation; The University of Texas; Anderson Cancer Center; Baylor College of Medicine; Methodist Hospital System Research Institute, Houston 120 Child Nov-09 Nov-12 The Hospital for http://ClinicalTrials.gov/show/NCT01089140 Sick Children Rec 92 Child Dec-08 Oct-12 Novartis http://ClinicalTrials.gov/show/NCT00799266 Rec 80 Child Dec-08 Dec-11 Children's Hospital Colorad; University of Colorado, Denver http://ClinicalTrials.gov/show/NCT00880607 18 Peri-operative pain management in Epidural infusion of Post-operative pain children and adolescents bupivacine, after scoliosis undergoing scoliosis surgery: pain, epinephrine and surgery nausea and psychological impact fentanyl + patient RCT, efficacy study controlled extra ISRCTN12885779 boluses; intravenous infusion of (S)ketaminehydrochlorid Alendronate in Juvenile Drug: Alendronate Juvenile Osteoporosis (Fosamax) Osteoporosis; Low NCT00920075 Bone Density; Fractures Other Prospective Study of Scoliosis in Children With Cerebral Palsy Prospective, case control study NCT00680264 Dexmedetomidine on Intraoperative Somatosensory and Motor Evoked Potential Monitoring During Neurosurgery in Pediatric Patients Single group assignment, safety study NCT01512147 Effect of High-Calcium Milk and Weight-Bearing Exercise on Bone Mineral Status of Pre-Pubertal Girls RCT NCT00979511 Comp 38 Child Apr-09 Apr-11 University http://www.controlledHospital of trials.com/ISRCTN12885779 Nothern Sweden (Sweden) Comp 11 Child Jul-09 Oct-10 Medical http://ClinicalTrials.gov/show/NCT00920075 Adt University of South Carolina; FDA Office of Orphan Products Development; Merck Cerebral Palsy; Scoliosis Rec Other: Isoflurane, Propofol, Dexmedetomidine Tethered Spinal Cord; Brain Tumor; Cranio Cervical Compression Rec Other: milk and exercise Osteoporosis Miscellaneous observational studies Shilla Growth Permitting Spinal Instrumentation System for Treatment of Scoliosis in the Immature Spine Prospective study NCT00577226 Scoliosis Active, NR Term 402 Child Jun-08 Dec-15 Harms Study Adt Group Foundation; DePuy Spine 20 Child Dec-11 Dec-12 Oregon Health and Science University http://ClinicalTrials.gov/show/NCT00680264 http://ClinicalTrials.gov/show/NCT01512147 120 Child Feb-09 Dec-10 Nutrition Center http://ClinicalTrials.gov/show/NCT00979511 of the FPhilippines; only Nestlé Foundation 50 19 Child Apr-05 Apr-15 Arkansas Children's Hospital Research Institute http://ClinicalTrials.gov/show/NCT00577226 Study of the Surgical Treatment of Early Onset Scoliosis Using a Noninvasive Growing Rod Prospective, cohort study NCT01362881 Risk Factors for Psychiatric Disorders Associated With Adolescent Idiopathic Scoliosis Prospective, cohort study NCT00958373 Scoliosis Rec 50 Child Jan-12 Jan-15 Surgi C Limited http://ClinicalTrials.gov/show/NCT01362881 Adolescent Idiopathic Scoliosis Term 0 Child Oct-06 Mar-11 University of http://ClinicalTrials.gov/show/NCT00958373 British Columbia Recruit n Age Start (Grp) Date Rec 150 Adt Apr-11 Dec-14 Department of http://ClinicalTrials.gov/show/NCT01093014 Sen Veterans Affairs; University of Iowa Rec 160 Adt Sep-09 Jan-13 University of Sen Washington Rec 72 Adt Aug-10 Dec-12 University of http://ClinicalTrials.gov/show/NCT01184365 British Columbia; Canadian Institutes of Health Research A3B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Behavioural Novel Intervention to Influence Muscle Plasticity in Veterans Single group assignment, efficacy study NCT01093014 Telephone Intervention for Pain Study (TIPS) RCT, efficacy study NCT00663663 Interventions Conditions Behavioral: Active Resisted Standing Spinal Cord Injuries Behavioral: Chronic Pain; Telephone-Delivered Multiple Sclerosis; Intervention 1; Amputation; Spinal Behavioral: Cord Injury Telephone-Delivered Intervention 2 Spinal Cord Injury Energy Behavioral: Energy Spinal Cord Injury Management Program Management Phase II/III: RCT, efficacy study Program; Behavioral: NCT01184365 Energy Management Program 20 End Sponsors Date URL http://ClinicalTrials.gov/show/NCT00663663 Addressing Vertebral Osteoporosis Behavioral: Osteoporosis Incidentally Detected to Prevent Reminders and Future Fractures opinion leader Non-randomized, parallel generated guidelines assignment, safety/efficacy +/- leaflets and study counselling; Other: NCT00388908 Usual Care Active, NR 240 Adt Nov-06 May-11 University of http://ClinicalTrials.gov/show/NCT00388908 Sen Alberta; Canadian Institutes of Health Research Spinal Cord Injuries; Stroke; Paralysis; Tetraplegia; Paraplegia Rec 25 Device: Lokomat treadmill training; Other: Aquatic exercise therapy Spinal Cord Injury Rec 36 Device: Vertebral Augmentation (STABILIT); Other: Non-operative Management Painful Osteoporotic Vertebral Compression Fractures (VCF) Rec 130 Adt May-05 Jun-15 Case Western http://ClinicalTrials.gov/show/NCT00623389 Sen Reserve University; National Institutes of Health; Department of Veterans Affairs Adt Apr-11 Dec-14 University of http://ClinicalTrials.gov/show/NCT01407354 Maryland; Shepherd Center, Virginia C. Crawford Research Institute Adt Nov-11 Nov-14 DFINE Inc. http://ClinicalTrials.gov/show/NCT01480167 Sen Device: Vertebral Augmentation (STABILIT); Other: Non-operative Management Painful Osteoporotic Vertebral Compression Fractures (VCF) Rec 130 Adt Nov-11 Nov-14 DFINE Inc. Sen Rec 10 Adt Sen Device Evaluation of an Advanced Lower Device: IST-16 (16Extremity Neuroprostheses channel implanted Single group assignment, stimulator-telemeter) safety/efficacy study NCT00623389 Comparison of Lokomat and Aquatic Exercise for Individuals With Chronic Incomplete Spinal Cord Injury Phase I: RCT, safety/efficacy study NCT01407354 The PRIORi-T Trial--Prospective Randomized Investigation of Radiofrequency Targeted Vertebral Augmentation Phase IV: RCT, efficacy study NCT01480167 The PRIORi-T Trial--Prospective Randomized Investigation of Radiofrequency Targeted Vertebral Augmentation Phase IV: RCT, efficacy study NCT01480167 A Neuroprosthesis for Seated Posture and Balance Phase I: Single group assignment, safety/efficacy study NCT01474148 Device: IRS-8 (8Spinal Cord Injury; Channel implanted Paralysis; stimulator-telemeter) Tetraplegia; Paraplegia 21 http://ClinicalTrials.gov/show/NCT01480167 Jul-11 Jan-14 Case Western http://ClinicalTrials.gov/show/NCT01474148 Reserve University; Department of Veterans Affairs Evaluation of safety and Osseofix Spinal effectiveness of the Osseofix Fracture Reduction Spinal Fracture Reduction System System in treating spinal compression fractures Prospective, cohort study ISRCTN26909676 OsseoFix™ Spinal Fracture Device: OsseoFix Reduction System in Treating Spinal Fracture Spinal Compression Fracture Reduction System Phase II/III: Non-randomized, parallel assignment, safety/efficacy study NCT00961714 Comparison of Balloon Device: balloon Kyphoplasty and Vertebroplasty in kyphoplasty; Subacute Osteoporotic Vertebral Procedure: Fractures vertebroplasty Phase IV: RCT, safety/efficacy study NCT00749086 Comparison of Balloon Device: balloon Kyphoplasty and Vertebroplasty in kyphoplasty; Subacute Osteoporotic Vertebral Procedure: Fractures vertebroplasty Phase IV: RCT, safety/efficacy study NCT00749086 Clinical Evaluation of the Device: Crosstrees Crosstrees Pod™ in the Treatment Pod system for PVA of Pathologic Fracture of the Vertebral Body (Levels T4 - L5) in Adult Patients Single group assignment, safety/efficacy study NCT00933036 Vertebral fractures Active 150 Adt Nov-11 Nov-13 Alphatec Spine Sen (UK) Vertebral Compression Fractures Rec 125 Adt Aug-09 Jul-13 Alphatec Spine, http://ClinicalTrials.gov/show/NCT00961714 Sen Inc. Osteoporotic Vertebral Fracture; Between T5 and L5; Chronic Arthritis, Longer Than Six Weeks Duration Rec 200 Adt Dec-07 Dec-12 Assistance http://ClinicalTrials.gov/show/NCT00749086 Sen Publique Hôpitaux de Paris; Ministry of Health, France Osteoporotic Vertebral Fracture; Between T5 and L5; Chronic Arthritis, Longer Than Six Weeks Duration Rec 200 Adt Dec-07 Dec-12 Assistance http://ClinicalTrials.gov/show/NCT00749086 Sen Publique Hôpitaux de Paris; Ministry of Health, France Pathologic Fracture of the Vertebra Due to Osteoporosis Rec 118 Adt Jun-09 Dec-12 Crosstrees Sen Medical Inc. 22 http://www.controlledtrials.com/ISRCTN26909676/ http://ClinicalTrials.gov/show/NCT00933036 Clinical Evaluation of the Device: Crosstrees Crosstrees Pod™ in the Treatment Pod system for PVA of Pathologic Fracture of the Vertebral Body (Levels T4 - L5) in Adult Patients Single group assignment, safety/efficacy study NCT00933036 The Kiva® System as a Vertebral Device: Vertebral Augmentation Treatment augmentation Phase III: RCT, safety/efficacy study NCT01123512 DuraGen Plus® Adhesion Barrier Device: DuraGen for Use in Spinal Surgery Plus Adhesion RCT, safety/efficacy study Barrier Matrix NCT00387829 Influence of Bone Strength Device: DensiProbe Measured by DensiProbe on Bone Hip Related Fixation Failure Single group assignment NCT00822159 Unipedicular vs. Bipedicular Device: Kyphon® Kyphoplasty for the Treatment of Balloon Kyphoplasty Osteoporotic Vertebral Fractures (Kyphon Inc; Phase IV: RCT, safety/efficacy Sunnydale, CA) study NCT01383616 Unipedicular vs. Bipedicular Device: Kyphon® Kyphoplasty for the Treatment of Balloon Kyphoplasty Osteoporotic Vertebral Fractures (Kyphon Inc; Phase IV: RCT, safety/efficacy Sunnydale, CA) study NCT01383616 Monopolar Electrosurgery Versus Device: ultrasound Ultrasound Scissors in scissors - Harmonic Thoracoscopic Ventral ACE; Device: Spondylodesis electroscalpel (Erbe Phase IV: RCT, safety/efficacy Vio 300; Aesculap study AG) NCT00941213 Pathologic Fracture of the Vertebra Due to Osteoporosis Rec 118 Adt Jun-09 Dec-12 Crosstrees Sen Medical Inc. http://ClinicalTrials.gov/show/NCT00933036 Spinal Fractures; Fractures, Compression; Back Injuries Rec 425 Adt Sen Jul-10 Aug-12 Benvenue Medical, Inc. http://ClinicalTrials.gov/show/NCT01123512 Spinal Injuries; Adhesions Term 500 Adt Oct-06 Dec-11 Integra Sen LifeSciences Corporation http://ClinicalTrials.gov/show/NCT00387829 Femoral Fractures; Hip Fractures; Osteoporosis; Bone Density Term 198 Adt Nov-08 Sep-11 AO Clinical http://ClinicalTrials.gov/show/NCT00822159 Sen Investigation and Documentation Vertebral Compression Fracture Active, NR 45 Adt Sen Jul-06 Sep-11 Hospital for http://ClinicalTrials.gov/show/NCT01383616 Special Surgery, New York Vertebral Compression Fracture Active, NR 45 Adt Sen Jul-06 Sep-11 Hospital for http://ClinicalTrials.gov/show/NCT01383616 Special Surgery, New York Rec 40 Adt Dec-09 Aug-11 University of http://ClinicalTrials.gov/show/NCT00941213 Sen Cologne; Ethicon EndoSurgery (Europe) GmbH Fractures of Vertebral Bodies 23 Cardiovascular Fitness for Robotically Assisted Treadmill Training in Persons With Chronic Incomplete Spinal Cord Injury RCT, efficacy study NCT00385918 Device: Lokomat Training; Other: Home stretching protocol Feasibility Study of Balloon Device: balloon Kyphoplasty in Traumatic Vertebral kyphoplasty Fractures Needing Surgical Fixation Phase IV: Single group assignement, safety/efficacy study NCT00749229 Treatment of Malignant Vertebral Device: balloon Fractures With Percutaneous kyphoplasty Balloon Kyphoplasty. Single group assignment, safety/efficacy study NCT00748631 Medtronic SCORE Study - Study Device: Kyphon® of Curette Use for Obtaining Curette Restoration of Vertebral Body Anatomy in Balloon Kyphoplasty Phase IV: RCT, safety/efficacy study NCT00810043 Medico-Economical Impact of the Device: Brindley Brindley Neurosurgical Technique technique (bladder in France system) Non-randomized, parallel assignment, safety/efficacy study NCT00221767 The Effect of AposTherapy on the Device: Level of Pain, Function and Quality AposTherapy of Life in Patients With Neuromuscular and Neurological Disorders NCT01266382 Paraplegia; Quadriplegia; Spinal Cord Injury; Tetraplegia Comp 40 One or Two Traumatic Vertebral Fractures; Located Between T11 and L5,; Balloon Kyphoplasty Term 17 Vertebral Fracture; Multiple Myeloma; Osteolytic Metastases Term 60 Adt Oct-07 Nov-10 Assistance Sen Publique Hôpitaux de Paris Vertebral Body Compression Fractures (VCFs) Comp 120 Adt Feb-09 Oct-10 Medtronic Spine http://ClinicalTrials.gov/show/NCT00810043 Sen LLC Spinal Cord Injuries; Active, Neurogenic Bladder NR Disorder; Paraplegia; Quadriplegia 53 Adt Jun-05 Apr-10 University Sen Hospital, Bordeaux; Ministry of Health, France Osteoarthritis; Spinal Diseases; Ligament Rupture; Lower Extremity Fracture; Neurological Disorders N/K Adt Sen Rec 24 Adt Oct-06 Jun-11 Department of http://ClinicalTrials.gov/show/NCT00385918 Sen Veterans Affairs; University of Maryland; Kernan Orthopaedics & Rehabilitation Hospital Adt Dec-07 Mar-11 Assistance http://ClinicalTrials.gov/show/NCT00749229 Sen Publique Hôpitaux de Paris; Ministry of Health, France N/K http://ClinicalTrials.gov/show/NCT00748631 http://ClinicalTrials.gov/show/NCT00221767 Jul-09 Assaf-Harofeh http://ClinicalTrials.gov/show/NCT01266382 Medical Center; Apos Medical and Sports Technology Ltd. Dietary supplements Analgesic Effects of the Gastrolith, Dietary Supplement: Osteoporosis in Osteoporotic Patients Suffering Gastrolith; Other: From Recent Skeletal Pain Placebo Caused by Vertebral Fractures Phase IV: RCT, safety/efficacy study NCT01482858 Drugs including biologics Comparison of the Effect of an Ongoing Treatment With Alendronate or a Drug Holiday on the Fracture Risk in Osteoporotic Patients With Bisphosphonate Long Term Therapy Phase III: RCT, safety/efficacy study NCT01512446 Mesenchymal Stem Cells Transplantation to Patients With Spinal Cord Injury Phase I/II: Single group assignment, safety/efficacy study NCT01446640 Safety Study of GRNOPC1 in Spinal Cord Injury Phase I: Single group assignment, safety study NCT01217008 Denosumab Fracture Intervention Randomized Placebo Controlled Trial in Japanese Patients With Osteoporosis Phase III: RCT, safety/efficacy study NCT00680953 Not yet Rec 80 Drug: Alendronate; Drug: Placebo Osteoporosis Biological: bone marrow derived mesenchymal stem cells Spinal Cord Injury Rec 20 Biological: GRNOPC1 Spinal Cord Injury Active, NR 10 Drug: Denosumab; Osteoporosis Drug: Placebo; Drug: Alendronate sodium hydrate Adt Dec-11 Aug-12 Amorphical Ltd. http://ClinicalTrials.gov/show/NCT01482858 Sen Not yet 7000 Adt Jan-12 Mar-15 Evangelisches http://ClinicalTrials.gov/show/NCT01512446 Rec Sen Krankenhaus Lutherhaus gGmbH; German Federal Ministry of Education and Research Child Oct-11 Jun-14 Guangzhou http://ClinicalTrials.gov/show/NCT01446640 Adt General Hospital of Guangzhou Military Command Adt Oct-10 Oct-12 Geron Corporation Active, 1100 Adt May-08 Sep-12 Daiichi Sankyo NR Sen Co., Ltd. 25 http://ClinicalTrials.gov/show/NCT01217008 http://ClinicalTrials.gov/show/NCT00680953 Impact of Pre-surgical Nasal Bacterial Reduction on Postoperative Surgical Site Infections Phase IV: Single group assignment NCT01148030 An Open-Label Long-Term Study Of Pregabalin For The Treatment Of Central Neuropathic Pain Phase III: Single group assignment, safety/efficacy study NCT01202227 Single Injection of REGN475/SAR164877 in Treatment of Vertebral Fracture Pain Phase II: RCT, efficacy study NCT01001715 Minocycline and Perfusion Pressure Augmentation in Acute Spinal Cord Injury Phase I/II: RCT, safety/efficacy study NCT00559494 Drug: 3M Skin and Nasal Antiseptic Surgical Site Infection; displaced hip fractures; spinal instability/fractures Drug: pregabalin Spinal Cord Diseases; Spinal Cord Injuries; Neuralgia; Pain Do Aromatase Inhibitors (AIs) Decrease Intestinal Calcium Absorption? Phase IV: Single group assignment, safety study NCT00766532 Rec 400 Child Jun-10 Jul-12 3M Adt Sen http://ClinicalTrials.gov/show/NCT01148030 Active, NR 100 Adt Sep-10 Mar-12 Pfizer Sen http://ClinicalTrials.gov/show/NCT01202227 Drug: Back Pain REGN475/SAR1648 77; Drug: Placebo Term 41 Adt Nov-09 Jan-11 Sanofi-Aventis; http://ClinicalTrials.gov/show/NCT01001715 Sen Regeneron Pharmaceuticals Drug: Minocycline; Drug: placebo; Procedure: SCPP augmentation; Procedure: SCPP control Spinal Cord Injuries Rec 60 Drug: Aromatase Inhibitor Breast Cancer; Osteoporosis; Osteopenia; Fracture; Fall Comp 11 Child Jun-04 Nov-10 University of http://ClinicalTrials.gov/show/NCT00559494 Adt Calgary; Sen Paralyzed Veterans of America; American Association of Neurological Surgeons; Hotchkiss Brain Institute, University of Calgary Child Jan-09 Oct-10 University of http://ClinicalTrials.gov/show/NCT00766532 Adt Wisconsin, Sen Madison Fonly 26 Efficacy in Reducing Fractures and Drug: Zoledronic acid Male Osteoporosis Safety of Zoledronic Acid in Men 5 mg iv; Drug: With Osteoporosis Placebo Phase III: RCT, safety/efficacy study NCT00439647 The Effect of PTH(1-84) or Drug: Parathyroid Back Pain Alendronate on Reduction of Back hormone (PTH) (1Pain in Postmenopausal Women 84); Drug: With an Osteoporosis Related Alendronate Vertebral Fracture(s) (FP-005-IM) Phase IV: RCT, safety/efficacy study NCT00713258 The Effect of PTH(1-84) or Drug: Parathyroid Back Pain Alendronate on Reduction of Back hormone (PTH) (1Pain in Postmenopausal Women 84); Drug: With an Osteoporosis Related Alendronate Vertebral Fracture(s) (FP-005-IM) Phase IV: RCT, safety/efficacy study NCT00713258 Effect of Teriparatide Compared to Drug: teriparatide; Osteoporosis, Risedronate on Back Pain in Drug: risedronate; Postmenopausal; Women With a Spine Fracture Drug: placebo; Drug: Back Pain; Spinal Caused by Osteoporosis placebo Fracture Phase III: RCT, efficacy study NCT00343252 Effect of Teriparatide Compared to Drug: teriparatide; Osteoporosis, Risedronate on Back Pain in Drug: risedronate; Postmenopausal; Women With a Spine Fracture Drug: placebo; Drug: Back Pain; Spinal Caused by Osteoporosis placebo Fracture Phase III: RCT, efficacy study NCT00343252 Procedure Comparing Surgical Decompression Versus Conservative Treatment in Incomplete Spinal Cord Injury RCT, efficacy study NCT01367405 Procedure: Surgical Central Spinal Cord decompression; Syndrome Procedure: Conservative treatment Comp 1199 Adt Dec-06 Oct-10 Novartis http://ClinicalTrials.gov/show/NCT00439647 Sen Pharmaceuticals Term 75 Adt Apr-08 Sep-10 Nycomed Sen http://ClinicalTrials.gov/show/NCT00713258 Fonly Term 75 Adt Apr-08 Sep-10 Nycomed Sen http://ClinicalTrials.gov/show/NCT00713258 Fonly Comp 712 Adt Jun-06 Jun-10 Eli Lilly and Sen Company http://ClinicalTrials.gov/show/NCT00343252 Fonly Comp 712 Adt Jun-06 Jun-10 Eli Lilly and Sen Company http://ClinicalTrials.gov/show/NCT00343252 Fonly Not yet Rec 72 27 Adt Jan-12 Jan-16 Radboud Sen University; Radboud University Medical Centre http://ClinicalTrials.gov/show/NCT01367405 Optimal Treatment for Spinal Cord Procedure: Early Spinal Cord Injury Injury Associated With Cervical surgery; Procedure: Canal Stenosis (OSCIS) Study Delayed surgery Phase I/II: RCT, safety/efficacy study NCT01485458 Evaluating Vertebroplasty and Procedure: Vertebral Body Kyphoplasty for Reducing Trauma- Kyphoplasty; Compression related Fractures Procedure: Fractures RCT, efficacy study Vertebroplasty NCT01402167 Vertebroplasty Compared With a Procedure: Osteoporotic Sham-procedure for Painful Acute Percutaneous Fractures Osteoporotic Vertebral Fractures vertebroplasty; Phase IV: RCT, efficacy study Procedure: Lidocaine NCT01537770 injection Vertebroplasty Compared With a Procedure: Osteoporotic Sham-procedure for Painful Acute Percutaneous Fractures Osteoporotic Vertebral Fractures vertebroplasty; Phase IV: RCT, efficacy study Procedure: Lidocaine NCT01537770 injection A Trial of Vertebroplasty for Painful Procedure: Osteoporosis; Acute Osteoporotic Vertebral percutaneous Vertebral Fracture Fractures vertebroplasty; Phase III: RCT, efficacy study Procedure: sham NCT01200277 procedure A Trial of Vertebroplasty for Painful Procedure: Osteoporosis; Acute Osteoporotic Vertebral percutaneous Vertebral Fracture Fractures vertebroplasty; Phase III: RCT, efficacy study Procedure: sham NCT01200277 procedure Surgical Versus Nonoperative Procedure: Surgical Metastatic Epidural Treatment of Metastatic Epidural excision of the Spinal Cord Spinal Cord Compression metastatic process; Compression Phase IV: Prospective, cohort Radiation: study Radiotherapy of the NCT00634426 metastatic spine process Rec 100 Adt Dec-11 Dec-14 Tokyo University http://ClinicalTrials.gov/show/NCT01485458 Sen Not yet Rec 30 Adt Mar-12 Mar-14 Centre http://ClinicalTrials.gov/show/NCT01402167 Sen Hospitalier Universitaire de Nīmes Rec 80 Rec 80 Rec 80 Adt Feb-12 Jan-14 Sygehus http://ClinicalTrials.gov/show/NCT01537770 Sen Lillebaelt; Odense University Hospital Adt Feb-12 Jan-14 Sygehus http://ClinicalTrials.gov/show/NCT01537770 Sen Lillebaelt; Odense University Hospital Adt Jan-11 Jan-14 St. Elisabeth http://ClinicalTrials.gov/show/NCT01200277 Sen Hospital, Tilburg, Netherlands Rec 80 Adt Jan-11 Jan-14 St. Elisabeth http://ClinicalTrials.gov/show/NCT01200277 Sen Hospital, Tilburg, Netherlands Rec 432 Adt Mar-08 Oct-13 AO Clinical http://ClinicalTrials.gov/show/NCT00634426 Sen Investigation and Documentation; AOSpine North America 28 The role of early surgery in patients paralysed following injury RCT ISRCTN61263382 Surgical Spinal Cord Injury decompression of compressed spinal cord and stabilisation: late vs early Procedure: Spinal Cord Injury Somatosensory reflex arch (Xiao Procedure) Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Clinical Outcome Single group assignment NCT01241630 A Controlled Trial of Vertebroplasty Procedure: for Acute Painful Osteoporotic Vertebroplasty Fractures RCT, efficacy study NCT01482793 A Controlled Trial of Vertebroplasty Procedure: for Acute Painful Osteoporotic Vertebroplasty Fractures RCT, efficacy study NCT01482793 Somato-sensory Reflex Arch in Spinal Cord Injury - Effect on Colorectal Transport Single group assignment NCT01274312 Evaluation of Wire Electrodes to Activate the Expiratory Muscles to Restore Cough Single group assignment, safety/efficacy study NCT00995215 Procedure: Xiao procedure Procedure: Spinal Cord Stimulation Active 328 Adt May-09 May-13 Sina Trauma http://www.controlledSen and Surgery trials.com/ISRCTN61263382 Research Centre (Iran) Rec 20 Adt Nov-09 Apr-13 University of Sen Aarhus; Lundbeck Foundation Vertebral Compression Fractures; Osteoporotic Vertebral Compression Fractures; Acute Vertebral Fractures Vertebral Compression Fractures; Osteoporotic Vertebral Compression Fractures; Acute Vertebral Fractures Spinal Cord Injuries Rec 120 Adt Nov-11 Apr-13 Optimus Clinical http://ClinicalTrials.gov/show/NCT01482793 Sen Research; Care Fusion Rec 120 Adt Nov-11 Apr-13 Optimus Clinical http://ClinicalTrials.gov/show/NCT01482793 Sen Research; Care Fusion Rec 20 Adt Nov-09 Apr-13 University of Sen Aarhus; Lundbeck Foundation Spinal Cord Injuries; Spinal Cord Diseases; Paralysis; Central Nervous System Diseases; Cough Rec 6 Adt Oct-09 Mar-13 Case Western http://ClinicalTrials.gov/show/NCT00995215 Sen Reserve University; National Institute of Neurological Disorders and Stroke (NINDS) 29 http://ClinicalTrials.gov/show/NCT01241630 http://ClinicalTrials.gov/show/NCT01274312 Spinal Cord Stimulation to Restore Procedure: Spinal Cough Cord Stimulation Single group assignment, safety/efficacy study NCT00116337 18 Adt Sep-04 Mar-13 Case Western http://ClinicalTrials.gov/show/NCT00116337 Sen Reserve University; National Institute of Neurological Disorders and Stroke (NINDS) Autologous Bone Marrow Stem Cell Transplantation in Patients With Spinal Cord Injury Phase I: Single group assignment, safety/efficacy study NCT01325103 Spinal Cord Injuries; Rec Spinal Cord Diseases; Paralysis; Central Nervous System Diseases; Cough; Trauma, Nervous System; Wounds and Injuries Procedure: Stem Cell Spinal Cord Injury Active, Transplantation NR 20 Adt Procedure: Conventional Treatment; Drug: Lithium Carbonate; Biological: Cord Blood Cell; Other: Placebo Procedure: Mantis; Procedure: XIA Spinal Cord Injury Rec 60 Vertebral Fracture Rec 100 Dorsal or dorsoventral stabilisation of spine fractures Spine fractures active 60 Adt Sep-09 Sep-12 Centre for Spinal http://www.controlledSurgery and trials.com/ISRCTN92182348 Brain Trauma, Germany Procedure: Discectomy with anular repair Diskectomy 750 Adt Mar-07 Jan-12 Anulex Sen Technologies, Inc. Lithium, Cord Blood Cells and the Combination in the Treatment of Acute & Sub-acute Spinal Cord Injury Phase I/II: RCT, safety/efficacy study NCT01471613 Identification of Microcirculation and Inflammation After Posterior Stabilization of the Spine RCT NCT01266200 Treatment of incomplete burst fractures (AO Type A3.1) with dorsal or dorso-ventral proceeding RCT, case-control ISRCTN92182348 Randomized Study of Anular Repair With the Xclose Tissue Repair System Phase IV: RCT, efficacy study NCT00760799 Active, NR 30 Jul-10 Jan-13 Hospital Sao http://ClinicalTrials.gov/show/NCT01325103 Rafael; Oswaldo Cruz Foundation; Irep Sociedade de Ensino Superior Médio e Fundamental Limitada; Hospital Espanhol Adt Sep-11 Dec-12 China Spinal http://ClinicalTrials.gov/show/NCT01471613 Cord Injury Network; Chengdu PLA General Hospital; StemCyte, Inc. Adt Dec-10 Dec-12 RWTH Aachen http://ClinicalTrials.gov/show/NCT01266200 Sen University http://ClinicalTrials.gov/show/NCT00760799 Evaluation of a Tongue Operated Procedure: Tongue Quadriplegia; Spinal Assistive Technology for Piercing; Device: Cord Injury; ALS Individuals With Severe Paralysis Usability assessment Phase I: Non-randomized, parallel assignment, safety/efficacy study NCT01124292 Cost Effectiveness and Efficacy of Kyphoplasty and Vertebroplasty Trial Phase III: RCT, safety/efficacy study NCT00279877 Cost Effectiveness and Efficacy of Kyphoplasty and Vertebroplasty Trial Phase III: RCT, safety/efficacy study NCT00279877 KAVIAR Study - Kyphoplasty And Vertebroplasty In the Augmentation and Restoration of Vertebral Body Compression Fractures Phase IV: RCT, safety/efficacy study NCT00323609 Transplantation of Autologous Olfactory Ensheathing Cells in Complete Human Spinal Cord Injury Phase I: Non-randomized, parallel assignment, safety/efficacy study NCT01231893 Rec 70 Adt May-10 Dec-11 Georgia Institute http://ClinicalTrials.gov/show/NCT01124292 of Technology; Shepherd Center; Northwestern University; Rehabilitation Institute of Chicago; University of Arizona Adt May-05 Aug-11 Mayo Clinic; http://ClinicalTrials.gov/show/NCT00279877 Sen Cardinal; ArthroCare Corporation; Cook Procedure: Kyphoplasty Osteoporotic Vertebral Compression Fractures Active, NR 112 Procedure: Kyphoplasty Osteoporotic Vertebral Compression Fractures Active, NR 112 Adt May-05 Aug-11 Mayo Clinic; Sen Cardinal; ArthroCare Corporation; Cook Procedure: Vertebroplasty; Procedure: Kyphoplasty Vertebral Body Compression Fractures Term 404 Adt Aug-06 Jul-11 Medtronic Spine http://ClinicalTrials.gov/show/NCT00323609 Sen LLC Rec 10 Child May-08 Oct-10 Wroclaw Medical http://ClinicalTrials.gov/show/NCT01231893 Adt University; Institute of Immunology and Experimental Therapy of the Polish Academy of Sciences; Department of Rehabilitation in Spinal Cord Injuries Akson Procedure: olfactory Complete Spinal mucosa ensheathing Cord Injuries cell grafting, rehabilitation; Other: rehabilitation 31 http://ClinicalTrials.gov/show/NCT00279877 Safety and Efficacy of Autologous Bone Marrow Stem Cells in Treating Spinal Cord Injury Phase I/II: Non-randomized, parallel assignment, safety/efficacy study NCT01186679 Quality of Life After Vertebroplasty Versus Conservative Treatment in Patients With Painful Osteoporotic Vertebral Fractures RCT, efficacy study NCT00994032 Quality of Life After Vertebroplasty Versus Conservative Treatment in Patients With Painful Osteoporotic Vertebral Fractures RCT, efficacy study NCT00994032 Surgical Management of Spinal Cord Injuries In Neck Phase II: RCT, safety/efficacy study NCT00475748 Procedure: laminectomy; Procedure: Intrathecal Anderson Circulating Tumor Cell Burden (CTCB) Study Phase IV: RCT, safety/efficacy study NCT00819832 Treatment for Acute Spinal Cord Injury Phase I/II: Single group assignment, safety/efficacy study NCT00695149 Functional Electrical Stimulation for Production of Artificial Cough Single group assignment NCT00589199 Spinal Cord Injuries Comp 12 Adt Procedure: Spinal Fracture; percutaneous Osteoporosis; Back injection of cement Pain into the vertebral body; Other: Medical treatment Procedure: Spinal Fracture; percutaneous Osteoporosis; Back injection of cement Pain into the vertebral body; Other: Medical treatment Procedure: Early and Central Cord late surgery for Syndrome; Spinal traumatic central Cord Injury; cord syndrome Quadriparesis Active, NR 100 http://ClinicalTrials.gov/show/NCT00994032 Active, NR 100 Active, NR 30 Procedure: Cancer; Spinal Kyphoplasty; Disease; Vertebral Procedure: Compression Vertebroplasty; Fractures Device: Cavity SpineWand Procedure: Spinal Cord Injury Transplantation of bone marrow stromal cell Term 3 Adt Mar-06 Jun-10 Hospital Clinic of Sen Barcelona; Sociedad Española de Radiologia Medica Adt Mar-06 Jun-10 Hospital Clinic of Sen Barcelona; Sociedad Española de Radiologia Medica Adt May-07 May-10 Maryland Sen Department of Health and Mental Hygiene; University of Maryland Adt Dec-08 May-10 M.D. Anderson Sen Cancer Center; ArthroCare Corporation Term 5 Child Jul-05 Mar-10 Translational Adt Research Informatics Center, Kobe, Hyogo, Japan http://ClinicalTrials.gov/show/NCT00695149 Procedure: Placement and use of the device Comp 5 Spinal Cord Injuries; Paralysis 32 Jan-08 Aug-10 International http://ClinicalTrials.gov/show/NCT01186679 Stemcell Services Limited Adt Dec-93 Jan-10 Case Western Reserve University; MetroHealth Medical Center http://ClinicalTrials.gov/show/NCT00994032 http://ClinicalTrials.gov/show/NCT00475748 http://ClinicalTrials.gov/show/NCT00819832 http://ClinicalTrials.gov/show/NCT00589199 Other C-STOP Fracture Trial Phase III: RCT, safety/efficacy study NCT01401556 Other: case Osteoporosis management; Other: Multifaceted quality improvement intervention To Study the Safety and Efficacy Other: Autologous Spinal Cord Injury of Autologous Bone Marrow Stem Bone Marrow derived Cells in Patients With Spinal Cord Stem Cells Injury Phase I/II: Single group assignment, safety/efficacy study NCT01490242 Nuclear MRI(NMR)in Women at Radiation: Virtual Osteoporosis, Risk of Fracture Receiving Either Bone Biopsy by Osteopenia Zoledronic Acid or Teriparatide Magnetic Resonance RCT, efficacy study Imaging NCT01153425 Comparison of Balloon Kyphoplasty, Vertebroplasty and Conservative Management in Acute Osteoporotic Vertebral Fractures RCT, safety/efficacy study NCT00749060 Comparative Study of Balloon Kyphoplasty and Conservative Treatment Phase IV: RCT, safety/efficacy study NCT00749242 Other: conventional treatment; Procedure: kyphoplasty with balloons; Procedure: vertebroplasty Osteoporotic Vertebral Fracture; Between T5 and L5; of Less Than 6 Weeks Duration Other: orthopedic SPINAL Fracture corset; Device: balloon kyphoplasty Not yet 220 Rec Adt Sen Jul-11 Jul-15 University of Alberta Oct-11 Oct-13 TotipotentRX Cell Therapy Pvt. Ltd.; Fortis Healthcare http://ClinicalTrials.gov/show/NCT01401556 Rec 15 Adt Active, NR 56 Adt Sen 200 Adt Dec-07 Dec-12 Assistance http://ClinicalTrials.gov/show/NCT00749242 Sen Publique Hôpitaux de Paris; Ministry of Health, France Rec Rec http://ClinicalTrials.gov/show/NCT01490242 Jul-08 Jun-13 University of http://ClinicalTrials.gov/show/NCT01153425 Pennsylvania; Eli Lilly and FCompany; only Novartis Pharmaceuticals 300 Adt Dec-07 Dec-12 Assistance http://ClinicalTrials.gov/show/NCT00749060 Sen Publique Hôpitaux de Paris; Ministry of Health, France 33 The Effects of Two Functional Other: Cycling with Electrical Stimulation Cycling functional electrical Paradigms stimulation Phase II/III: RCT, efficacy study NCT01244594 Spinal Cord Injury Rec 20 Adt Jul-10 Jul-12 University of the http://ClinicalTrials.gov/show/NCT01244594 Sciences in Philadelphia; The Craig H. Neilsen Foundation; Thomas Jefferson University; Magee Rehabilitation Hospital; Temple University; University of Delaware Active, 2000 Adt Jun-08 Dec-11 University of http://ClinicalTrials.gov/show/NCT00594789 NR Sen Manitoba; The Manitoba Patient Access Network Steering Committee; The Manitoba Bone Density Program Committee Active, 180 Adt May-08 Jul-11 University of http://ClinicalTrials.gov/show/NCT00866112 NR Kansas Closing The Post Fracture Care Gap In Manitoba RCT NCT00594789 Other: Information letters Osteoporosis A Randomized Exercise Trial for Wheelchair Users RCT, efficacy study NCT00866112 Other: Educational session to promote physical activity; Other: Minimal contact The Prevalence of Osteoporotic Vertebral Compression Fractures (OVCF) in Korean Post Menopausal Women Cross-sectional study NCT01381588 Radiological Biological Genetic and Micro-architectural Bone Determinants of Fractures in Men With Low Bone Mineral Density Non-randomized, parallel assignment NCT01250314 Other: Fracture evaluation Spinal Cord Injury; Multiple Sclerosis; Muscular Dystrophy; Cerebral Palsy; Spina Bifida; Amputation; Arthritis; Stroke Osteoporosis, Comp 1136 Adt Oct-10 Feb-11 GlaxoSmithKline http://ClinicalTrials.gov/show/NCT01381588 Postmenopausal Sen Fonly Other: Radiology; Other: Biological, biochemical and genetic samples Osteoporosis Rec 200 34 Adt Feb-08 Feb-11 Assistance http://ClinicalTrials.gov/show/NCT01250314 Sen Publique Hôpitaux de Paris; Ministry of Health, France Miscellaneous observational studies Study of Sacral Fractures Using Patient Based and Objective Outcomes Prospective, cohort study NCT00798733 Utility of CT Fluoroscopy Guidance During Percutaneous Sacroplasty With Quality of Life Assessment Prospective, case-only study NCT00765258 Characterization of At-risk Population for Pre-sacral Tumor in CURRARINO Syndrome Prospective, cohort study NCT00780117 High-Resolution Diffusion Tensor Imaging (DTI) of the Cervical Spinal Cord in the Setting of Spinal Cord Injury (SCI) Prospective, case control study NCT01407705 The Natural History of Traumatic Spinal Cord Injury Using fMRI, MRS and DTI Prospective, cohort study NCT00790361 Evaluation of Circulating Osteogenic Factors in Trauma Patients Cross-sectional, cohort study NCT01433536 Sacrum Fracture Rec Sacro-Iliac Insufficiency Fractures Rec 1000 Adt Oct-08 Dec-14 Boston Medical http://ClinicalTrials.gov/show/NCT00798733 Sen Center; Foundation of Orthopedic Trauma 100 Adt Jan-08 Dec-14 Medical College http://ClinicalTrials.gov/show/NCT00765258 Sen of Wisconsin; Montefiore Medical Center CURRARINO Rec Syndrome; Sacrococcygeal Teratoma; Presacral Mass Spinal Cord Injury; Invite Cervical Spondylosis With Myelopathy; Degenerative Disorder 80 Child Jun-08 Sep-14 Assistance Adt Publique Sen Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT00780117 70 Adt May-07 Feb-13 University of Sen Utah http://ClinicalTrials.gov/show/NCT01407705 Central Cord Syndrome Not yet Rec 20 Rec 60 Adt Jan-12 Jan-13 Lawson Health http://ClinicalTrials.gov/show/NCT00790361 Sen Research Institute; The Physicians' Services Incorporated Foundation Adt Dec-10 Sep-11 Centre http://ClinicalTrials.gov/show/NCT01433536 Hospitalier Universitaire de Sherbrooke; Universitaire de Sherbrooke; Canadian Institutes of Health Research Healthy; High Velocity Fracture; Cranial Trauma; Spinal Trauma 35 A3C: OTHER Title Phases: trial design (control) CT ID Behavioural Short Versus Long Post-Operative Restrictions Following Lumbar Discectomy RCT, efficacy study NCT01363830 Interventions Cognitive-Behavioral Physical Therapy Intervention Phase I/II: RCT, efficacy study NCT01131611 Helping Patients With Spinal Stenosis Make a Treatment Decision: A Randomized Study Assessing The Benefits of Health Coaching RCT NCT01263678 Function After Spinal Treatment, Exercise and Rehabilitation: Improving the functional outcome of spinal surgery RCT ISRCTN46782945 Behavioral: CBPT; Other: Physical Therapy Device Evaluate Initial Safety of the HemiBridge™ System in Guided Spinal Growth Treatment of Progressive Idiopathic Scoliosis Single group assignment, safety study NCT01465295 Conditions Recruit n Rec 420 Not yet Rec 70 Behavioral: Post DA Spinal Stenosis viewing coaching; Other: Usual Care Invite Rehabilitation Programme; Exercise booklet Behavioral: TwoLumbar Disc Week Post-Operative Herniation Restriction; Behavioral: SixWeek Post-Operative Restriction Spinal Stenosis Spinal lateral root stenosis and discectomy Device: Mechanical Scoliosis hemiepiphysiodesis using the HemiBridge System Age Start (Grp) Date End Sponsors Date URL Adt Aug-09 Dec-13 Brigham and Sen Women's Hospital; Massachusetts General Hospital; Beth Israel Deaconess Medical Center Adt Jan-12 Aug-13 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT01363830 200 Adt Nov-10 Nov-11 DartmouthSen Hitchcock Medical Center http://ClinicalTrials.gov/show/NCT01263678 Comp 344 Adt Apr-05 Mar-10 Arthritis Sen Research Campaign (ARC) (UK) http://www.controlledtrials.com/ISRCTN46782945 Rec 6 36 http://ClinicalTrials.gov/show/NCT01131611 Child Aug-11 Jan-21 SpineForm LLC; http://ClinicalTrials.gov/show/NCT01465295 Adt Children's Sen Hospital Medical Center, Cincinnati; University Hospital Case Medical Center Safety and Performance of the Elaspine System in the Treatment of the Lumbar Spine Single group assignment, safety/efficacy study NCT01323543 Minuteman Spinal Fusion Implant Versus Surgical Decompression for Lumbar Spinal Stenosis Phase IV: RCT, safety/efficacy study NCT01455805 Condition of Approval Study Phase IV: Single group assignment, safety/efficacy study NCT00517751 INFUSE®Bone Graft in Transforaminal Lumbar Interbody Fusion for Degenerative Disease of Lumbosacral Spine Phase III: Non-randomized, parallel assignment, safety/efficacy study NCT01415908 Intra-Operative Dural Brachytherapy With Yttrium-90 Plaque Applicators Single group assignment, safety/efficacy study NCT00706485 Device: Elaspine™ Lower Back Pain Rec 40 Device: Minuteman Interspinous Interlaminar Fusion Implant; Procedure: surgical decompression Device: X-STOP PEEK Lumbar Spinal Stenosis; Spondylolisthesis; Degenerative Disc Disease Lumbar Spinal Stenosis Rec 240 Adt Aug-07 Dec-18 Medtronic Spine http://ClinicalTrials.gov/show/NCT00517751 Sen LLC Device: INFUSE Bone Graft; Other: Iliac Crest Bone Graft Lumbar Spine Degeneration Rec 534 Adt Sen Jul-11 Device: Yttrium-90 Plaque Applicator Spinal Neoplasms Susp 10 Adt Sen Jul-07 Spinal Cord Stimulation With Precision® SCS System Versus Reoperation for Failed Back Surgery Syndrome Phase IV: RCT, efficacy study NCT01036529 Device: Precision Spinal Cord Stimulation; Procedure: Back Surgery Failed Back Surgery Syndrome; Leg Pain; Back Pain; Spinal Cord Stimulation Rec 132 Not yet 180 Rec 37 Adt Aug-10 Dec-20 Spinelab AG; Sen MDT Medical Device Testing GmbH http://ClinicalTrials.gov/show/NCT01323543 Adt Jan-12 Dec-19 Spinal Simplicity http://ClinicalTrials.gov/show/NCT01455805 Sen LLC; The Leeds Teaching Hospitals NHS Trust Jul-17 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01415908 and Biologics Jul-17 Massachusetts http://ClinicalTrials.gov/show/NCT00706485 General Hospital; National Institutes of Health; Implant Sciences Adt Feb-10 Mar-17 Boston Scientific http://ClinicalTrials.gov/show/NCT01036529 Sen Corporation Effect of Human Thrombin With Gelatin Matrix on Perioperative Blood Loss in Scoliosis Surgery Phase IV: RCT, efficacy study NCT01451788 Device: Gelatin matrix with human derived thrombin (Floseal, Baxter) Adolescent Idiopathic Scoliosis Dynesys Spinal System Post Market 522 Study Efficacy study NCT01528072 A Clinical Study of the Dynesys(R) Spinal System Phase III: RCT, safety/efficacy study NCT00759057 DuraSeal Exact Spine Sealant System Post-Approval Study Phase IV: Cohort study NCT01410864 Kineflex/C Artificial Disc System to Treat Cervical Degenerative Disc Disease (DDD) RCT, safety/efficacy study NCT00374413 Comparison of the Aspen Device Versus Pedicle Screws for Supplemental Posterior Fixation in Lumbar Interbody Fusion Phase IV: RCT, efficacy study NCT01549366 Kineflex Artificial Disc System to Treat Degenerative Disc Disease (DDD) RCT, safety/efficacy study NCT00292292 Device: Dynesys Spinal System Degenerative Spondylolisthesis; Pseudoarthrosis Rec 60 Child Nov-11 Dec-16 Turku University http://ClinicalTrials.gov/show/NCT01451788 Adt Hospital; Tampere University Hospital; Helsinki University Central Hospital Not yet 168 Adt Mar-12 Mar-16 Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01528072 Rec Sen Device: Posterior Pedicle Screw System Degenerative Active, 399 Spondylolisthesis or NR Retrolisthesis; Spinal Stenosis; Stenosing Lesion. Device: DuraSeal Dural Sealing Not yet 1044 Exact Spine Sealant Rec System; Other: Control Device: Artificial disk; Degenerative Disc Active, 343 Device: Artificial disc Disease (DDD) NR Adt Mar-03 Dec-15 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT00759057 Adt Aug-11 Sep-15 Covidien Sen http://ClinicalTrials.gov/show/NCT01410864 Adt http://ClinicalTrials.gov/show/NCT00374413 Device: Aspen Spinous Process Fixation Device; Device: Pedicle Screw Fixation Degenerative Disc Disease (DDD) Rec 144 Adt Feb-12 May-15 Lanx, Inc. Sen http://ClinicalTrials.gov/show/NCT01549366 Device: Lumbar Artificial Disc; Device: Charite Artificial Disc Degenerative Disc Disease Active, NR 514 Adt http://ClinicalTrials.gov/show/NCT00292292 38 Jul-05 Aug-15 SpinalMotion Jan-05 Mar-15 SpinalMotion Study of the Safety and Device: DIAM™ Effectiveness of DIAM™ Spinal Spinal Stabilization Stabilization System Versus System; Procedure: Conservative Care Conservative care Phase III: RCT, safety/efficacy study NCT00456378 The iO-Flex® Study: Evaluation of Device: Baxano iOthe Baxano iO-Flex® System for Flex® System Decompressive Lumbar Surgery Prospective, case-only study NCT01067014 Performance of Inductigraft in Device: Inductigraft Spinal Fusion Phase IV: Single group assignment, safety/efficacy study NCT01452022 Trial Assessing Cooled Device: Sinergy; Radiofrequency Denervation as a Device: Placebo Treatment for Sacroiliac Joint Pain sham Using the Sinergy System RCT, efficacy study NCT00802997 Wallis Stabilization System for Low Interspinous process Back Pain & dynamic Phase III: RCT, safety/efficacy stabilization (Wallis study System); Total Disc NCT00484458 Replacement Proximal Junctional Kyphosis Device: Semi rigid Following Long Instrumented rod; Device: Rigid Spinal Fusion: The Effect of Rod Implant Selection Phase IV: RCT, efficacy study NCT01441999 A Postmarket Surveillance Study Device: Dynamic of the Paradigm Spine Dynamic Stabilization System Stabilization System (DSS) (DSS) Single group assignment, safety study NCT01461005 Rec 306 Adt Dec-06 Feb-15 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00456378 Sen and Biologics Invite 75 Adt Feb-10 Dec-14 Baxano, Inc. Sen http://ClinicalTrials.gov/show/NCT01067014 Degenerative Disk Disease; Spinal Stenosis of Lumbar Region Rec 230 Adt Oct-11 Dec-14 Apatech, Inc. Sen http://ClinicalTrials.gov/show/NCT01452022 Sacroiliac Pain Rec 51 Adt Jun-08 Dec-14 Coastal http://ClinicalTrials.gov/show/NCT00802997 Sen Orthopedics & Sports Medicine Low Back Pain Active, NR 340 Adt Junctional Kyphosis Not yet Rec 24 Adt Oct-11 Sep-14 Globus Medical http://ClinicalTrials.gov/show/NCT01441999 Sen Inc (US) Spondylolisthesis; Neurologic Deficits; Kyphosis; Pseudarthrosis 150 Adt Sep-11 Jul-14 Paradigm Spine; http://ClinicalTrials.gov/show/NCT01461005 Sen Musculoskeletal Clinical Regulatory Advisers LLC Lumbar Degenerative Disc Disease Lumbar Spinal Stenosis Rec 39 Jan-07 Nov-14 Zimmer Spine; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00484458 A Prospective, Randomized, Multicenter Study to Demonstrate the Superiority of the Barricaid to Discectomy for Primary Lumbar Disc Herniation Phase IV: RCT NCT01283438 Clinical Trial Comparing Decompression With and Without Coflex™ Treating Lumbar Spinal Stenosis RCT, safety/efficacy study NCT01316211 SMART Clinical Study: Surgical Multi-center Assessment of RF Ablation for the Treatment of Vertebrogenic Back Pain RCT, safety/efficacy study NCT01446419 Scoliosis Surgery Using the PASS® LP System Phase IV: Single group assignment, safety/efficacy study NCT01019109 Trial Evaluating the Safety and Effectiveness of NUBAC™ Disc Arthroplasty RCT, safety/efficacy study NCT00931515 Bone Graft Materials Observational Registry Prospective, cohort study NCT00974623 Device: Barricaid; Lumbar Disc Device: Standard of Herniation Care Rec 400 Adt Dec-10 May-14 Intrinsic Sen Therapeutics Device: Implantation Spinal Stenosis of coflex™ after surgical decompression; Procedure: Surgical decompression Device: Intracept Low Back Pain Treatment; Device: Intracept Treatment Rec 230 Adt Jun-07 May-14 Paradigm Spine; http://ClinicalTrials.gov/show/NCT01316211 Sen MDT Medical Device Testing GmbH Rec 200 Adt Oct-11 Apr-14 Relievant Sen Medsystems, Inc. Device: Posterior Idiopathic Scoliosis Spinal Fusion Device Rec 120 Child May-10 Mar-14 Medicrea, USA Adt Corp. Sen Device: NUBAC™ vs Degenerative Disc ProDisc™ Disease Active, NR 400 Adt Feb-09 Feb-14 Pioneer Surgical http://ClinicalTrials.gov/show/NCT00931515 Sen Technology, Inc. Rec 300 Adt Sep-09 Dec-13 Apatech, Inc. Sen Device: Bone graft Degenerative Disc substitute, autograft Disease; Herniated or allograft Disc; Spinal Stenosis; Spondylolithesis; Spinal Deformity; Cervical Myelopathy; Failed Back Surgery Syndrome; Spinal Cord Neoplasms 40 http://ClinicalTrials.gov/show/NCT01283438 http://ClinicalTrials.gov/show/NCT01446419 http://ClinicalTrials.gov/show/NCT01019109 http://ClinicalTrials.gov/show/NCT00974623 Efficacy and Safety of Accell Evo3 DBM in Instrumented Posterolateral Lumbar Spine Fusion Single group assignment, safety/efficacy study NCT01430299 Investigating Superion™ In Spinal Stenosis [ISISS] RCT, safety/efficacy study NCT00692276 Device: Integra Accell Evo3 Stenosis; Spondylosis; Degenerative Changes Rec 30 Adt Jun-11 Dec-13 Integra Sen LifeSciences Corporation http://ClinicalTrials.gov/show/NCT01430299 Device: Superion™ Interspinous Spacer; Device: X-STOP® IPD® Device Lumbar Spinal Stenosis; Neurogenic Intermittent Claudication Lumbar Spinal Stenosis Rec 400 Adt Jun-08 Dec-13 VertiFlex, Sen Incorporated http://ClinicalTrials.gov/show/NCT00692276 Rec 300 Adt Oct-06 Oct-13 Facet Solutions, http://ClinicalTrials.gov/show/NCT00401518 Sen Inc. Active, NR 45 Adt Apr-09 Aug-13 Intrinsic Sen Therapeutics A Pivotal Study of a Facet Device: Facet Replacement System to Treat Arthroplasty Spinal Stenosis Phase III: RCT, safety/efficacy study NCT00401518 Barricaid EU Post Market Study for Device: Barricaid Lumbar Disc Primary Lumbar Disc Herniation Herniation Phase IV: Single group assignment NCT01534065 Prospective, Multi-Center Clinical Device: chronOS Degenerative Disc Outcomes Study Evaluating the strip Disease With or chronOS Strip Combined With Without Stenosis Bone Marrow Aspirate Single group assignment NCT00943384 Study Of The Efficacy Of Device: Neurotome Low Back Pain Neurolysis In Functional Recovery OFF; Procedure: From Chronic Nonspecific Low neurolysis Back Pain RCT, efficacy study NCT01190033 Study of Bioactive Glass-ceramic Device: 4 CIS one- Degenerative Disk Intervertebral Spacer (Bonglass- touch titanium cage; Disease SS) in Posterior Lumbar Interbody Device: Bonglass-SS Fusion SSLPB RCT, efficacy study NCT01439464 Active, NR Monly 102 Adt Jul-09 Sen Jul-13 Synthes USA HQ, Inc. http://ClinicalTrials.gov/show/NCT01534065 http://ClinicalTrials.gov/show/NCT00943384 Rec 40 Adt Aug-10 Jul-13 University of Sao http://ClinicalTrials.gov/show/NCT01190033 Paulo Rec 86 Adt Oct-10 Jun-13 BioAlpha Inc. Sen 41 http://ClinicalTrials.gov/show/NCT01439464 Post-Operative Colonization Rates of Femoral Nerve Catheters Treated With ChlorhexidineImpregnated Patch Phase IV: RCT, safety study NCT01411891 Device: Chlorhexidine impregnated patch (Biopatch) Spine Reference Parameters on Device: EOS™ EOS Imaging Acquisition Prospective, cohort study NCT01406743 Safety and Efficacy of the Device: TransDiscal TransDiscal System Versus System; Other: Medical Management in Treating Medical Chronic Discogenic Low Back Pain Management Phase IV: RCT, safety/efficacy study NCT01263054 Salient Aquamantys Spine Trial Device: Bipolar Phase IV: RCT, efficacy study Sealer NCT01331499 (Aquamantys); Procedure: Standard of Care Herniectomy Versus Herniectomy Device: DIAM™ With a Spinal Stabilization System Spinal Stabilization for the Treatment of Complex Disc System; Procedure: Disease Herniectomy Phase IV: RCT, efficacy study NCT00749996 LDR Spine USA Mobi-C(R) Device: Cervical Cervical Disc Prosthesis IDE Artificial Disc Phase II: RCT, safety/efficacy study NCT00389597 Evaluation of an 3D Imaging Device: Navigation Intensifier Coupled to a Navigation station coupled with Station in the Surgery of the Spine a 3D fluoroscopy and Pelvis Phase III: RCT, safety/efficacy study NCT01335841 Catheter Infections; Spinal Catheter (Epidural) (Subdural); Complications, Infection or Inflammation Healthy Volunteers Rec 100 Adt Aug-11 Jun-13 University of Sen Wisconsin, Madison http://ClinicalTrials.gov/show/NCT01411891 Rec 204 Adt May-11 May-13 University Sen Hospital, Bordeaux http://ClinicalTrials.gov/show/NCT01406743 Back Pain Rec 136 Adt Dec-10 May-13 Kimberly-Clark Sen Corporation http://ClinicalTrials.gov/show/NCT01263054 Blood Loss Rec 128 Adt Apr-11 Apr-13 Salient Surgical http://ClinicalTrials.gov/show/NCT01331499 Sen Technologies Sciatica; Lumbar Degenerative Disc Disease Active, NR 165 Adt Nov-06 Apr-13 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00749996 & Biologics ECA Degenerative Disc Disease Active, NR 600 Adt Apr-06 Mar-13 LDR Spine USA http://ClinicalTrials.gov/show/NCT00389597 Sen Rec 150 Adt Mar-11 Mar-13 AdministrateurCI http://ClinicalTrials.gov/show/NCT01335841 Sen C; PRAXIM company Surgical Procedure, Unspecified 42 Clinical Outcomes of the Trinica(R) Device: Trinica Degenerative Disc Anterior Lumbar Plate: Fixed Anterior Lumbar Disease; Spinal Screws vs. Variable Screws Plate System Stenosis; RCT Spondylolisthesis NCT00762723 Senza™ spinal cord stimulation Senza™ spinal cord Chronic back and system for the treatment of chronic stimulation system leg pain in failed back and leg pain in failed back back surgery surgery syndrome (FBSS) patients syndrome (FBSS) RCT patients ISRCTN33292457 SS) patients The Use of Dermabond Versus Device: 2Wounds Standard Staple for Wound octylcyanoacrylate Closure in Children With (Dermabond) Neuromuscular Scoliosis closure; Device: Undergoing Spinal Deformity Standard staple Correction Surgery closure Phase II: RCT, safety/efficacy study NCT01135940 Freedom Lumbar Disc in the Device: FLD; Device: Degenerative Disc Treatment of Lumbar Degenerative Control Disease (DDD) Disc Disease RCT, safety/efficacy study NCT00775801 INFUSE® Bone Graft/ PEEK Device: INFUSE® Degenerative Disc Interbody Spacer/ Anterior Cervical Bone Graft/PEEK Disease Plate Pivotal Clinical Trial Spacer/Anterior Phase III: Single group Cervical Plate assignment, safety/efficacy study NCT00485173 Efficacy of the Aspen Spinous Device: Aspen Degenerative Disc Process System in Anterior Spinous Process Disease Lumbar Interbody Fusion (ALIF) System; Device: Phase IV: RCT Pedicle Screw NCT01016314 Fixation Active, NR 120 Child Feb-08 Feb-13 Zimmer, Inc. Adt Sen http://ClinicalTrials.gov/show/NCT00762723 Active 20 Adt Apr-11 Dec-12 Nevro Sen Corporation (USA) http://www.controlledtrials.com/ISRCTN33292457 Rec 80 Child May-10 Dec-12 University of http://ClinicalTrials.gov/show/NCT01135940 Adt British Columbia; BCCH Telethon Grant Rec 300 Adt Sep-08 Dec-12 AxioMed Spine Corporation Active, NR 225 Adt Jun-07 Dec-12 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00485173 Sen and Biologics Rec 156 Adt Nov-09 Nov-12 Lanx, Inc. Sen 43 http://ClinicalTrials.gov/show/NCT00775801 http://ClinicalTrials.gov/show/NCT01016314 Safety and Effectiveness Study of Device: AO-1000 Disk, Herniated the AO-1000 Device to Treat Contained Herniated Discs Phase I: Single group assignment, safety/efficacy study NCT01339377 Pilot Study to Assess Device: Prefix Degenerative Disc Safety/Preliminary Effectiveness of (AMPLEX) B2A Disease; Prefix in Subjects With Peptide Enhanced Spondylolisthesis Degenerative Disc Disease (DDD) Ceramic Granules; Undergoing Spine Fusion Surgery Other: Iliac crest Phase I/II: RCT, safety/efficacy autograft study NCT00798902 Comparison of Standard Fusion Device: Topping off Spondylolisthesis; With “Topping Off”-System in system; Device: Erosive Lumbar Spine" monosegmental PLIF Osteochondrosis in RCT, safety/efficacy study L2-S1 NCT01224379 Mild® Decompression Alternative Device: mild® Lumbar Spinal to Open Surgery Epidural Steroid Lumbar Stenosis Injection Comparative Outcomes Decompression; Study Drug: Epidural RCT Steroid Injection NCT01315145 Adjunctive Biofeedback Device: StressEraser Post-traumatic Intervention for Operation Iraqi Stress Disorder Freedom/Operation Enduring Freedom (OIF-OEF) Post Traumatic Stress Disorder (PTSD) RCT, efficacy study NCT00920036 Cervical Spine; Movement Before Device: Activ C disc Diskectomy; and After Anterior Cervical prosthesis; Intervertebral Disk Discectomy, With or Without a Procedure: Anterior Displacement Cervical Disc Prosthesis cervical discectomy RCT, efficacy study NCT00868335 Rec 40 Adt Aug-11 Oct-12 ActiveO Inc. Sen http://ClinicalTrials.gov/show/NCT01339377 Active, NR 22 Adt Nov-08 Oct-12 BioSurface Sen Engineering Technologies, Inc http://ClinicalTrials.gov/show/NCT00798902 Not yet Rec 30 Adt Jan-11 Oct-12 University of Sen Cologne http://ClinicalTrials.gov/show/NCT01224379 Rec 200 Adt Mar-11 Sep-12 Vertos Medical, http://ClinicalTrials.gov/show/NCT01315145 Sen Inc. Active, NR 30 Adt Feb-10 Sep-12 Department of http://ClinicalTrials.gov/show/NCT00920036 Sen Veterans Affairs Rec 24 Adt Dec-07 Aug-12 Maastricht http://ClinicalTrials.gov/show/NCT00868335 University Medical Center; B. Braun/ Aesculap Spine 44 Efficacy Study of the Octapolar Device: Octad® lead Lead in Patients With Failed Back (Spinal cord Surgery Syndrome (FBSS) With stimulation) Chronic Pain Phase IV: Single group assignment, safety/efficacy study NCT01096147 Blue Light Device for Pain Therapy Device: Pain Relief Phase III: RCT, efficacy study Patch; Device: NCT01528332 Control PRP device Pilot Study to Assess Safety/Prelimary Effectiveness of Prefix in Subjects With Degenerative Disc Disease (DDD) Undergoing Spine Fusion Surgery Phase I/II: RCT, safety/efficacy study NCT00798239 Failed Back Surgery Syndrome Rec Low Back Pain; Low Rec Back Pain, Recurrent; Musculoskeletal Pain; Chronic Pain Degenerative Disc Active, Disease; NR Spondylolisthesis Device: Prefix (AMPLEX) B2A Peptide Enhanced Ceramic Granules; Other: Iliac crest autograft; Device: Prefix (AMPLEX) B2A Peptide Enhanced Ceramic Granules XL TDR® eXtreme Lateral Total Device: XL TDR; Degenerative Disc Disc Replacement for the Other: Lumbar fusion Disease Treatment of Lumbar Degenerative surgery Disc Disease (DDD) Phase III: Single group assignment, safety/efficacy study NCT00927238 PSU Lumbar Support for Device: PSU lumbar Low Back Pain Prevention of Low Back Pain in back support Rubber Tapper Phase III: RCT, efficacy study NCT01017588 CNAP™ Monitor Study Device: CNAP Cardiac Surgery; Prospective, case-only study Spinal Surgery NCT01356082 300 Adt Feb-10 Aug-12 Medtronic Sen Neuromodulation Europe http://ClinicalTrials.gov/show/NCT01096147 170 Adt Feb-12 Aug-12 Light and Health http://ClinicalTrials.gov/show/NCT01528332 Venture 24 Adt Nov-08 Jul-12 BioSurface Sen Engineering Technologies, Inc 300 Adt Sen http://ClinicalTrials.gov/show/NCT00798239 Jul-12 NuVasive http://ClinicalTrials.gov/show/NCT00927238 Not yet 200 Child Jan-10 Jun-12 Prince of Rec Adt Songkla University http://ClinicalTrials.gov/show/NCT01017588 Rec Invite Jul-09 100 Child May-11 Apr-12 Nationwide Adt Children's Hospital 45 http://ClinicalTrials.gov/show/NCT01356082 Wallis Mechanical Normalization Device: Interspinous Low Back Pain System for Low Back Pain process and dynamic Phase III: RCT, safety/efficacy stabilization; Device: study Conservative Care NCT00134537 Masimo Radical-7 Monitor a Useful Device: Masimo Major Spine Surgery Adjuvant During Major Spine Radical-7 Procedure Surgery Prospective study NCT01221961 MiDAS II (Mild® Decompression Device: mild® Lumbar Spinal Alternative to Open Surgery): Interlaminar Stenosis Vertos Mild Patient Evaluation Decompression Study Phase IV: Single group assignment NCT01082159 Safety and Efficacy of MRgFUS for Device: Exablate Lower Back Pain, the Treatment of Low Back Pain treatment Facets Joints Phase II: Single group Osteoarthritis assignment, safety/efficacy study NCT01232582 MiDAS I (Mild® Decompression Device: MILD® Lumbar Spinal Alternative to Open Surgery): Interlaminar Stenosis Vertos Mild Patient Evaluation Decompression Study Phase IV: Single group assignment NCT00956631 Ultrasound as Adjunct Therapy for Device: Exogen Lumbar Increasing Fusion Success After Bone Healing Degenerative Disc Lumbar Surgery System; Device: Disease Phase III: RCT, safety/efficacy Exogen Bone study Healing System NCT00744861 Clinical Trial to Evaluate Safety Device: Hyalospine Degenerative Spinal and Efficacy of Hyalospine® in Stenosis; Disk Lumbar Laminectomy or Herniation Laminotomy Phase II/III: RCT, safety/efficacy study NCT00939406 Active, NR 300 Adt Nov-04 Apr-12 Zimmer Spine; Zimmer, Inc. Rec 100 Adt Oct-10 Apr-12 Cedars-Sinai http://ClinicalTrials.gov/show/NCT01221961 Sen Medical Center; Masimo Corporation Active, NR 55 Adt Feb-10 Apr-12 Vertos Medical, http://ClinicalTrials.gov/show/NCT01082159 Sen Inc. Comp 50 Adt Oct-09 Feb-12 InSightec Sen Active, NR 78 Adt Sen Rec 400 Adt Sep-08 Dec-11 Smith & Sen Nephew, Inc. Rec 50 Adt Nov-09 Dec-11 AO Clinical http://ClinicalTrials.gov/show/NCT00939406 Sen Investigation and Documentation 46 http://ClinicalTrials.gov/show/NCT00134537 http://ClinicalTrials.gov/show/NCT01232582 Jul-08 Jan-12 Vertos Medical, http://ClinicalTrials.gov/show/NCT00956631 Inc. http://ClinicalTrials.gov/show/NCT00744861 A Study of the In-Space Device for Treatment of Moderate Spinal Stenosis Phase III: RCT, safety/efficacy study NCT00697827 Comparison Between Return and Wastage of Your Own Blood, Collected During Spinal Surgery, for Verification of Safety When Returning Blood RCT, safety study; NCT01251042 Safety and Effectiveness Study of Prodisc to Spinal Fusion Surgery RCT, safety/efficacy study NCT00295009 Spine Research With Roentgen Stereophotogrammetric Analysis Phase IV: Single group assignment, efficacy study NCT00493558 Effects of X-STOP® Versus Laminectomy Study Phase IV: RCT, safety/efficacy study NCT00558129 Predicting Outcome of Transcutaneous Electrical Nerve Stimulator (TENS) in Failed Back Surgery Syndrome RCT, safety/efficacy study NCT01185665 Device: Interspinous Spinal Stenosis Spacer device; Device: Interspinous Process Distraction Device Active, NR 500 Adt Jun-08 Dec-11 Synthes USA Sen HQ, Inc. http://ClinicalTrials.gov/show/NCT00697827 Device: Sangvia Spinal Surgery Comp 51 Adt Oct-10 Dec-11 Astra Tech AB Sen http://ClinicalTrials.gov/show/NCT01251042 Device: Total disc replacement Spinal Diseases Active, NR 510 Adt Sep-01 Dec-11 Synthes USA HQ, Inc. http://ClinicalTrials.gov/show/NCT00295009 Active, NR 25 Adt Sen Wdrwn 0 Adt Nov-07 Nov-11 Medtronic Spine http://ClinicalTrials.gov/show/NCT00558129 Sen LLC Device: TENS; Failed Back Surgery Not yet Device: Sham-TENS Syndrome Rec 40 Adt Sep-10 Sep-11 Universitair Sen Ziekenhuis Brussel; Evenepoel Kristof; De Rudder Marc; Dokter Moens Maarten (primary investigator); Prof. dr. Cattrysse Eric; Prof. Dr. D'Haens Jean Device: Trabecular Spondylolisthesis; Metal Intervertebral Degeneration of Cage with Roentgen Lumbar Stereophotogrammet Intervertebral Disc; ric Analysis beads Spinal Stenosis Device: X-STOP®; Lumbar Spinal Procedure: Stenosis Laminectomy 47 Jul-07 Dec-11 Capital District http://ClinicalTrials.gov/show/NCT00493558 Health Authority, Canada; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01185665 GO-LIF With Percutaneous Facet Fusion Single group assignment NCT01269398 Pilot Study to Evaluate Feasibility of DensiProbe Spine Assessing Bone Strength in Spinal Surgery Prospective, case-only study NCT01126385 Device: GO-LIF and Lumbar Fusion SpineAssist SYSTEMS Safety and Efficacy Study Comparing ProDisc-C to ACDF Surgery to Treat SCDD RCT, safety/efficacy study NCT00291018 Study of Epidural Steroid Injection (ESI) Versus Minimally Invasive Lumbar Decompression (MILD®) in Patients With Symptomatic Lumbar Central Canal Stenosis Phase IV: RCT, safety/efficacy study NCT00995371 Outcome Study of Patients Treated With Translational Cervical Plate Used to Treat Degenerative Disc Disease Non-randomized, parallel assignment NCT00443547 TissueLink Study During MultiLevel Spine Surgery Phase IV: RCT, efficacy study NCT01300559 Clinical Outcomes of Lumbar Degenerative Disc Disease in Active-Duty U.S. Service Personnel Single group assignment NCT01028300 Device: Total Disc Replacement Device: MILD® (Minimally Invasive Lumbar Decompression); Drug: Epidural Steroid Injection Device: DensiProbe Spinal Diseases Spine Not yet N/K Rec Adt Sen N/K Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT01269398 Adt Aug-10 Jul-11 AO Clinical http://ClinicalTrials.gov/show/NCT01126385 Sen Investigation and Documentation; University Hospital Inselspital, Berne Adt N/K Jul-11 Synthes USA http://ClinicalTrials.gov/show/NCT00291018 HQ, Inc. Rec 30 Diskectomy; Spinal Fusion; Prostheses and Implants Active, NR 228 Lumbar Spinal Stenosis Active, NR 40 Adt Aug-09 Jun-11 Coastal http://ClinicalTrials.gov/show/NCT00995371 Sen Orthopedics & Sports Medicine; Vertos Medical, Inc. Device: Anterior Degenerative Disc Cervical Discectomy Disease and Fusion (ACDF) Comp 231 Adt Mar-06 Apr-11 Synthes USA Sen HQ, Inc. Device: Tissuelink device Active, NR 60 Adt Apr-06 Apr-11 Duke University; http://ClinicalTrials.gov/show/NCT01300559 Sen Salient Surgical Technologies Term 4 Adt Low Back Pain Device: ProDisc™-L Degenerative Disc Total Disc Disease Replacement (TDR) 48 Apr-10 Mar-11 Synthes USA HQ, Inc. http://ClinicalTrials.gov/show/NCT00443547 http://ClinicalTrials.gov/show/NCT01028300 Lumbar Degenerative Disc Disease Treated With Anterior Tension Band System (ATB) With ALIF/FRA Spacer Single group assignment NCT01323387 Surgical Outcomes Using Variable Rod Diameters in the Treatment of Idiopathic Scoliosis Phase IV: RCT, safety/efficacy study NCT00510575 Device to Reduce Surgery Site Contamination - Spine RCT, safety/efficacy study NCT01262105 Spine Fusion Instrumented With BMP-2 vs Uninstrumented With Infuse BMP-2 Alone RCT, safety/efficacy study NCT00405600 Assessment of Low Level Laser Therapy for Late Postoperative Pain After Lumbar Fusion Surgery RCT NCT00422045 Evaluation of the PediGuard™ for Pedicle Screw Insertion RCT NCT00549627 Dynamic Stabilization for Lumbar Spinal Stenosis With Stabilimax NZ® Dynamic Spine Stabilization System RCT, safety/efficacy study NCT00529997 Comparison of Cervical Laminectomy to Laminoplasty RCT NCT01324622 Device: Interbody Fusion Lumbar Degenerative Disc Disease Comp 150 Device: Spinal rod Scoliosis Comp 300 Child May-07 Jan-11 Shriners Adt Hospitals for Children Device: Air Barrier System Device Surgery Comp 23 Child Nov-09 Dec-10 Nimbic Systems, http://ClinicalTrials.gov/show/NCT01262105 Adt LLC Sen Device: Infuse Bone Degenerative Graft BMP-2, Large Lumbar Disc Kit Disease; Spondylolisthesis; Spinal Stenosis Device: Low Level Surgery Laser Therapy Comp 50 Adt Nov-06 Dec-10 Capital District http://ClinicalTrials.gov/show/NCT00405600 Sen Health Authority, Canada Comp 50 Adt Dec-06 Dec-10 University of http://ClinicalTrials.gov/show/NCT00422045 Sen Toledo Health Science Campus Device: Pediguard Susp 108 Child Aug-05 Dec-10 Shriners Adt Hospitals for Sen Children http://ClinicalTrials.gov/show/NCT00549627 Device: Stabilimax Lumbar Spinal NZ® Dynamic Spine Stenosis Stabilization System Term 480 Adt Feb-07 Dec-10 Applied Spine Sen Technologies http://ClinicalTrials.gov/show/NCT00529997 Device: Laminoplasty Spinal Cord (ARCH Fixation Diseases System); Procedure: laminectomy Term 24 Adt Jan-06 Nov-10 Synthes USA Sen HQ, Inc. http://ClinicalTrials.gov/show/NCT01324622 Posterior Spinal Fusion 49 Adt Apr-04 Feb-11 Synthes USA Sen HQ, Inc. http://ClinicalTrials.gov/show/NCT01323387 http://ClinicalTrials.gov/show/NCT00510575 MAVERICK™ Total Disc Replacement- Pivotal Study Phase III: RCT, safety/efficacy study NCT00635843 Device: Spinal Diseases MAVERICK™ Disc; Device: LT-CAGE® Lumbar Tapered Fusion Device and INFUSE® Bone Graft Device: rhBMPDegenerative Disc 2/CRM/CD Disease HORIZON® Spinal System rhBMP-2/CRM/CD HORIZON® Spinal System Pilot Study (2Level) Single group assignment, safety/efficacy study NCT01491568 Comprehensive Cohort Study of Device: Brace Bracing for Adolescent Idiopathic Scoliosis (AIS): A Feasibility Study RCT, safety/efficacy study NCT00989495 A Post-Market Study of Transfacet Device: PERPOS™ Lumbar Spine Fixation and Fusion PLS Utilizing the PERPOS™ PLS System Single group assignment, efficacy study NCT00887835 Activ-L™ Artificial Disc Treatment Device: Activ-L of Degenerative Disc Disease in Artificial Disc; the Treatment of Degenerative Device: ProDisc Disc Disease Total Disc Phase III: RCT, safety/efficacy Replacement or study Charite Atifical Disc NCT00589797 Is Pleth Variability Index (PVI) a Device: Masimo Surrogate for Pulse Pressure multi-wavelength Variations (PPV) in Pediatric Spine pulse co-oximeter Fusion (SF) Surgery? Prospective, cohort study NCT00994656 Safety and Performance Study of Device: CAdisc™-L the CAdiscTM-L Lumbar Spinal (Total Disc Disc Replacement Device For CE Replacement) Marking NCT00949936 Comp 577 Adt Apr-03 Nov-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00635843 Sen and Biologics Comp 29 Adt Sen Active, NR 40 Lumbar Facet Disease Child Oct-08 Oct-10 The University of http://ClinicalTrials.gov/show/NCT00989495 Adt Hong Kong; Sen Scoliosis Research Society Not yet 100 Adt Apr-09 Oct-10 Interventional http://ClinicalTrials.gov/show/NCT00887835 Rec Sen Spine, Inc. Degenerative Disc Disease Active, NR 414 Scoliosis; Spinal Fusion Comp 24 Chronic Low Back Pain; Lumbar Degenerative Disc Disease Comp Adolescent Idiopathic Scoliosis Adt Jul-05 Nov-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01491568 and Biologics Jan-07 Jul-10 Aesculap http://ClinicalTrials.gov/show/NCT00589797 Implant Systems Child Oct-09 Jul-10 Children's http://ClinicalTrials.gov/show/NCT00994656 Adt Hospital of Philadelphia; Children's Anesthesiology Associates, Ltd. N/K Adt Oct-09 Jun-10 Ranier http://ClinicalTrials.gov/show/NCT00949936 Technology Limited 50 Percutaneous Dynamic Device: PDS Lumbar Stabilization (PDS) System Versus System; Device: Degenerative Disc Fusion for Treating Degenerative Fusion Disease Disc Disease Phase II: RCT, safety/efficacy study NCT00878579 Long-Term Outcomes for Lumbar Device: X STOP® Lumbar Spinal Spinal Stenosis Patients Treated Interspinous Process Stenosis With X STOP® Decompression Phase IV: Cohort study System NCT00534092 A-MAV™ Anterior Motion Segment Device: A-MAV™ Spinal Diseases Replacement disc Phase III: Single group assignment, safety/efficacy study NCT00635934 Phase IV Comparing Rods of Yield Device: titanium rod; Scoliosis Strengths to Correct Adolescent Device: ultra strength Idiopathic Scoliosis. stainless steel rod Phase IV: RCT, efficacy study NCT00768313 Intermittent Neurogenic Device: Aperius® Spinal Stenosis Claudication Treatment With Percutaneous APERIUS® Interspinous Spacer Phase IV: Single group assignment, safety/efficacy study NCT00887744 A Pilot Study to Evaluate an OP-1 Device: TLIF with a Degenerative Disc Putty Spinal System and an PEEK Spacer Disease Autograft Spinal System System and XIA RCT, efficacy study Spinal System NCT00678171 rhBMP-2/CRM/CD HORIZON® Device: rhBMPDegenerative Disc Spinal System Pivotal Study 2/CRM/CD Disease Phase III: RCT, safety/efficacy HORIZON® Spinal study System; Device: NCT00707265 Autograft/CD HORIZON® Spinal System Rec 292 Adt Mar-09 Jun-10 Interventional Sen Spine, Inc. Comp 69 Adt Dec-06 Jun-10 Medtronic Spine http://ClinicalTrials.gov/show/NCT00534092 Sen LLC Comp 53 Adt Dec-05 May-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00635934 Sen and Biologics Term 0 Comp http://ClinicalTrials.gov/show/NCT00878579 Child Sep-08 Apr-10 Queen's http://ClinicalTrials.gov/show/NCT00768313 Adt University; Johnson & Johnson; DePuy Orthopaedics 162 Adt Nov-06 Mar-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00887744 Sen & Biologics ECA Comp 30 Adt Feb-07 Mar-10 Olympus Biotech http://ClinicalTrials.gov/show/NCT00678171 Sen Corporation Comp 463 Adt Mar-02 Feb-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00707265 Sen and Biologics 51 Safety and Effectiveness Study of the TOPS System, a Total Posterior Arthroplasty Implant Designed to Alleviate Pain Resulting From Moderate to Severe Lumbar Stenosis Phase III: RCT, safety/efficacy study NCT00405691 Safety and Efficacy Study of Healos as a Bone Replacement to Treat Degenerative Disc Disease Phase III: RCT, safety/efficacy study NCT00316121 Dietary supplements Bone Mineral Density in Postmenopausal Women With Primary Breast Cancer Who Are Receiving Treatment on Clinical Trial CAN-NCIC-MA27 Phase III: Single group assignment NCT00354302 Drugs including biologics Dexamethasone Versus Depo Medrol in Lumbar Epidurals RCT, efficacy study NCT01397552 Device: “TOPS System” - Total Posterior Arthroplasty Implant" Comp 450 Adt Sep-06 Jan-10 Impliant, Ltd. Sen Device: HEALOS Degenerative Disc and Leopard Cage; Disease Device: Leopard Cage and Autograft Comp 138 Adt Apr-06 Jan-10 Advanced http://ClinicalTrials.gov/show/NCT00316121 Sen Technologies and Regenerative Medicine, LLC (ATRM); DePuy Spine Dietary Supplement: Breast Cancer; calcium carbonate; Osteoporosis Dietary Supplement: calcium citrate; Dietary Supplement: cholecalciferol; Drug: alendronate sodium; Drug: calcium gluconate; Drug: risedronate sodium; Other: laboratory biomarker analysis; Procedure: dual xray absorptometry Comp 497 Adt Apr-06 Mar-11 NCIC Clinical http://ClinicalTrials.gov/show/NCT00354302 Sen Trials Group; National Cancer FInstitute (NCI); only North Central Cancer Treatment Group; Southwest Oncology Group Drug: Dexamethasone; Drug: methylprednisolone acetate Invite 100 Adt Sep-09 Dec-15 State University http://ClinicalTrials.gov/show/NCT01397552 Sen of New York Upstate Medical University Low Back Pain; Leg Pain; Spondylolisthesis; Lumbar Spinal Stenosis Lumbar Spine Disc Herniation; Lumbar Radiculitis; Lumbar Back Pain 52 http://ClinicalTrials.gov/show/NCT00405691 The Effect of Prolonged Postoperative Antibiotics Administration on Rate of Infection in Patients Undergoing Posterior Spine Surgery Requiring a Hemovac Drain Phase IV: RCT, efficacy study NCT01458223 Safety and Preliminary Efficacy Study of Mesenchymal Precursor Cells (MPCs) in Subjects With Chronic Discogenic Lumbar Back Pain Phase II: RCT, safety/efficacy study NCT01290367 Drug: Antibiotic; Drug: Antibiotic Postoperative Infection Rec 600 Child Oct-11 Oct-15 The London Adt Spine Centre Sen http://ClinicalTrials.gov/show/NCT01458223 Biological: Single Dose MPCs Injection; Biological: Single Dose MPCs Injection; Procedure: Single injection of saline solution; Procedure: Single injection of hyaluronic acid Biological: teriparatide Degenerative Disc Disease Rec 100 Adt Aug-11 Jul-15 Mesoblast, Ltd. Sen http://ClinicalTrials.gov/show/NCT01290367 Lumbar Spondylosis; Lumbar Spondylolisthesis; Adult Degenerative Lumbar Scoliosis Postoperative Pain; spine, hip or knee replacement. Rec 90 http://ClinicalTrials.gov/show/NCT01292252 Rec 312 Adt Aug-11 Nov-14 University of Sen California, San Francisco; Eli Lilly and Company Adt Aug-05 Sep-14 University of Sen California, San Francisco Back Pain; Chronic Low Back Pain; Internal Disc Disruption; Degenerative Disc Disease Back Pain Rec 260 Adt Mar-10 Jun-14 Spinal http://ClinicalTrials.gov/show/NCT01011816 Sen Restoration, Inc. Susp 100 Adt Jan-12 Mar-14 University of Sen Alabama at Birmingham Use of Forteo (Teriparatide) in Posterolateral Lumbar Spine Fusion RCT, efficacy study NCT01292252 Clinical Trial of Gabapentin to Drug: Gabapentin Improve Postoperative Pain in Surgical Patients Phase III: RCT, safety/efficacy study NCT00221338 Treatment of Symptomatic Lumbar Biological: Biostat Internal Disc Disruption (IDD) With System; Drug: the Biostat® System Sodium Chloride Phase III: RCT, safety/efficacy Injection study NCT01011816 Analgesic Efficacy of Intravenous Drug: Lidocaine Lidocaine for Postoperative Pain Hydrochoride Following Adult Spine Surgery Injection, without RCT, efficacy study epinephrine; Drug: NCT01043211 Normal Saline; Drug: Normal Saline 53 http://ClinicalTrials.gov/show/NCT00221338 http://ClinicalTrials.gov/show/NCT01043211 Evaluation of the Effectiveness of Transforaminal Epidural Injections in Lumbar Disc Herniation or Radiculitis RCT, safety/efficacy study NCT01052571 A Study of Oxycodone/Naloxone Controlled-release Tablets (OXN) to Assess the Analgesic Efficacy and the Management of Opioidinduced Constipation (OIC) in Opioid-experienced Subjects With Controlled Moderate to Severe Chronic Low Back Pain Phase III: RCT, efficacy study NCT01427283 Safety and Efficacy Study of Umbilical Cord/Placenta-Derived Mesenchymal Stem Cells to Treat Ankylosing Spondylitis (AS) Phase I: RCT, safety/efficacy study NCT01420432 Analgesic Efficacy and Management of Opioid-induced Constipation (OIC) for Uncontrolled Moderate - Severe Low Back Pain Phase III: RCT, efficacy study NCT01427270 Work Productivity in Active Ankylosing Spondylitis (AS) Patients Treated With Enbrel. Phase IV: Prospective, cohort study NCT01421303 Comparison of Two Naloxone Infusion Rates on the Postoperative Recovery of Patients Undergoing Spine Fusion Surgery RCT, efficacy study NCT01531439 Drug: lumbar transforaminal epidural injections Low Back Pain Invite 120 Adt Feb-10 Jan-14 Pain Sen Management Center of Paducah Drug: Low Back Pain Oxycodone/Naloxon e controlled-release; Drug: Oxycodone HCl controlledrelease; Drug: Placebo Rec 900 Adt Aug-11 Jan-14 Purdue Pharma http://ClinicalTrials.gov/show/NCT01427283 Sen LP Biological: Human umbilical cordderived MSCs Rec 10 Adt Rec 900 Adt Aug-11 Dec-13 Purdue Pharma http://ClinicalTrials.gov/show/NCT01427270 Sen LP Active, NR 120 Adt Nov-09 Nov-13 Pfizer Sen Rec 80 Child Jun-11 Sep-13 Children's Mercy http://ClinicalTrials.gov/show/NCT01531439 Adt Hospital Kansas City Ankylosing Spondylitis Drug: Oxycodone/ Low Back Pain Naloxone controlledrelease; Drug: Oxycodone HCl controlled-release; Drug: Placebo Drug: Enbrel Ankylosing Spondylitis Drug: Naloxone; Drug: Naloxone Pain, Postoperative; Postoperative Nausea and Vomiting; Scoliosis 54 Jan-11 Dec-13 Shandong University http://ClinicalTrials.gov/show/NCT01052571 http://ClinicalTrials.gov/show/NCT01420432 http://ClinicalTrials.gov/show/NCT01421303 Comparison of Three Methods of Hemoglobin Monitoring Single group assignment NCT01284296 Phase 3 Study of Fibrocaps™ in Surgical Bleeding Phase III: RCT, efficacy study NCT01527357 Drug: Lidocaine digital block Digital Block; spinal surgery Active, NR 20 Adt Aug-10 Aug-13 University of Sen California, San Francisco Biological: Fibrocaps; Mild or Moderate Not yet 500 Adt May-12 Device: Gelatin Surgical Bleeding; Rec Sen spine, liver, vascular sponge or soft tissue surgery. Efficacy of Pregabalin in Patients Drug: Pregabalin; Lumbar Radicular Rec 38 Adt May-09 With Radicular Pain Drug: Sugar Pill Pain; Failed Back Phase IV: RCT, efficacy study Surgery Syndrome; NCT00908375 Spinal Stenosis; Herniated Disc A Multicenter, Randomized, Drug: Intradiscal Degenerative Disc Active, 30 Adt Jan-10 Double-blind, Placebo Controlled, rhGDF-5; Other: Disease NR Sen Clinical Trial to Evaluate the Water for injection Safety, Tolerability and Preliminary Effectiveness of 2 Doses of Intradiscal rhGDF-5 (Single Administration) for the Treatment of Early Stage Lumbar Disc Degeneration Phase II: RCT, safety/efficacy study NCT01124006 Anesthesia During Drug: propofol; Drug: Idiopathic Scoliosis Invite 20 Child Jan-12 Neurophysiologic Monitoring in Desflurane Adt Scoliosis Patients Sen RCT, efficacy study NCT01549873 Methadone Versus Placebo in Drug: Methadone; Postoperative Pain Invite 80 Adt May-10 Spine Fusion Drug: Saline Sen RCT, safety/efficacy study NCT01125059 Safety and Efficacy of DepoDur in Drug: DepoDur Lumbar Spine Surgery Patients RCT, safety/efficacy study NCT00335517 Lumbar Spine Surgery Active, NR 98 55 http://ClinicalTrials.gov/show/NCT01284296 May-13 ProFibrix, Inc. http://ClinicalTrials.gov/show/NCT01527357 May-13 Northwestern University http://ClinicalTrials.gov/show/NCT00908375 Apr-13 Advanced http://ClinicalTrials.gov/show/NCT01124006 Technologies and Regenerative Medicine, LLC (ATRM); DePuy Spine Jan-13 Nationwide Children's Hospital http://ClinicalTrials.gov/show/NCT01549873 Dec-12 Northwestern http://ClinicalTrials.gov/show/NCT01125059 University; Feinberg School of Medicine, Northwestern University Adt Jun-06 Nov-12 University of http://ClinicalTrials.gov/show/NCT00335517 Sen Rochester; EKR Therapeutics, Inc Study Evaluating The Use Of Drug: Etanercept Etanercept In Patients With Ankylosing Spondylitis Prospective, cohort study NCT00544557 Osteocel® Plus in Anterior Biological: Biologic Cervical Discectomy and Fusion Osteocel Plus (ACDF) Single group assignment, safety/efficacy study NCT00942045 Osteocel® Plus in eXtreme Lateral Biological: biologic, Interbody Fusion (XLIF®) Osteocel Plus Single group assignment, efficacy study NCT00948532 Osteocel® Plus in Anterior Lumbar Biological: Osteocel Interbody Fusion (ALIF) Plus Single group assignment, safety/efficacy study NCT00948831 Radiographic Analysis Using Biological: PureGen PureGen Versus Autologous Bone Osteoprogenitor Cell in Posterolateral Fusion (PLF) Allograft; Procedure: RCT Autograft bone NCT01294007 Efficacy and Safety of Drug: Oxycodone/Naloxone Controlled- Oxycodone/Naloxon release Tablets (OXN) Compared e Controlled-release; to Placebo in Opioid-experienced Drug: Placebo Subjects With Moderate to Severe Chronic Low Back Pain Phase III: RCT, safety/efficacy study NCT01358526 Impact of Tranexamic Acid on Red Drug: Tranexamic Blood Cell Transfusion in Spinal Acid; Drug: Placebo Surgery RCT, safety/efficacy study NCT01258010 Ankylosing Spondylitis Rec 1800 Adt Nov-07 Oct-12 Pfizer Sen http://ClinicalTrials.gov/show/NCT00544557 Degenerative Disc Disease in Cervical Spine Active, NR 175 Adt Feb-09 Aug-12 NuVasive Sen http://ClinicalTrials.gov/show/NCT00942045 Degenerative Disc Disease; Back Pain Active, NR 150 Adt Mar-09 Aug-12 NuVasive Sen http://ClinicalTrials.gov/show/NCT00948532 Degenerative Disc Disease, Lumbar Active, NR 70 Adt Apr-09 Aug-12 NuVasive Sen http://ClinicalTrials.gov/show/NCT00948831 Lumbar Degenerative Disc Disease Rec 50 Adt Feb-11 Aug-12 Alphatec Spine, http://ClinicalTrials.gov/show/NCT01294007 Sen Inc. Low Back Pain Rec 600 Adt May-11 Aug-12 Purdue Pharma http://ClinicalTrials.gov/show/NCT01358526 Sen LP Neurosurgery; Orthopedic Surgery; Red Blood Cell Transfusion Rec 128 Adt Apr-11 Aug-12 Centre Sen hospitalier de l'Université de Montréal (CHUM) 56 http://ClinicalTrials.gov/show/NCT01258010 Pain Relief at Iliac Crest Bone Harvest Sites in Spine Surgery Using Bupivacaine RCT, efficacy study NCT01087931 The Use of Intrathecal Morphine in the Management of Acute Pain Following Decompressive Lumbar Spinal Surgery RCT, safety/efficacy study NCT01053039 Multicenter, Randomized Placebocontrolled Clinical Trial to Evaluate the Effect of Perioperative Use of Tranexamic Acid on Transfusion Requirements and Surgical Bleeding in Major Spine Surgery Phase IV: RCT, efficacy study NCT01136590 Drug: Bupivacaine; Pain Other: Normal Saline Rec 100 Drug: Intrathecal Morphine; Drug: Intrathecal Saline Rec 150 Child Jan-10 Jul-12 University of Adt Calgary Sen Drug: Tranexamic Spinal Fusion; Acid; Drug: fisiologic Antifibrinolytic serum Agents; Hemorrhage; Blood Transfusion Rec 130 Osteocel® Plus in Posterior Lumbar Interbody Fusion (PLIF) Single group assignment, safety/efficacy study NCT00941980 Analgesic Efficacy of Repeated Doses of Intravenous (IV) Acetaminophen in Post-operative Pediatric Spine Fusion Patients Phase III: RCT, efficacy study NCT01394718 Osteocel® Plus in Transforaminal Lumbar Interbody Fusion (TLIF) Single group assignment, safety/efficacy study NCT00947583 Biological: Osteocel Degenerative Disc Plus Disease Active, NR 70 Drug: Intravenous Acetaminophen Acute Pain Following Decompressive Lumbar Spinal Surgery Pain, Postoperative Biological: Osteocel Degenerative Disc Plus Disease Rec 60 Active, NR 50 57 Adt Apr-10 Jul-12 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT01087931 http://ClinicalTrials.gov/show/NCT01053039 Adt Sep-10 Jul-12 Hospital http://ClinicalTrials.gov/show/NCT01136590 Sen Universitari Vall d'Hebron Research Institute; Hospital Vall d'Hebron; Hospital Clinic of Barcelona; Hospital Universitari de Bellvitge; Hospital de Getafe. Jun-12 Adt Jun-09 NuVasive http://ClinicalTrials.gov/show/NCT00941980 Sen Fonly Child Jul-11 Jun-12 Children's Adt Hospital of Philadelphia Adt May-09 May-12 NuVasive Sen http://ClinicalTrials.gov/show/NCT01394718 http://ClinicalTrials.gov/show/NCT00947583 Perioperative Pain Management In Drug: 150% Oral Pain Spine Surgery Patients: Part I Morphine Equivalent RCT, efficacy study (OME); Other: NCT01447888 Clinical Judgment Rec 200 Effect of Ketamine Added to Drug: Ketamine; Intravenous Patient-controlled Drug: Saline Analgesia on Postoperative Pain, Nausea and Vomiting in Patients Undergoing Lumbar Spinal Surgery Phase IV: RCT, efficacy study NCT01394406 Perioperative Intravenous Drug: Lidocaine; Lidocaine or Epidural Anesthesia Other: placebo; on Outcomes in Complex Spine Other: Morphine Surgery sulfate RCT, safety/efficacy study NCT00840996 The Effect of Zoledronic Acid to Drug: zoledronic Bone Fusion and Bone Metabolism acid; Drug: sodium of Patients With Lumbar chloride Degenerative Disease After Lumbar Interbody Fusion Phase IV: RCT, efficacy study NCT01310465 The Effect of Intravenous Drug: Intravenous Lidocaine on Pain After Lumbar lidocaine injection; Spinal Fusion Drug: Intravenous Phase IV: RCT, efficacy study normal saline NCT01319682 injection Intradiscal rhGDF-5 Phase I/II Drug: Intradiscal Clinical Trial rhGDF-5 Phase I/II: Single group assignment, safety/efficacy study NCT00813813 Postoperative Nausea and Vomiting Rec 50 Spine Surgery; Intraocular Pressure Rec Image Changes of Lumbar Fusion; Bone Turnover Markers; Bone Mineral Density Low Dose Ketamine Study on Opioid Tolerance and Hyperalgesia Phase IV: RCT, efficacy study NCT01325493 Adt Sep-11 May-12 Abbott Sen Northwestern Hospital; Allina Hospitals and Clinics Adt Jan-10 May-12 Yonsei University http://ClinicalTrials.gov/show/NCT01447888 200 Adt May-08 May-12 Outcomes Sen Research Consortium http://ClinicalTrials.gov/show/NCT00840996 Rec 50 Adt Jan-11 Apr-12 Fudan University http://ClinicalTrials.gov/show/NCT01310465 Sen Postoperative Pain Not yet Rec 54 Adt Mar-11 Feb-12 Chung-Ang Sen Univerisity Hospital Degenerative Disc Disease Active, NR 48 Rec 50 Adt Jun-08 Jan-12 Advanced http://ClinicalTrials.gov/show/NCT00813813 Sen Technologies and Regenerative Medicine, LLC (ATRM); DePuy Spine Child Jan-10 Jan-12 Children's http://ClinicalTrials.gov/show/NCT01325493 Adt Research Institute Drug: Ketamine; Idiopathic Scoliosis; Drug: Normal Saline Spondylolisthesis 58 http://ClinicalTrials.gov/show/NCT01394406 http://ClinicalTrials.gov/show/NCT01319682 Pregabalin for the Treatment of Drug: Pregabalin 150 Lumbar Spinal Pain After Posterior Spinal Fusions mg; Drug: Placebo Fusions Phase IV: RCT, safety/efficacy study NCT01366196 Intraoperative Infusion of Precedex Drug: Intravenous Spinal Fusion to Reduce Length of Stay After infusion of Acquired; Spinal Lumbar Spine Fusion Dexmedetomidine or Stenosis; Lesion of Phase IV: RCT, 0.9% Saline Lumbosacral pharmacodynamics study Intervertebral Disc; NCT00808665 Spinal Diseases The Effect of Perioperative Drug: Placebo; Drug: Postoperative Pain Ketamine on Acute and Chronic Ketamine Pain After Major Back Surgery Phase II: RCT, safety/efficacy study NCT00618423 Extension Study for Long Term Drug: SAR153191 Ankylosing Evaluation of SAR153191 (REGN 88) Spondylitis (REGN88) in Patients With Ankylosing Spondylitis Phase III: Single group assignment, safety study NCT01118728 The Analgesic Effect of Combined Drug: s-ketamine & Analgesia, PatientTreatment With Intranasal Smidazolam; Drug: controlled; Spinal ketamine and Intranasal Morphine PCA Stenosis Midazolam Phase II/III: RCT, safety/efficacy study NCT01275547 A Clinical Trial to Study the Effects Drug: Eperisone Acute of a Fixed Dose Combination of hydrochloride and Musculoskeletal Diclofenac and Eperisone Diclofenac sodium; Spasm Due to Low Hydrochloride With Plain Drug: Eperisone Back Pain Eperisone Hydrochloride in hydrochloride Patients With Low Back Pain Phase III: RCT, safety/efficacy study NCT01300312 Rec 80 Adt Oct-08 Jan-12 Hospital for http://ClinicalTrials.gov/show/NCT01366196 Sen Special Surgery, New York; Pfizer Rec 60 Adt Jun-09 Dec-11 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00808665 Rec 180 Adt Oct-07 Dec-11 University Sen Hospital, Geneva http://ClinicalTrials.gov/show/NCT00618423 Term 223 Adt Jun-10 Dec-11 Sanofi-Aventis; http://ClinicalTrials.gov/show/NCT01118728 Sen Regeneron Pharmaceuticals Rec 36 Adt Jan-11 Dec-11 University http://ClinicalTrials.gov/show/NCT01275547 Sen Hospital, Basel, Switzerland Rec 240 Adt Feb-11 Nov-11 Eisai Co., Ltd. 59 http://ClinicalTrials.gov/show/NCT01300312 Radiographic and Clinical Biological: PureGen Lumbar Rec Outcomes of PureGen in Posterior Osteoprogenitor Cell Degenerative Disc Lumbar (PLIF) and Transforaminal Allograft Disease Interbody Fusion (TLIF) Prospective, cohort study NCT01293981 Intraarticular Lumbar Joint Drug: Intra-articular Low Back Pain Rec Corticosteroid Injection(s) as a corticosteroid Treatment of Chronic Low Back injection; Drug: IntraPain in a Selected Population articular saline RCT, safety/efficacy study injection NCT01382771 The Optimal Effect Site Drug: propofol Conscious Sedation Rec Concentration of Propofol for Under Spinal Conscious Sedation in Elderly Anesthesia Male Patients Undergoing Urologic Surgery Under Spinal Anesthesia With or Without Intrathecal Fentanyl RCT, efficacy study NCT01232270 Study of Whether 15 mg Dose of Drug: Ketorolac Pain; Pain, Rec Ketorolac IV is as Effective as a 30 Tromethamine; Drug: Postoperative; spinal surgery mg Dose. Ketorolac RCT, efficacy study Tromethamine NCT01230463 Memantine for Post-Operative Drug: Memantine; Pain, Post-operative; Rec THR; TKR; lumbar Pain Control Drug: Placebo spinal fusion Phase IV: RCT, safety/efficacy study NCT01041313 Study to Evaluate the Efficacy and Drug: Hydrocodone; Pain Comp Safety of Hydrocodone Bitartrate Drug: Placebo Extended-Release Tablets (CEP33237) for Relief of Moderate to Severe Pain in Patients With Osteoarthritis or Low Back Pain Who Require Opioid Treatment for an Extended Period of Time Phase III: RCT NCT01240863 150 Adt Feb-11 Oct-11 Alphatec Spine, http://ClinicalTrials.gov/show/NCT01293981 Sen Inc. 120 Adt Oct-10 Oct-11 University of Sen Florida http://ClinicalTrials.gov/show/NCT01382771 50 Adt Oct-10 Oct-11 Yonsei Sen University http://ClinicalTrials.gov/show/NCT01232270 Monly 50 Adt Sep-10 Sep-11 University of Calgary http://ClinicalTrials.gov/show/NCT01230463 120 Adt Jan-10 Sep-11 University of Sen Washington; Forest Laboratories http://ClinicalTrials.gov/show/NCT01041313 391 Adt Nov-10 Aug-11 Cephalon Sen http://ClinicalTrials.gov/show/NCT01240863 60 Clinical Trial to Assess Safety of SI-6603 in Patients With Lumbar Disc Herniation Phase II: Single group assignment, safety/efficacy study NCT01282606 The Bupivacaine Dose Sparing Effect of Intrathecal Epinephrine RCT, safety/efficacy study NCT01261078 Drug: SI-6603 Lumbar Vertebra Hernia Drug: Placebo; Drug: Spinal Anesthesia epinephrine 25; Drug: Epinephrine 50; Drug: epinephrine 100; Drug: Epi 200 Dose Ranging Study to Evaluate Drug: SAR153191 Ankylosing the Efficacy and Safety of (REGN88); Drug: Spondylitis SAR153191 (REGN88) in Patients placebo With Ankylosing Spondylitis Phase II: RCT, efficacy study NCT01061723 A Preemptive Epidural Drug: Placebo (one Postoperative Pain Ropivacaine for Postoperative of medication); Drug: Pain Relief in Degenerative Ropivacaine Lumbar Spine Surgery (epidural injection) Phase IV: RCT, efficacy study NCT01117610 The Effect of Pregabalin and Drug: Pregabalin; Pain Dexamethasone on Acute and Drug: Chronic Pain After Lumbar Spinal dexamethasone; Surgery Drug: placebo RCT, safety/efficacy study NCT01168531 Efficacy of Ropivacaine Drug: Ropivacaine Postoperative Pain Continuous Wound Instillation Versus Single Shot After Spine Fusion Surgery Phase IV: RCT, efficacy study NCT00823576 Continuous Local Infusion of Drug: Bupivacaine; Scoliosis Anesthetic at the Incisional Site for Drug: Normal Saline Scoliosis Surgery Phase IV: RCT, safety/efficacy study NCT00508066 Active, NR 18 Adt Dec-07 Aug-11 Seikagaku Sen Corporation http://ClinicalTrials.gov/show/NCT01282606 Comp 75 Adt Dec-10 Jul-11 Seoul Medical Sen Center http://ClinicalTrials.gov/show/NCT01261078 Comp 300 Adt Feb-10 Jun-11 Sanofi-Aventis; http://ClinicalTrials.gov/show/NCT01061723 Sen Regeneron Pharmaceuticals Not yet Rec 60 Adt May-10 Apr-11 Chung-Ang Univerisity Hospital http://ClinicalTrials.gov/show/NCT01117610 Comp 108 Adt Dec-09 Mar-11 Yonsei Sen University http://ClinicalTrials.gov/show/NCT01168531 Term 64 Adt Dec-08 Mar-11 Centre http://ClinicalTrials.gov/show/NCT00823576 Sen Hospitalier Universitaire de Nice Comp 60 Child May-07 Jan-11 Shriners Adt Hospitals for Children 61 http://ClinicalTrials.gov/show/NCT00508066 The Effect of Magnesium Sulfate Drug: Magnesium Scoliosis on Motor and Somatosensory Evoked Potentials in Children Undergoing Scoliosis Surgery Phase II: RCT, efficacy study; NCT01148888 Tranexamic Acid (TXA) Versus Drug: Tranexamic Scoliosis Epsilon Aminocaproic Acid (EACA) Acid; Drug: Normal Versus Placebo for Spine Surgery Saline; Drug: Epsilon Phase IV: RCT, efficacy study aminocaproic acid NCT00958581 Gabapentin for Prophylaxis Drug: Gabapentin Intrathecal Intrathecal Morphine-Induced Morphine; Spinal Pruritus Anesthesia; RCT, safety/efficacy study Orthopedic Surgery NCT01236859 Ephedrine vs Phenylephrine - ECG Drug: Phenylephrine; Spinal Anesthesia; Changes Drug: Ephedrine Pregnancy Phase IV: RCT, safety study NCT01243970 The Darbepoetin Alfa for Ischemic Drug: Darbepoetin Surgical Complications (DISC) alfa Dose Finding Trial Phase II: Single group assignment NCT00647998 IRB-HSR# 14145 R,S Methadone: Drug: methadone Analgesia and Pharmacokinetics in Adolescents Undergoing Scoliosis Correction Phase III: RCT, pharmacokinetics study NCT01205256 Local Anesthetic Infiltration to Drug: Ropivacaine / Prevent Postoperative Pain After Placebo Lumbar Surgery Phase III: RCT, safety/efficacy study NCT00825422 Rec 15 Child Apr-10 Dec-10 The Hospital for http://ClinicalTrials.gov/show/NCT01148888 Adt Sick Children Rec 390 Child Dec-08 Dec-10 New York Adt University Sen http://ClinicalTrials.gov/show/NCT00958581 Comp 180 Child Sep-09 Nov-10 Prince of Adt Songkla Sen University http://ClinicalTrials.gov/show/NCT01236859 Nov-10 University http://ClinicalTrials.gov/show/NCT01243970 College London Hospitals; Obstetric FAnaesthetists' only Association Adt Jan-08 Oct-10 University of http://ClinicalTrials.gov/show/NCT00647998 Sen Pennsylvania Not yet 220 Child Rec Adt Sen N/K Spinal Ischemia; Stroke; Neuroprotection Susp 40 Scoliosis Invite 11 Child Mar-09 Sep-10 University of Adt Virginia http://ClinicalTrials.gov/show/NCT01205256 Hyperalgesia Comp 50 Adt Jan-09 Aug-10 University Sen Hospital, Bordeaux http://ClinicalTrials.gov/show/NCT00825422 62 SI-6603 Versus Placebo in Patients With Lumbar Disc Herniation Phase II/III: RCT, safety/efficacy study NCT00634946 Immunogenicity and Safety Study of rThrombin in Surgical Hemostasis Phase IV: Single group assignment, safety study NCT00813904 Analgetic and Anxiolytic Effect of Preoperative Pregabalin Phase IV: RCT, efficacy study NCT00353704 Influence of Dexmedetomidine on the Evoked Potentials During Spine Surgery RCT, safety/efficacy study NCT00494832 Anesthesia Induction in Patients Undergoing Surgery for Cervical Myelopathy Phase IV: RCT, safety/efficacy study NCT01052337 Post-operative Epidural Analgesia After Minimally Invasive Lumbar Decompression and Fusion RCT NCT00644111 Drug: SI-6603; Drug: Lumbar Vertebra Placebo Hernia Comp 195 Adt Jan-08 Aug-10 Seikagaku Sen Corporation http://ClinicalTrials.gov/show/NCT00634946 Biological: rThrombin, 1000 IU/mL Blood Loss, Surgical; spine, arteriovenous graft formation, or peripheral artery bypass surgical procedure Drug: pregabalin; Intervertebral Disk Drug: Placebo; Drug: Displacement; Disk morphine Prolapse Comp 31 Adt Jan-09 Jul-10 ZymoGenetics Sen http://ClinicalTrials.gov/show/NCT00813904 Comp 50 Adt Nov-05 Jun-10 Asker & Baerum http://ClinicalTrials.gov/show/NCT00353704 Sen Hospital Drug: Spine Surgery Dexmedetomidine; Drug: Normal Saline Active, NR 40 Adt Feb-08 May-10 University of Sen Washington; Hospira, Inc. http://ClinicalTrials.gov/show/NCT00494832 Drug: anaesthetics: Spinal Cord sevofluorane Diseases Rec 116 Adt Apr-09 Mar-10 University of Sen Roma La Sapienza http://ClinicalTrials.gov/show/NCT01052337 Drug: Bupivicaine, Low Back Pain Hydromorphone; Drug: Saline Placebo Rec 32 Adt Feb-08 Mar-10 University Health http://ClinicalTrials.gov/show/NCT00644111 Sen Network, Toronto 63 Effectiveness of Caudal Epidural Injections in Treatment of Chronic Low Back and Lower Extremity Pain RCT, safety/efficacy study NCT00370799 Efficacy of Gabapentin or Amitriptyline to Reduce Postoperative Pain After Lumbar Laminectomy and Diskectomy Phase II: RCT, efficacy study NCT01014520 The Effects of Potassium Citrate on Bone Metabolism Phase IV: RCT, efficacy study NCT00357331 Procedure 'Acupuncture Therapy' for Pain and Function Recovery in Spine Surgery Patients RCT, safety/efficacy study NCT01304979 Lumbar Disc Herniation Outcome Measures Prospective, case control study NCT01041391 Magnetic Resonance Imaging (MRI) Interpretations for Lumbar Spinal Stenosis (LSS) Prospective, cohort study NCT01017692 Drug: Caudal epidural injection; Drug: Caudal Epidural Injection with generic Celestone; Drug: Caudal Epidural Injection with Celestone; Drug: Caudal Epidural Injection with DepoMedrol Drug: Gabapentin , Amitriptyline Low Back Pain Active, NR 240 Adt Jan-06 Mar-10 Pain Sen Management Center of Paducah Drug: potassium citrate Herniated Disc; Intervertebral Disc Displacement Rec 120 Adt May-09 Mar-10 Tabriz University http://ClinicalTrials.gov/show/NCT01014520 Bone Diseases, Metabolic; Osteoporosis, Postmenopausal Rec 75 Adt Sen Procedure: Acupuncture therapies; Procedure: Control Pain; Low Back 'Spine Fusion' Surgery Invite 114 Adt Sep-10 Nov-00 Beth Israel Sen Medical Center Procedure: Discectomy-lumbar spine Lumbar Intervertebral Disc Herniation Invite 200 Procedure: MRI Lumbar Spinal Stenosis Invite 100 Adt May-09 Dec-20 State University http://ClinicalTrials.gov/show/NCT01041391 Sen of New York Upstate Medical University Adt Jun-09 Dec-20 State University http://ClinicalTrials.gov/show/NCT01017692 Sen of New York Upstate Medical University Fonly 64 Jul-06 Dec-09 Weill Medical College of Cornell University http://ClinicalTrials.gov/show/NCT00370799 http://ClinicalTrials.gov/show/NCT00357331 http://ClinicalTrials.gov/show/NCT01304979 Neurogenic Intermittent Claudication Evaluation Study Phase IV: RCT, efficacy study NCT00905359 Procedure: Aperius™ PercLID™ System and Standalone Decompressive Surgery Conservative Versus Aggressive Procedure: Discectomy for Primary Disc conservative Herniation With Radiculopathy discectomy; Phase IV: RCT, efficacy study Procedure: NCT01204008 aggressive discectomy A Multicenter Prospective Study of Procedure: Surgical Quality of Life in Adult Scoliosis intervention; Other: RCT, safety/efficacy study Non operative NCT00854828 intervention Surgery Versus Standardized Non- Procedure: Lumbar operative Care for the Treatment Microdiscectomy; of Lumbar Disc Herniations: A Other: Canadian Trial Physiotherapy, Phase III: RCT Epidural injections, NCT01335646 Education, Pain Medications, Antiinflammatories Spinal Stenosis Rec 280 Adt Jan-10 Dec-15 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00905359 Sen & Biologics ECA Herniated Disc Rec 100 Adt Sep-09 Dec-15 Sun Yat-sen University http://ClinicalTrials.gov/show/NCT01204008 Scoliosis Rec 300 Adt Jan-10 Dec-15 Washington Sen University (US) http://ClinicalTrials.gov/show/NCT00854828 Lumbar Spine Disc Herniation; Lumbar Radiculopathy Rec 140 Endoscopic discectomy versus microdiscectomy RCT ISRCTN11556571 An Evaluation of Interlaminar Lumbar Instrumented (ILIF™) Single group assignment, safety/efficacy study NCT01019057 Spondylolisthesis Treated With an iO-Flex® System Enabled Decompression Single group assignment, efficacy study NCT01338766 Microdiscectomy; Endoscopic discectomy Single level disease, Active L3/4, L4/5, L5/S1 140 Adt Feb-10 Mar-15 The London http://ClinicalTrials.gov/show/NCT01335646 Spine Centre; The Physicians' Services Incorporated Foundation; Lawson Health Research Institute Adt May-06 Jan-15 Joimax GmbH http://www.controlled(Germany) trials.com/ISRCTN11556571 Procedure: ILIF Degenerative Disc Disease Active, NR 100 Adt Nov-09 Dec-14 NuVasive Sen http://ClinicalTrials.gov/show/NCT01019057 Procedure: Decompression using the iO-Flex™ system Radiculopathy; Spondylolisthesis; Lumbar Spinal Stenosis Invite 150 Adt Apr-11 Nov-14 Baxano, Inc. Sen http://ClinicalTrials.gov/show/NCT01338766 65 Safety and Preliminary Efficacy Study of NeoFuse in Subjects Requiring Lumbar Interbody Fusion Phase II: RCT, safety/efficacy study NCT00996073 Procedure: Lumbar Degenerative Disc Active, 24 Interbody Fusion with Disease; NR Autograft; Procedure: Degenerative Lumbar Interbody Spondylolisthesis; Fusion with Spinal Stenosis NeoFuse; Procedure: Lumbar Interbody Fusion with NeoFuse Greenwich Lumbar Stenosis SLIP Procedure: Lumbar Spinal Stenosis; Active, 64 Study Laminectomy with Spondylolisthesis NR Phase III: RCT, efficacy study Instrumented Pedicle NCT00109213 Screw Fusion; Procedure: Lumbar Laminectomy PEEK and Allograft Spacers Procedure: Degenerative Disc Rec 240 Evaluation in Spinal Fusion Posterior/Transforam Disease Surgeries inal Lumbar Prospective, case control study Interbody Fusion NCT01406405 (P/TLIF), Anterior Cervical Discectomy and Fusion (ACDF) Efficacy and Safety Study of Procedure: The Degenerative Rec 82 Lumbar Interbody Fusion With Transforaminal Osteoarthritis; MatriTMBONE Associated With Lumbar Interbody Degenerative Autologous Bone Marrow Fusion (TLIF) Lumbar Vertebra Phase II: Single group surgery assignment, efficacy study NCT01335243 Minimally Invasive Surgery in Procedure: Adult Spinal Cord Not yet 30 Treating Patients With Spinal therapeutic Neoplasm; Rec Tumors conventional surgery; Childhood Spinal RCT, efficacy study Procedure: Cord Neoplasm; NCT01308489 therapeutic Recurrent Adult conventional surgery; Spinal Cord Procedure: quality- Neoplasm; of-life assessment Recurrent Childhood Spinal Cord Neoplasm; Spinal Bone Metastases; Spinal Cord Metastases 66 Adt Sep-09 Jul-14 Mesoblast, Ltd. Sen http://ClinicalTrials.gov/show/NCT00996073 Adt May-02 Jul-14 Greenwich Sen Hospital http://ClinicalTrials.gov/show/NCT00109213 Adt Sen Jul-11 Jul-14 Justin Parker http://ClinicalTrials.gov/show/NCT01406405 Neurological Institute; Boulder Neurosurgical Associates Adt May-11 May-14 University Hospital, Bordeaux; Biom'up http://ClinicalTrials.gov/show/NCT01335243 Adt Dec-11 Mar-14 City of Hope http://ClinicalTrials.gov/show/NCT01308489 Sen Medical Center; National Cancer Institute (NCI) Value of Functional Anesthetic and Procedure: Discogenic Pain; Provocative Discography in the Functional anesthetic Low Back Pain Surgical Treatment of Discogenic discography; Pain Procedure: Phase IV: RCT, efficacy study Provocative NCT01077947 Discography A Randomized, Equivalence Trial Procedure: Caudal Low Back Pain of Percutaneous Lumbar Epidural Injection; Adhesiolysis and Caudal Epidural Procedure: Steroid Injections percutaneous RCT, safety/efficacy study adhesiolysis NCT01053273 The Effect of Ozone Therapy for Procedure: Lumbar Herniated Lumbar Herniated Disc Discectomy/ micro Disc Phase II: RCT, efficacy study discectomy; Drug: NCT00566007 Ozone therapy; Drug: Oxygen therapy Surgical Treatment for Procedure: Surgical Scoliosis; Degenerative Scoliosis correction of the Kyphoscoliosis Prospective, cohort study deformity NCT01439906 Management of Myelomeningocele Procedure: Prenatal Meningomyelocele; Study (MOMS) Myelomeningocele Spinal Dysraphism RCT, safety/efficacy study Repair Surgery; NCT00060606 Procedure: Postnatal Myelomeningocele Repair Surgery Cost Effectiveness and Clinical Procedure: Cell Low Back Pain Utility of Cell Saver Use for Two to Saver; Procedure: Unresponsive to Three Level Lumbar Fusions No Cell Saver Non-surgical Care RCT, efficacy study NCT01453309 Effectiveness of Lumbar Fusion Procedure: NanOss Degenerative Disc When NanOss Bioactive Is Used Bioactive bone void Disease; Spinal With Posterolateral Gutter Fusions filler used in Stenosis; Prospective, case-only study posterolateral gutter Spondylolisthesis NCT01452516 fusions Wdrwn 224 Adt Feb-10 Feb-14 Northwestern http://ClinicalTrials.gov/show/NCT01077947 University; Medtronic Spine LLC Invite 120 Adt Feb-10 Jan-14 Pain Sen Management Center of Paducah http://ClinicalTrials.gov/show/NCT01053273 Rec 156 Rec 60 Adt Dec-08 Jan-14 Kovacs http://ClinicalTrials.gov/show/NCT00566007 Sen Foundation; Fondo de Investigacion Sanitaria; Hospital Negrín; Hospital Son Llatzer; Servicio de Salud de las Islas Baleares Adt Jan-10 Dec-13 Istituto http://ClinicalTrials.gov/show/NCT01439906 Sen Ortopedico Rizzoli Active, NR 183 Rec 100 Adt Feb-03 Nov-13 Eunice Kennedy http://ClinicalTrials.gov/show/NCT00060606 Sen Shriver National Institute of Child FHealth and only Human Development Not yet 240 Adt Oct-11 Oct-13 Norton http://ClinicalTrials.gov/show/NCT01453309 Rec Sen Leatherman Spine Center 67 Adt Sen Jul-10 Sep-13 Pioneer Surgical http://ClinicalTrials.gov/show/NCT01452516 Technology, Inc. A Post Market Surveillance Procedure: Surgery Spinal Deformity Validation to Evaluate the Effectiveness of the Following System: Polaris Deformity Spinal System Phase IV: Prospective, caseonly study NCT01220505 Prospective Study of Cerebral Procedure: Surgical Cerebral Palsy; Palsy Scoliosis fusion Scoliosis RCT, efficacy study NCT00958542 SPONGIT: Comparison of Two Procedure: Degenerative Surgical Approaches in the Circumferential Spondylolisthesis Treatment of Degenerative arthrodesis; Spondylolysthesis Procedure: RCT, efficacy study Posterolateral fusion NCT00869882 with instrumentation Beta-Tricalcium Phosphate Bone Procedure: Adult Spinal Cord Graft in Treating Patients musculoskeletal Neoplasm; Spinal Undergoing Surgery For Metastatic complications Bone Metastases; Spine Cancer management/prevent Spinal Cord Single group assignment, ion; Procedure: bone Compression efficacy study graft; Procedure: NCT01407341 quality-of-life assessment; Other: questionnaire administration Robotic-Assisted Surgery in Procedure: Adult Spinal Cord Treating Patients With Spine therapeutic Neoplasm; Spinal Tumors conventional surgery Bone Metastases; Single group assignment, Spinal Cord efficacy study Metastases NCT01345903 Neurologic Complications in Spinal Procedure: Routinely Adult Spinal Deformity Surgery performed surgical Deformity Prospective, case-only study correction of spinal NCT01305343 deformity Rec 200 Child Sep-10 Sep-13 Biomet, Inc. Adt Sen Rec 45 Child Mar-09 Jul-13 University of http://ClinicalTrials.gov/show/NCT00958542 Adt British Columbia Rec 70 Adt Jun-09 Jun-13 University Sen Hospital, Bordeaux Rec 20 Child Jun-11 Jun-13 USC/Norris http://ClinicalTrials.gov/show/NCT01407341 Adt Comprehensive Sen Cancer Center; National Cancer Institute (NCI) Not yet Rec 10 Adt May-12 Jun-13 City of Hope http://ClinicalTrials.gov/show/NCT01345903 Sen Medical Center; National Cancer Institute (NCI) Not yet 240 Rec 68 Adt Sen Jul-11 May-13 AOSpine International; Scoliosis Research Society (SRS) http://ClinicalTrials.gov/show/NCT01220505 http://ClinicalTrials.gov/show/NCT00869882 http://ClinicalTrials.gov/show/NCT01305343 Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion RCT NCT01018771 Reorganization of Brain Functions in Patients With Cervical Myelopathy Using fMRI and MRS Prospective, case control study NCT00447343 Procedure: Actifuse Degenerative Disc ABX; Procedure: Disease INFUSE, plus Mastergraft granules Actifuse ABX Versus INFUSE in Posterolateral Instrumented Lumbar Fusion (PLIF) With Interbody Fusion RCT NCT01013389 Evaluation of Minimally Invasive Microdiscectomy Versus Conventional Open Microdiscectomy For Lumbar Herniated Disc RCT NCT00927056 Preoperative Embolization in Surgical Treatment of Spinal Metastases. RCT, efficacy study NCT01365715 Study on the Treatment of Degenerative Lumbar Spine Stenosis With a Percutaneous Interspinous Implant Phase IV: RCT, efficacy study NCT01057641 Procedure: Actifuse Degenerative Disc ABX; Procedure: Disease INFUSE, plus master granules (MGG) Procedure: Spinal Cord Decompressive Diseases cervical spine surgery; Procedure: fMRI and MRS scan Active, NR 100 Adt Sen Jul-09 Dec-12 Apatech, Inc. http://ClinicalTrials.gov/show/NCT01018771 Rec 35 http://ClinicalTrials.gov/show/NCT00447343 Active, NR 100 Adt Sep-08 Aug-12 Lawson Health Sen Research Institute; The Physicians' Services Incorporated Foundation; American Association of Neurological Surgeons Adt Jun-07 Jul-12 Apatech, Inc. Sen http://ClinicalTrials.gov/show/NCT01013389 Procedure: Microdiscectomy Lumbar Herniated Disc Invite 50 Adt Jun-09 Jun-12 University of Sen Manitoba http://ClinicalTrials.gov/show/NCT00927056 Procedure: Preoperative embolization; Procedure: Control group Procedure: Spacer implantation; Procedure: physiotherapy Spinal Metastases Rec 64 Adt May-11 Jun-12 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01365715 Lumbar Spinal Stenosis Rec 22 Adt Mar-11 Jun-12 University of Sen Cologne http://ClinicalTrials.gov/show/NCT01057641 69 Accuracy of Lumbar Pedicle Screw Procedure: Electric Spine Pedicle Screw Placement Assisted With pulse train Placement Continuous Pulse-train Stimulation stimulation Single group assignment, safety/efficacy study NCT01342588 Evaluating the Accuracy of Procedure: Pedicle Screw of Navigation Assisted Pedicle Screw navigation assisted Fixation Placement of Spine Surgery spine surgery; RCT, safety/efficacy study Procedure: traditional NCT01247948 spine surgery Treatment of Lumbar Spinal Procedure: Minimal Lumbar Spinal Stenosis; Comparison of Two invasive Stenosis; Different Surgical Methods; Mini- decompression; Radiculopathy; invasive Decompression to X-stop Procedure: Decompression, RCT, efficacy study Interspinous Process Surgical NCT00546949 Decompression (IPD) Gait and Postural Stability Procedure: posterior Scoliosis Assessment in Children With spine fusion Idiopathic Scoliosis Undergoing Posterior Spine Instrumentation Prospective, cohort study NCT01109082 SOLAS® Spinal Surgery Registry Procedure: Surgery Vertebra; Prospective, cohort study Degeneration; Spinal NCT01372592 Trauma; Spinal Deformity Safety and Efficacy Study of Procedure: PLF with Degenerative Disc NeoFuse in Subjects Requiring autograft; Genetic: Disease; Posterolateral Lumbar Fusion PLF with NeoFuse; Degenerative Phase I/II: RCT, safety study Genetic: PLF with Spondylolisthesis; NCT00810212 NeoFuse; Genetic: Spinal Stenosis PLF with NeoFuse Real-time Ultrasound-guided Procedure: Real-time Ultrasound Spinal Spinal Anesthesia:A Feasibility ultrasound guided Anesthesia Study spinal anesthesia Prospective, cohort study NCT01326988 Rec 60 Adt Jan-11 May-12 American British http://ClinicalTrials.gov/show/NCT01342588 Sen Cowdray Medical Center Not yet 656 Rec Adt Feb-11 Feb-12 Beijing Jishuitan http://ClinicalTrials.gov/show/NCT01247948 Sen Hospital Rec 180 Adt Mar-07 Dec-11 Norwegian Sen University of Science and Technology Rec 33 Child Dec-07 Dec-11 Shriners http://ClinicalTrials.gov/show/NCT01109082 Adt Hospitals for Children; Hainer Foundation; DePuy Spine Invite 10000 Child Mar-11 Dec-11 NuVasive Adt Sen http://ClinicalTrials.gov/show/NCT00546949 http://ClinicalTrials.gov/show/NCT01372592 Active, NR 24 Adt Nov-08 Nov-11 Mesoblast, Ltd. Sen Comp 100 Adt Apr-11 Oct-11 Sunnybrook http://ClinicalTrials.gov/show/NCT01326988 Sen Health Sciences Centre 70 http://ClinicalTrials.gov/show/NCT00810212 A Clinical Study of the GO-LIF® Approach for Lumbar Spinal Fixation Single group assignment, safety/efficacy study NCT00810433 Vertos Mild - Post Market Patient Outcomes Single group assignment, safety/efficacy study NCT01076244 Percutaneous Diskectomy SpineJet x Open Microdiskectomy in Treatment of Lumbar Radiculopathy Phase IV: RCT, safety/efficacy study NCT01367860 Evaluation of Radiographic and Patient Outcomes Following Lumbar Spine Fusion Using Demineralized Bone Matrix (DBM) Mixed With Autograft RCT, safety/efficacy study NCT00254852 Robotic Assisted Vertebral Body Augmentation - a Radiation Reduction Tool Prospective, cohort study NCT01269359 Fusion Assessment Clinical Trial Prospective, cohort study NCT00736398 Procedure: GO-LIF - Lower Back Pain Guided Oblique Lumbar Interbody Fusion Rec 40 Adt Feb-09 Aug-11 Mazor Surgical Sen Technologies, Ltd. Procedure: Minimally Lumbar Spinal Invasive Lumbar Stenosis Decompression Active, NR 50 Adt Feb-10 Aug-11 The Center for http://ClinicalTrials.gov/show/NCT01076244 Sen Pain Relief, Inc.; Vertos Medical, Inc. Procedure: Open Radiculopathy; microdiscectomy; Herniated Disk Procedure: Percutaneous Diskectomy SpineJet Rec 60 Adt Jan-11 Aug-11 University of Sao http://ClinicalTrials.gov/show/NCT01367860 Sen Paulo Active, NR 94 Adt Oct-05 Aug-11 Exactech Sen Procedure: Posterior Stenosis; Lateral Fusion (PLF); Spondylolisthesis; Procedure: Anterior Degenerative Disc Lumbar Interbody Disease Fusion (ALIF); Procedure: Transforaminal lumbar interbody fusion (TLIF); Procedure: Posterior lumbar interbody fusion (PLIF); Procedure: Extreme lateral interbody fusion (XLIF) Procedure: robotic Vertebral Body assisted surgery Augmentation Procedure: Spinal fusion Degenerative Disc Disease Not yet 100 Rec Rec 50 71 Adt Sen N/K Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00810433 http://ClinicalTrials.gov/show/NCT00254852 http://ClinicalTrials.gov/show/NCT01269359 Adt Aug-08 Jun-11 Flexuspine, Inc. http://ClinicalTrials.gov/show/NCT00736398 Sen Cost effectiveness and quality of X-STOP® Neurogenic life after treatment of lumbar spinal interspinous intermittent stenosis with the X-STOP® distractor; Lumbar claudication Interspinous Process Distraction laminectomy secondary to lumbar (IPD) device or laminectomy: a spinal stenosis prospective randomised trial RCT ISRCTN88702314 Incidence of Proximal Junctional Procedure: Scoliosis; Kyphosis Kyphosis (PJK) in Long Posterior Traditional Spinal Fusion: A Study Comparing technique; Traditional Open Surgery to Procedure: Minimally Minimally Invasive Percutaneous invasive technique Technique at the Proximal Fusion Levels RCT, efficacy study NCT00890227 Effectiveness of Percutaneous Procedure: Chronic Low Back Lumbar Epidural Adhesiolysis and Percutaneous Pain Neurolysis on Low Back Pain adhesiolysis with RCT, safety/efficacy study hypertonic saline NCT00370994 neurolysis; Device: RK needle and Racz catheter system; Drug: local anesthetic, steroid, 10% sodium chloride solution Dynamic Stabilization Versus Procedure: standard; Degeneration of Fusion Procedure: new Lumbar RCT, safety/efficacy study Intervertebral Disc NCT01365754 Pilot study on the effect of Intradiscal Pulsed Discogenic low back Intradiscal Pulsed RadioFrequency RadioFrequency pain treatment for the management of treatment low back pain and ischialgia of discogenic origin Observational study ISRCTN46778702 Comp 110 Adt Jun-08 Jun-11 University http://www.controlledSen College London trials.com/ISRCTN88702314 Hospitals NHS Foundation Trust (UK) Not yet Rec 68 Adt Jun-09 May-11 Johns Hopkins Sen University http://ClinicalTrials.gov/show/NCT00890227 Active, NR 320 Adt Jan-06 Apr-11 Pain Sen Management Center of Paducah http://ClinicalTrials.gov/show/NCT00370994 Rec 440 Adt Sep-11 Apr-11 Technische Sen Universität München http://ClinicalTrials.gov/show/NCT01365754 Comp 50 Adt Mar-08 Feb-11 Orbis Medical Sen Centre SittardGeleen (Netherlands) http://www.controlledtrials.com/ISRCTN46778702 72 Evaluation of the Prosthetic Disc Replacement RCT, efficacy study NCT00640029 Procedure: Arthrodesis; Device: Arthroplasty (PRODISC-C® , PRODISC-L®, MobiC®, Mobidisc®, PrestigeLP®, AMav®, O-Mav®, DISCOCERV®) Efficacy and Safety Study of Non- Procedure: non percutaneous Vertebroplasty With percutaneous Macroporous Calcium Phosphate vertebroplasty Cement (MCPC) Phase II: Single group assignment, efficacy study NCT00931333 The Effect of Pressure Controlled Procedure: volume Ventilation on the Pulmonary control; Procedure: Mechanics in Prone Position Using pressure control the Wilson Frame: A Comparison With Volume Controlled Ventilation RCT, efficacy study NCT01272700 The Effect of Epiduroscopy and Procedure: Ozone Therapy in Patients With Epiduroscopy with Failed Back Surgery Syndrome oxygen therapy; Phase I: RCT, safety/efficacy Procedure: study Epiduroscopy with NCT01172457 ozone therapy Study of the Safety and Procedure: SingleEffectiveness of DIAM™ Spinal Level Posterior Stabilization System vs. Decompression; Decompression, Formerly vs. Device: DIAM Spinal Posterolateral Fusion Stabilization Phase III: RCT, safety/efficacy study NCT00627497 Lumbar Degenerative Disc Disease; Cervical Degenerative Disc Disease; Kyphosis Term 301 Adt Feb-08 Feb-11 Assistance Publique Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT00640029 Vertebra Trauma Comp 4 Adt Jul-09 Feb-11 University Hospital, Bordeaux http://ClinicalTrials.gov/show/NCT00931333 Herniation of Lumbar Comp Vertebral Disc 40 Adt Aug-10 Jan-11 Yonsei University http://ClinicalTrials.gov/show/NCT01272700 Low Back Pain; Failed Back Surgery Syndrome Rec 30 Adt May-09 Dec-10 University of Sao http://ClinicalTrials.gov/show/NCT01172457 Sen Paulo Degenerative Lumbar Spinal Stenosis Term 26 Adt Feb-08 Dec-10 Medtronic Spinal http://ClinicalTrials.gov/show/NCT00627497 Sen and Biologics 73 Intravenous Fentanyl or Local Anesthetic Infiltration for Pain Reducing During Spinal Needle Insertion NCT01157247 Ultrasound-assisted Spinal Anaesthesia in Patients With Difficult Anatomical Landmarks RCT, efficacy study NCT00956137 VERTOS-II. Percutaneous Vertebroplasty Versus Conservative Therapy RCT, safety/efficacy study NCT00232466 Procedure: Anesthesia; Spinal Comparison of Puncture intravenous fentanyl and local anesthetic infiltration in pain reducing during spinal needle puncture Procedure: Spinal Anesthesia Ultrasound guidance; Procedure: Manual palpation Comp 88 Adt Rec 180 Adt May-09 Jun-10 University Health http://ClinicalTrials.gov/show/NCT00956137 Sen Network, Toronto Procedure: Vertebroplasty Osteoporosis; Back Pain Active, NR 200 Vertebral metastases of Multiple Myeloma Comp 104 Adt Oct-05 May-10 UMC Utrecht; http://ClinicalTrials.gov/show/NCT00232466 Sen ZonMw: The Netherlands Organisation for Health Research and Development Adt Jun-07 Mar-10 Erasmus http://www.controlledSen Medical Centre trials.com/ISRCTN48083859 (The Netherlands) Patients With Paraspinal or Paraspinal Metastases Rec 90 Adt Jun-11 Sep-16 University Health http://ClinicalTrials.gov/show/NCT01290562 Sen Network, Toronto Spinal Metastases; Vertebral Metastases; Benign Spinal Tumors; Chordoma; Meningioma; Schwannoma; Neurofibroma; Paragangliomas; Arteriovenous Malformations Rec 50 Adt Sep-08 Sep-15 St. John's Mercy http://ClinicalTrials.gov/show/NCT01347307 Sen Research Institute, St. Louis VErtebroplasty versus Vertebroplasty; Radiotherapy As palliative Radiotherapy treatment of vertebral metastases of Multiple Myeloma (M. Kahler) Other Stereotactic Body Radiotherapy (SBRT) for Spinal/Para-Spinal Metastases (Spine SBRT) Phase II: Single group assignment, efficacy study NCT01290562 Radiation: Stereotactic Body Radiotherapy (SBRT); Radiation: Stereotactic Body Radiotherapy (SBRT) Stereotactic Body Radiotherapy for Radiation: Spine Tumors stereotactic body Phase IV: Single group radiotherapy; assignment, safety/efficacy Radiation: study stereotactic body NCT01347307 radiotherapy 74 Apr-09 Jul-10 Croatian Society http://ClinicalTrials.gov/show/NCT01157247 of Regional Anesthesia and Analgesia Image-Guided Radiosurgery or Stereotactic Body Radiation Therapy in Treating Patients With Localized Spine Metastasis Phase II/III: RCT NCT00922974 Intervertebral Disc Augmentation With Minimally Invasive Surgical Procedure Prospective, case-only study NCT01442922 Isometric Muscle Training in Patients With Spinal Bony Metastases Under Radiation Therapy Phase II: RCT, safety/efficacy study NCT01409720 High Dose Intensity Modulated Proton Radiation Treatment +/Surgical Resection of Sarcomas of the Spine, Sacrum and Base of Skull Phase II: Single group assignment, safety/efficacy study NCT01346124 Epidural Steroid Injection Versus Epidural Steroid Injection and Manual Physical Therapy and Exercise in the Management of Lumbar Spinal Stenosis RCT NCT00786981 Radiation: external beam radiation therapy; Radiation: image-guided radiation therapy; Radiation: radiosurgery; Radiation: stereotactic body radiation therapy Other: completion of the (VAS) for level of back pain; Other: completion of the (OLBPQ) for assessment of function Other: exercise Metastatic Cancer; Pain Rec 283 Adt Nov-09 Jul-15 Radiation http://ClinicalTrials.gov/show/NCT00922974 Sen Therapy Oncology Group; National Cancer Institute (NCI) Degenerative Disc Disease Rec 25 Adt Mar-11 Mar-15 University of Florida Not yet Rec 60 Adt Sep-11 Sep-14 University of http://ClinicalTrials.gov/show/NCT01409720 Sen Heidelberg; Dept of Radiation Oncology, University of Heidelberg, Germany Adt Jul-11 Sep-14 Massachusetts http://ClinicalTrials.gov/show/NCT01346124 Sen General Hospital; M.D. Anderson Cancer Center; National Cancer Institute (NCI) Vertebral Bony Metastases Radiation: High Dose Chordoma of Spine; Not yet 120 Intensity Modulated Chordoma of Rec Proton Radiation Sacrum; Chordoma of Base of Skull; Chondrosarcoma of the Spine; Chondrosarcoma of the Sacrum Other: Epidural Lumbar Spinal steroid injection plus Stenosis physical therapy; Other: Epidural steroid injection Rec 80 75 Adt Apr-09 May-14 Franklin Pierce Sen University; University of Colorado, Denver http://ClinicalTrials.gov/show/NCT01442922 http://ClinicalTrials.gov/show/NCT00786981 AttraX® Putty in spinal interbody fusion: Evaluation of radiographic and clinical outcomes Non-randomized, parallel assignment ISRCTN38726728 This Study is to Determine if Degenerative Spinal Pain and Disorders Cause the Levels of Substance P to Change in a Patients Saliva, Blood and/or Cerebrospinal Fluid. Prospective, case control study NCT01458938 Patient Positioning in Lumbar Fusion Surgery and Its Impact on Spinal Sagittal Balance and Surgeon Satisfaction RCT, efficacy study NCT01326091 Voice and Swallowing Outcomes Following Revision Anterior Cervical Spine Surgery Prospective, cohort study NCT01017055 Collecting Bone Graft During Spinal Decompression and Posterolateral Lumbar Fusion to Better Define Bone Making Cells Prospective, case-only study NCT01409954 Low Back Study to Compare Traditional Physical Therapy With Combined Therapy Protocol RCT, efficacy study NCT01236092 Anterior Approach Persistent back Cervical Interbody and/or leg pain Fusion; Anterior unresponsive to Approach Lumbar conservative Interbody Fusion; treatment Posterior Approach Lumbar Interbody Fusion Other: treatment plan Spinal Disease,; Spinal Radiculopathy,; Myelopathy; Neurogenic Claudication Active 150 Adt Dec-11 Dec-13 NuVasive, Inc. Sen (USA) Invite 40 Adt Other: Hyperlordotic Intervertebral Disk Positioning Degeneration Rec 52 Adt Mar-11 Mar-13 Duke University http://ClinicalTrials.gov/show/NCT01326091 Other: Voice and Swallowing evaluations Rec 50 Adt Oct-09 Mar-13 University of Sen Alabama at Birmingham http://ClinicalTrials.gov/show/NCT01017055 Genetic: Autologous Pseudarthrosis After Bone Harvest Fusion or Arthrodesis Invite 60 Adt Oct-11 Jan-13 University of Sen Utah http://ClinicalTrials.gov/show/NCT01409954 Other: conservative Radiculopathy; Low therapy - traction, Back Pain vibration, exercise Not yet Rec 36 Adt http://ClinicalTrials.gov/show/NCT01236092 Dysphagia; Dysphonia 76 http://www.controlledtrials.com/ISRCTN38726728 Jul-09 Oct-13 Carolina http://ClinicalTrials.gov/show/NCT01458938 Neurosurgery & Spine Associates Jan-11 Dec-12 Legend Healthcare Spinal Fusion and Rehabilitation Study RCT, safety/efficacy study NCT00834015 Other: Outcome of lumbar spinal fusion patients and significance of postoperative exercise therapy: RCT The Value of Traction in Treatment Other: Physical of Lumbar Radiculopathy therapy Phase III: RCT, efficacy study rehabilitation; Other: NCT00942227 Physical therapy rehabilitation Resistance Exercise Effects on Fear Avoidance and Physical Function in Obese Older Adults With Low Back Pain RCT, efficacy study NCT01250262 Spondylolisthesis, Degenerative; Spondylolisthesis, Isthmic Rec 100 Sciatica; Radiculopathy; Spinal Diseases; Musculoskeletal Diseases; Neuromuscular Diseases; Intervertebral Disk Displacement Low Back Pain; Obesity Rec 120 Other: normal Rec medical care and follow up; Other: Isolated Lumbar Resistance Exercise Program; Other: Total Body Resistance Exercise Program Effects of a Walking Program on Other: Walking Lumbar Spinal Invite Functional Status of Post-Surgical program Stenosis Lumbar Spinal Stenosis Patients RCT NCT00958490 Strategy for Maintaining Partial Other: TOF count Brain Surgery With Rec Neuromuscular Blocking Adequate guided adjustment; Motor Evoked for Motor Evoked Potential During Other: T1/ T0 guided Potential Monitoring; Neurosurgery adjustment; Other: Spine Surgery With RCT, safety study T2/ T0 guided Motor Evoked NCT01388868 adjustment Potential Monitoring Arterial Pulse Waveform Contour Other: goal directed Surgical Procedures, Rec Analysis for Intraoperative Goal therapy Operative Directed Therapy in Major Spine Surgery RCT, efficacy study NCT01124474 Adt May-10 Dec-12 Jyväskylä http://ClinicalTrials.gov/show/NCT00834015 Sen Central Hospital; Tampere University Hospital; University of Tampere Adt Jul-09 Dec-12 Intermountain http://ClinicalTrials.gov/show/NCT00942227 Health Care, Inc.; University of Utah; Wilford Hall Medical Center; Empi, A DJO Company 60 Adt Nov-10 Nov-12 University of Sen Florida http://ClinicalTrials.gov/show/NCT01250262 50 Adt Jun-09 Jun-12 University of Sen Manitoba http://ClinicalTrials.gov/show/NCT00958490 90 Adt Jun-11 May-12 Samsung Sen Medical Center http://ClinicalTrials.gov/show/NCT01388868 60 Adt Dec-10 Apr-12 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT01124474 77 Rehabilitation Following Lumbar Other: Rehabilitation Disc Surgery following lumbar disc RCT, efficacy study surgery (discectomy) NCT00894972 Study of 3 Doses of NeoFuse Genetic: NeoFuse; Combined With MasterGraft Procedure: Granules in Subjects Requiring posterolateral spinal Posterolateral Lumbar Fusion fusion with (PLF) instrumentation Phase I/II: RCT, safety study; NCT00549913 Do Lower Spine Injections Improve Other: Observation Outcomes for Lower Back Pain of biomechanical Patients effects post injection Prospective, case-only study NCT01381224 Intraocular Pressure During Prone Other: table tilt Spinal Surgery Phase II: Prospective study NCT00176722 Lumbar Disc Herniation; Radiculopathy Rec 70 Adt Active, NR 40 Adt Oct-07 Mar-12 Mesoblast, Ltd. Sen http://ClinicalTrials.gov/show/NCT00549913 Low Back Pain Rec 30 Adt Jan-11 Jan-12 University of Sen Florida http://ClinicalTrials.gov/show/NCT01381224 Spine Surgery; Vision Impairment Term 7 Adt Post Market Study of the Other: Physical Electrophysiological Course of Low Therapy Back Pain Using CERSR Technology Prospective, cohort study NCT01403870 Evaluation of the Brain Activity Other: fMRI and During Spinal Cord Stimulation in MRS Failed Back Surgery Syndrome Using Functional MRI and MRS Single group assignment NCT01181817 Low Back Pain Term 6 Failed Back Surgery Syndrome Rec 40 Degenerative Disc Disease; Spondylolisthesis; Spinal Stenosis 78 Apr-09 Apr-12 University of Utah http://ClinicalTrials.gov/show/NCT00894972 Jun-06 Jan-12 University of http://ClinicalTrials.gov/show/NCT00176722 Medicine and Dentistry New Jersey; Foundation for Anesthesia Education and Research; New Jersey Eye Institute Adt Apr-11 Nov-11 Verium http://ClinicalTrials.gov/show/NCT01403870 Sen Diagnostics, Inc. Adt Sep-08 Sep-11 Universitair http://ClinicalTrials.gov/show/NCT01181817 Sen Ziekenhuis Brussel; Maarten Moens Establishment of Optimal Transfusion Threshold During Spine Surgery RCT, efficacy study NCT00967109 Other: Allowed drop Anemia; Spine Comp 60 in hemoglobin to Surgery level between 4,5-5,6 mmol/L; Other: Allowed drop in hemoglobin to level between 5,6-6,5 mmol/L A Study on the Use of Educational Other: Educational Decompression, Not yet 70 Programs Prior to Lumbar Spinal program Surgical Rec Surgery RCT NCT00719485 Stereotactic Body Radiation Radiation: Metastatic Cancer; Rec 42 Therapy and Vertebroplasty in stereotactic body Pain; Unspecified Treating Patients With Localized radiation therapy Adult Solid Tumor, Spinal Metastasis Protocol Specific Phase II NCT00855803 Efficacy of Surgical Preparations in Other: DuraPrep; Infection Comp 100 Lumbar Spine Surgery Other: ChloraPrep RCT, efficacy study NCT01105195 Study Evaluating the Safety of Other: There is no Ankylosing Term 880 Etanercept in Rheumatoid Arthritis, Intervention. The Spondylitis; Arthritis, Ankylosing Spondylitis and study is Psoriatic; Arthritis, Psoriatic Arthritis observational. Rheumatoid; Prospective, cohort study Spondylitis, NCT00273858 Ankylosing Miscellaneous observational studies Neurological Surgery & Affiliated Services De-Identified Clinical Outcomes Database Prospective, cohort study NCT00593411 Cognitive Dysfunction in Hypertensive Patients Having Spine Surgery Prospective, case control study NCT01140854 Central Nervous System Disorder; Spinal Diseases; Peripheral Neuropathy Hypertension Rec Adt Sep-09 Feb-11 Rigshospitalet, Sen Denmark; TrygFonden, Denmark Adt Apr-09 Feb-11 Sunnybrook http://ClinicalTrials.gov/show/NCT00719485 Sen Health Sciences Centre Adt Feb-09 Feb-11 Simmons Sen Cancer Center http://ClinicalTrials.gov/show/NCT00855803 Adt Jan-10 Nov-10 Northwestern Sen University; 3M http://ClinicalTrials.gov/show/NCT01105195 Adt Mar-06 Jul-10 Wyeth is now a Sen wholly owned subsidiary of Pfizer http://ClinicalTrials.gov/show/NCT00273858 10000 Child Jun-05 Jun-15 University of Adt Sen Rec 150 79 http://ClinicalTrials.gov/show/NCT00967109 http://ClinicalTrials.gov/show/NCT00593411 California, Irvine Adt Jan-09 Dec-14 Columbia http://ClinicalTrials.gov/show/NCT01140854 Sen University; Mount Sinai School of Medicine; Weill Medical College of Cornell University XLIF® vs. MAS®TLIF for the Treatment of Symptomatic Lumbar Degenerative Spondylolisthesis With or Without Central Stenosis. Prospective, cohort study NCT01024699 CopiOs Posterolateral Fusion Procedure Prospective, cohort study NCT01123850 Direct Stimulation Of Spinal Nerve Roots To Determine Sensory And Motor Innervation Patterns Prospective, cohort study NCT00696501 Transfusion Requirements During Spinal Surgery for Severe Scoliosis Prospective, case-only study NCT01490164 Effect of HIV Infection and Highly Active Antiretroviral Treatment (HAART) on Bone Homeostasis Cross-sectional, cohort study NCT01020045 Spondylolisthesis Rec 110 Adt Nov-09 Dec-14 NuVasive Sen http://ClinicalTrials.gov/show/NCT01024699 Spondylolisthesis; Stenosis Rec 85 Adt Jun-10 Jun-14 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT01123850 Spine Surgery; Neuromuscular Mapping; Neurodiagnostics Rec 1000 Adt May-06 May-14 Lahey Clinic Sen http://ClinicalTrials.gov/show/NCT00696501 Scoliosis Rec 50 HIV Infection; Osteopenia; Osteoporosis Rec 120 Trinity Evolution in Posterior or Transforaminal Lumbar Interbody Fusion (PLIF/TLIF) Prospective, case-only study NCT00965380 Lumbar Spinal Fusion System Prospective study NCT00758719 Maverick Total Disc Replacement in a 'Real World' Patient Population Prospective, case-only study NCT01338493 Degenerative Disc Disease Active, NR 200 Degenerative Disc Disease Active, NR 53 Degenerative Disc Disease Active, NR 150 Child Feb-09 Feb-13 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01338493 Adt & Biologics ECA Sen 80 Child Aug-09 Mar-14 University of Adt Medicine and Dentistry New Jersey http://ClinicalTrials.gov/show/NCT01490164 Adt Oct-10 Jan-14 Emory http://ClinicalTrials.gov/show/NCT01020045 University; National Institute of Arthritis and Musculoskeletal and Skin Diseases Adt Sep-09 Nov-13 Orthofix Inc. http://ClinicalTrials.gov/show/NCT00965380 Sen Adt Sep-08 Jul-13 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT00758719 Analysis of Tokuhashi Score Prospective, case-only study NCT01210508 Cancer; Metastases; Spinal metastases Invite Prospective Study of Scheuermann's Kyphosis Prospective, case control study NCT00738309 Multi-Center Prospective Evaluation of Operative Versus Nonoperative Treatment for Adult Spinal Deformity Prospective, case control study NCT00738439 Center Blade Study Prospective, case control study NCT01499680 A Prospective, Multicenter Observational Study on MAST™ (Minimal Access Spinal Technologies) Fusion Procedures for the Treatment of the Degenerative Lumbar Spine Prospective, case-only study NCT01143324 Prospective Study of Minimally Invasive Spine Surgery Prospective study NCT01045473 Scheuermann's Kyphosis Invite Spinal Deformity Invite Assessment of Central Pain in Patients Who Undergo Spinal Surgery and Influence in Surgery Outcome Prospective, cohort study NCT01299818 Degeneration of Invite Lumbar Intervertebral Disc Degenerative Active, Lumbar Spine NR Causing Back and/or Leg Pain; Degenerative Lumbar Spine Pathology 167 Child Mar-09 Dec-12 State University http://ClinicalTrials.gov/show/NCT01210508 Adt of New York Sen Upstate Medical University; Cleveland Clinic Florida 240 Child May-06 Dec-12 Children's http://ClinicalTrials.gov/show/NCT00738309 Adt Specialists Foundation; DePuy Spine 936 Adt Oct-08 Dec-12 Children's http://ClinicalTrials.gov/show/NCT00738439 Sen Specialists Foundation; DePuy Spine 300 Adt Oct-11 Oct-12 NuVasive Sen 250 Adt Jun-10 Oct-12 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01143324 Sen & Biologics ECA Degenerative Disk Not yet 450 Disease; Rec Spondylolisthesis; Spinal Stenosis; Degenerative Scoliosis Spinal Surgery; Pain Not yet 50 Rec 81 http://ClinicalTrials.gov/show/NCT01499680 Adt Jan-10 Jun-12 Society for Sen Minimally Invasive Spine Surgery http://ClinicalTrials.gov/show/NCT01045473 Adt Mar-11 Apr-12 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT01299818 Stabilimax Investigational Device Exemption (IDE) Clinical Investigation Patient Followup Study Prospective, case-only study NCT01485289 NeuroVision® Dynamic Screw Test Study Prospective study NCT01232517 Antiplatelet Therapy Continuation in Spine Surgery - Its Effect on Postoperative Morbidity and Mortality Prospective, cohort study NCT01006083 Satellite™ PEEK Nucleus Replacement Retrospective Analysis Retrospective, cohort study NCT01110967 Physical Capability Outcomes After Single-Level PD-L vs SingleLevel ALIF: a Multi-Center Clinical Trial Prospective, cohort study NCT01055574 Progression of Spinal Fusion in Ankylosing Spondylitis NCT00085995 Use of ROTEM for Multi-level Spine Surgery Prospective, case-only study NCT00839995 Pilot Study on the Effect of Dexmedetomidine on Inflammatory Responses in Patients Undergoing Lumbar Spinal Fusion Prospective, cohort study NCT01377623 Spinal Stenosis Rec 25 Adt Aug-11 Mar-12 Rachiotek LLC Sen http://ClinicalTrials.gov/show/NCT01485289 Comp 60 Adt Mar-09 Feb-12 NuVasive Sen http://ClinicalTrials.gov/show/NCT01232517 Hemorrhage; Not yet 200 Cerebrovascular Rec Accident; Myocardial Infarction; Pulmonary Embolism; Deep Vein Thrombosis Degenerative Disc Active, 95 Disease, Lumbar; NR Disc Herniation, Lumbar Adt Jan-10 Feb-12 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT01006083 Physical Capability Outcomes Term 45 Adt Spondylitis, Ankylosing Rec 65 Adt Sen Coagulation Comp 41 Adt Sen Rec 56 Adt Sen Degenerative Spinal Conditions Spinal Stenosis; Inflammation 82 Adt Apr-10 Feb-12 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01110967 Sen & Biologics ECA Oct-09 Jan-12 Gundersen Lutheran Medical Foundation; Synthes USA HQ, Inc. Jun-04 Jan-12 National Institute of Arthritis and Musculoskeletal and Skin Diseases Feb-09 Dec-11 Weill Medical College of Cornell University Sep-10 Dec-11 New York University School of Medicine; Hospira, Inc. http://ClinicalTrials.gov/show/NCT01055574 http://ClinicalTrials.gov/show/NCT00085995 http://ClinicalTrials.gov/show/NCT00839995 http://ClinicalTrials.gov/show/NCT01377623 Pharmacokinetics of Aminocaproic Acid in Scoliosis Surgery Prospective, case control study NCT01408823 Scoliosis Comp 20 Radiofrequency Nerve Ablation Versus Sham to Treat Chronic Low Back Pain Caused by Sacroiliac Joint Dysfunction Prospective, case-crossover study NCT01104051 Prevalence of Inadvertent Hyperventilation During Intraoperative Anesthetic Care Retrospective, case-only study NCT01235650 Study and Surgical Treatment of Syringomyelia NCT00011245 Sacroiliac Joint Dysfunction Comp 39 Spinal Fusion Comp 160 Child Sep-10 Jul-11 Nationwide Adt Children's Sen Hospital Syringomyelia Comp 50 Evaluation of Radiculitis Following Use of Bone Morphogenetic Protein-2 for Interbody Arthrodesis in Spinal Surgery Prospective, case control study NCT00984672 A Prospective Natural History Study of Patients With Syringomyelia Prospective study NCT01150708 Establishing the Physiology of Syringomyelia NCT00001327 Lumbar Degenerative Disease Rec 240 Syringomyelia; Arnold Chiari Deformity Rec 120 Adt Jun-10 Apr-11 National Institute http://ClinicalTrials.gov/show/NCT01150708 Sen of Neurological Disorders and Stroke (NINDS) Comp 120 Adt Sen Comp 38 Posterior Lateral Fusion (PLF) With Dynesys Prospective, cohort study NCT00791180 Arnold Chiari Deformity; Hydrocephalus; Syringomyelia Spondylolisthesis 83 Child Jul-11 Oct-11 Children's http://ClinicalTrials.gov/show/NCT01408823 Adt Hospital of Philadelphia; Children's Anesthesiology Associates, Ltd. Adt Apr-10 Sep-11 Coastal http://ClinicalTrials.gov/show/NCT01104051 Sen Orthopedics & Sports Medicine http://ClinicalTrials.gov/show/NCT01235650 Adt Feb-01 May-11 National Institute http://ClinicalTrials.gov/show/NCT00011245 Sen of Neurological Disorders and Stroke (NINDS) Adt Mar-09 Apr-11 Mayo Clinic http://ClinicalTrials.gov/show/NCT00984672 Sen Jul-92 Mar-11 National Institute http://ClinicalTrials.gov/show/NCT00001327 of Neurological Disorders and Stroke (NINDS) Adt Mar-06 Mar-11 Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00791180 Sen Drug Use Survey (DUS) of Triple Therapy (Methycobal (MBL)+ Myonal (MYO)+ Non-steroidal Antiinflammatory Drags (NSAID)) on the Symptom Relief of Lumbar DDD in China Retrospective, case-only study NCT01299077 Prospective Clinical Evaluation of the New Aegis Plate for Anterior Interbody Fusions Prospective, case-only study NCT00555659 Genetic Determinants of Ankylosing Spondylitis Severity NCT00056849 Lumbar Disc Degenerative Disease Comp 478 Adt Jun-10 Nov-10 Eisai China Inc. http://ClinicalTrials.gov/show/NCT01299077 Sen Degeneration; Spondylosis; Spondylolithesis; Stenosis Active, NR 104 Adt Sep-07 Sep-10 Columbia Sen Orthopaedic Group, LLP; DePuy Spine Ankylosing Spondylitis Minimal Access Surgical Technique (MAST) in Obese Patients in Degenerative Lumbar Disease Retrospective, cohort study NCT01195584 Intraocular Pressure During Spine Surgery Prospective, cohort study NCT00593359 Degenerative Lumbar Disease 2000 Adt Mar-03 Jul-10 National Institute http://ClinicalTrials.gov/show/NCT00056849 Sen of Arthritis and Musculoskeletal and Skin Diseases Comp 72 Adt May-10 Jul-10 General Hospital http://ClinicalTrials.gov/show/NCT01195584 Sen Amstetten Intraocular Pressure Comp http://ClinicalTrials.gov/show/NCT00555659 Rec 60 84 Adt Dec-07 Feb-10 Outcomes Sen Research Consortium http://ClinicalTrials.gov/show/NCT00593359 A4. THORAX Title Phases: trial design (control) CT ID Device Sternal Closure With STERNUMFIX in Patients With High Risk Phase IV: RCT, safety/efficacy study NCT01408745 Infection Rate of Vertical Expandable Prosthetic Titanium Rib Implants (VEPTR) Prospective, cohort study NCT01085669 Interventions Flail Chest - Rib Fixation Study Phase IV: RCT, safety/efficacy study NCT01147471 Evaluation of Surgical Treatment on Pain and Disability for Chronic, Non-healing Rib Fracture Phase IV: Single group assignment, efficacy study NCT00774618 Device: operative rib Flail Chest fixation Evaluation of Primary Plating in Sternotomy Patients for Osteosynthesis and Pain Phase IV: RCT, safety/efficacy study NCT00819286 Conditions Recruit n Age Start (Grp) Date End Sponsors Date Device: Sternumfix; Sternum Wound Procedure: steel wire Infection; Nonunion of Fracture of Sternum Rec 415 Child Jun-08 Nov-12 Aesculap AG Adt Sen Device: Microbiological analysis of retained VEPTR Implants Rec 50 Infection Device: RibLoc ® Rib Rib Fracture Fracture Plating System, BioBridge™Bioresor bable Bone Fracture Plate System Other: Operative management without a device. Device: SternaLock Sternal Wound Rigid Fixation Infection; Sternal System; Device: Non-union; Pain; Wire (control) Mediastinitis Rec Active, NR Active, NR URL http://ClinicalTrials.gov/show/NCT01408745 Child Sep-09 May-12 Centre http://ClinicalTrials.gov/show/NCT01085669 Adt Hospitalier Universitaire Vaudois; University Children's Hospital Basel 100 Adt Sep-10 Mar-12 Virginia http://ClinicalTrials.gov/show/NCT01147471 Sen Commonwealth University; Synthes Inc. 50 Adt Oct-08 Dec-11 Oregon Health http://ClinicalTrials.gov/show/NCT00774618 Sen and Science University; ACUTE Innovations, LLC 141 85 Adt Dec-08 Dec-11 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT00819286 MatrixRIB Implants for Surgical Stabilization of Flail Chest Injuries: A Registry Phase IV: Prospective, cohort study NCT00810251 Pain Relief for Ventilated Patients With Multiple Rib Fractures Using the ON-Q Pain Relief System Phase IV: RCT, efficacy study NCT00880529 Improvement of Hemostasis Techniques After Median Sternotomy Phase IV: RCT, safety/efficacy study NCT01134471 Comp 20 Adt Dec-08 May-11 Legacy Sen Biomechanics Laboratory; Synthes Inc. http://ClinicalTrials.gov/show/NCT00810251 Term 48 Adt Feb-09 May-11 Cooper Sen University Hospital http://ClinicalTrials.gov/show/NCT00880529 Invite 75 Adt Apr-09 May-11 Aarhus Sen University Hospital; MCeremed, Inc. only http://ClinicalTrials.gov/show/NCT01134471 Drug: Epidural Postoperative Pain Analgesia; Drug: Patient-Controlled IV Analgesia Comp 110 Child Oct-06 Oct-10 Children's Mercy http://ClinicalTrials.gov/show/NCT00413582 Adt Hospital Kansas City Procedure Delayed Primary Versus Late Secondary Wound Closure in Sternum Infections RCT, safety/efficacy study NCT01473979 Procedure: Surgical Mediastinitis closure of the poststernotomy wound infection Not yet 100 Rec Treatment of Acute, Unstable Chest Wall Injuries RCT NCT01367951 Procedure: Surgical fixation; Procedure: conservative treatment Drugs including biologics Pain Management for Pectus Excavatum Repair RCT, efficacy study NCT00413582 Flail Chest: A Randomized Controlled Study RCT, efficacy study NCT01308697 Device: MatrixRIB (FDA Approval # K081623) Flail Chest Device: ON-Q Rib Fractures bupivicaine administration; Drug: IV opioid administration Device: Ostene; Sternal Dehiscence; Device: Bonewax Sternal Infection; Sternal Pain Blunt Injury of Thorax; Flail Chest; Chest Wall Injury Trauma; Rib Fracture Procedure: Operative Flail Chest fixation of flail chest; Other: Non Operative management Rec 80 Rec 20 86 Adt Jan-12 Jul-14 University of Sen Lausanne Hospitals; University Hospital Olomouc Child Jul-11 Dec-13 St. Michael's Adt Hospital, Sen Toronto http://ClinicalTrials.gov/show/NCT01473979 http://ClinicalTrials.gov/show/NCT01367951 Adt Apr-11 Jul-12 University of http://ClinicalTrials.gov/show/NCT01308697 Sen British Columbia Trial of Operative Fixation of Fractured Ribs in Patients With Flail Chest Phase II: RCT, safety/efficacy study NCT00298259 Procedure: operative Flail Chest; fixation of fractured Ventilation ribs Other Prediction and Characterization of Other: Conditioned Acute and Chronic Postoperative pain modulation Pain Prospective, cohort study NCT01308385 Miscellaneous observational studies VEPTR Implantation to Treat Children With Early Onset Scoliosis Without Rib Abnormalities Prospective, cohort study NCT00689533 Pain; Pain, Postoperative; Funnel Chest; minimally invasive repair of pectus excavatum Congenital Progressive Scoliosis; Infantile Rec 60 Adt Jan-07 Feb-12 The Alfred Sen Not yet 100 Child Apr-11 Oct-12 University of Rec Adt Aarhus Sen Rec http://ClinicalTrials.gov/show/NCT00298259 http://ClinicalTrials.gov/show/NCT01308385 250 Child Jan-08 Jan-16 Shriners http://ClinicalTrials.gov/show/NCT00689533 Hospitals for Children; Chest Wall and Spine Deformity Research Foundation 87 A5. SHOULDER (including clavicle) A5A: PAEDIATRICS Title Interventions Phases: trial design (control) CT ID Miscellaneous observational studies Elastic Stable Intramedullary Nailing of Dislocated Clavicle Fractures in Children Retrospective, cohort study NCT01325129 Youth Throwers Respond to Stretching Cross-sectional, cohort study NCT01065181 Conditions Recruit n Age Start (Grp) Date End Sponsors Date URL Dislocated Clavicular Invite 20 Child Apr-11 Dec-11 University of Fracture Treated Luebeck With Elastic Stable Intramedullary Nailing Shoulder Posterior Active, 1261 Child Jan-08 Dec-10 Metzger, Capsular NR Charles, M.D. Contracture Monly http://ClinicalTrials.gov/show/NCT01325129 Conditions URL http://ClinicalTrials.gov/show/NCT01065181 A5B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Device Outcomes Study of the TM Humeral Stem Used in Primary, Total or Hemi Shoulder Arthroplasty Prospective, cohort study NCT01480453 Interventions Device: Trabecular Osteoarthritis; Metal Humeral Stem Rheumatoid Arthritis; Post-traumatic Arthritis; Ununited Humeral Head Fracture; Irreducible 3- and 4-part Proximal Humeral Fractures; Avascular Necrosis Recruit n Rec 200 88 Age Start (Grp) Date End Sponsors Date Adt Jan-11 Dec-24 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT01480453 Outcomes Study of the TM Device: Trabecular Reverse Shoulder System Used in Metal Reverse Primary or Revision Reverse Total Shoulder System Shoulder Arthroplasty Prospective, cohort study NCT01480440 Osteoarthritis; Rheumatoid Arthritis; Post-traumatic Arthritis; Ununited Humeral Head Fracture; Irreducible 3-and 4-part Proximal Humeral Fractures; Avascular Necrosis; Gross Rotator Cuff Deficiency; Failed Total Shoulder Arthroplasty (Both Glenoid and Humeral Components Require Revision) Humeral Fractures, Proximal Treatment of Proximal Humeral Fractures Phase II: RCT, safety/efficacy study NCT01246167 Device: Philos; Device: Epoca; Other: Control group Non-Operative Versus Operative Treatment for High-Energy Midshaft Clavicle Fractures RCT NCT00590850 Device: ORIF with High Energy Plate and Screws; Midshaft Clavicle Device: Pin Fixation Fractures Rec 200 Adt Jan-11 Dec-24 Zimmer, Inc. Sen Rec 290 Invite 480 Adt Jan-11 Sep-16 Tampere http://ClinicalTrials.gov/show/NCT01246167 Sen University Hospital; Oulu University Hospital; Kuopio University Hospital; University of Tampere; Helsinki University Adt Oct-03 Dec-13 Greenville http://ClinicalTrials.gov/show/NCT00590850 Sen Hospital System University Medical Center; Orthopaedic Trauma Association; University of Tennessee; Vanderbilt University; Indiana University 89 http://ClinicalTrials.gov/show/NCT01480440 Effectiveness of Intensive Rehabilitation on Shoulder Function After Proximal Humerus Fracture RCT, efficacy study NCT01113411 Device: PHILOS™ locked plate system by Synthes Canada®; Other: Early and intensive exercise program; Other: Standard rehabilitation program Intramedullary Fixation of Humerus Device: Quantum Fractures Without Intramedullary Reaming Single group assignment, safety/efficacy study NCT01087463 Intramedullary Fixation of Humerus Device: Quantum Fractures Single group assignment, safety/efficacy study NCT01017289 Drugs including biologics Does Teriparatide (rhPTH 1-34) Drug: Teriparatide Promote Fracture Healing in Proximal Humeral Fractures? Phase IV: RCT, efficacy study NCT01105832 Effect of PTH(1-34) Treatment on Drug: rhPTH(1-34) Fracture Healing in Vivo Phase II: RCT, efficacy study NCT00741182 Fracture of Proximal Humerus Rec 80 Adt Dec-09 Oct-13 Hopital de Sen l'Enfant-Jesus Humeral Fractures; Pathological Fractures Not yet Rec 20 Adt Apr-10 Apr-12 N.M.B. Medical http://ClinicalTrials.gov/show/NCT01087463 Sen Applications Ltd Humeral Fractures; Pathological Fractures Not yet Rec 20 Adt Dec-09 Dec-11 N.M.B. Medical http://ClinicalTrials.gov/show/NCT01017289 Sen Applications Ltd Humeral Fracture Rec 40 http://ClinicalTrials.gov/show/NCT01105832 Shoulder Fractures; Trochanteric Fractures Rec A Study of rhBMP-2/CPM in Drug: rhBMP-2/CPM Fractures, Humerus (proximal, Closed Fractures of the Humerus diaphyseal) Phase II: RCT, safety/efficacy study NCT00384852 Comp Adt Apr-10 Sep-11 University Sen Hospital, Linkoeping Fonly 96 Adt Oct-08 Sep-10 Glostrup Sen University Hospital, FCopenhagen; only The Danish Medical Research Council 139 Adt Jan-07 Feb-10 Wyeth is now a Sen wholly owned subsidiary of Pfizer 90 http://ClinicalTrials.gov/show/NCT01113411 http://ClinicalTrials.gov/show/NCT00741182 http://ClinicalTrials.gov/show/NCT00384852 Procedure The Effect of the Timing of Postoperative Mobilisation After Locking Plate Osteosynthesis of Fractures of the Surgical Neck of the Humerus Phase III: RCT, efficacy study NCT01524965 Treatment of Comminuted Fractures of the Proximal Humerus. A Randomised, Controlled Study Phase III: RCT, safety/efficacy study NCT00999193 Conservative Treatment Versus the Surgical Treatment of Diaphyseal Fractures of Humerus Non-randomized, efficacy study NCT01116349 Treatment of Displaced, Midshaft Clavicle Fractures. Sling or Plate? RCT NCT01483482 Procedure: Humeral Fracture Immediate mobilisation after locking-plate osteosynthesis; Procedure: Standard mobilisation after locking plate osteosynthesis; Device: Osteosynthesis with a locking plate (Philos) Procedure: locking Humeral Fracture plate, ORIF; Procedure: Hemiarthroplasty; Other: Conservative treatment Rec 100 Adt May-11 Dec-15 Helsinki http://ClinicalTrials.gov/show/NCT01524965 Sen University; National Institute for Health and Welfare, Finland Rec 150 Adt Nov-10 Nov-14 Helsinki http://ClinicalTrials.gov/show/NCT00999193 Sen University; Helsinki University Central Hospital; National Institute for Health and Welfare, Finland Adt Jan-11 Jul-14 Hopital de http://ClinicalTrials.gov/show/NCT01116349 Sen l'Enfant-Jesus Procedure: Plate and Humeral Diaphysis Rec screws or nailing; Fracture Device: Hanging Support System (HSS) brace Procedure: Acute, Displaced Rec Conservative Midshaft Clavicle Treatment; Fractures Procedure: Surgical treatment Multi-centre randomised trial Surgery (fixation or Displaced fracture of Active evaluating surgery for displaced joint replacement); the proximal fractures of the proximal humerus Non-surgical humerus RCT management (sling ISRCTN50850043 immobilisation) 70 120 Adt Apr-11 Apr-14 Hvidovre University Hospital 250 Child Oct-08 Feb-14 University of Adt Teesside (UK) Sen 91 http://ClinicalTrials.gov/show/NCT01483482 http://www.controlledtrials.com/ISRCTN50850043 Fixation of Midshaft Fractures of the Clavicle With Plate and Intramedullary Flexible Nail Phase II: RCT, safety/efficacy study NCT01410032 Plating Clavicle Fractures RCT, efficacy study NCT00871468 Management of Displaced Supracondylar Fractures of the Humerus Using Lateral vs. Crossed K-wires RCT, safety/efficacy study NCT00358787 Procedure: Fracture Fracture of Shaft of fixation with Plate.; Clavicle Procedure: Fracture fixation with intramedullar nailing Rec 40 Procedure: superior Clavicle Fracture, plate; Procedure: Non Union/Malunion anterior-inferior plate Rec 90 Rec 42 Rec 89 Child Mar-09 Mar-13 St. Michael's Adt Hospital, Toronto http://ClinicalTrials.gov/show/NCT00872105 Rec 30 Adt Dec-09 Jan-13 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT00408291 Rec 140 Adt http://ClinicalTrials.gov/show/NCT01078480 Crossed K-wiring of Humeral Fractures supracondylar fracture of the humerus; Lateral Kwiring of supracondylar fracture of the humerus Conservative Treatment Versus Procedure: NonClavicle Fracture; Operative Plate Fixation for Acute, operative Treatment; Fractures Displaced Fractures of the Distal Procedure: Operative Clavicle Treatment RCT NCT00872105 Evaluation of Treatment of Procedure: Winsta Fracture Fractures of the Humerus With a PH osteosynthesis Plate. device Prospective, cohort study NCT00408291 Conservative Treatment Operation using a Displaced Midshaft Compared to Osteosynthesis in precontoured Fracture of the Patients With a Fractured Collar titanium plate and Collar Bone Bone screws; Displaced RCT, efficacy study midshaft fracture of NCT01078480 the collar bone treated with an arm sling 92 Child Jul-10 Adt Jul-13 University of Sao http://ClinicalTrials.gov/show/NCT01410032 Paulo Adt Oct-08 Jun-13 United States http://ClinicalTrials.gov/show/NCT00871468 Army Institute of Surgical Research; William Beaumont Army Medical Center Child Jul-08 Apr-13 University of http://ClinicalTrials.gov/show/NCT00358787 British Columbia Apr-10 Dec-12 Northern Orthopaedic Division, Denmark Simple Decompression Versus Anterior Transposition of the Ulnar Nerve RCT NCT01051869 Treatment of midshaft clavicle fractures: plate fixation versus figure-of-eight bandage. RCT ISRCTN66495030 Lateral Mini Approach vs Anterior Approach for Plating of Proximal Humerus Fracture RCT, safety/efficacy study NCT00612391 Procedure: Simple decompression; Procedure: anterior subcutaneous transposition Plate fixation; Bandage (figure of eight) Humeral Fractures; Ulnar Nerve Compression Clavicle fractures Procedure: Lateral Proximal Humerus minimally invasive Fracture approach (plate fixation); Procedure: Deltopectoral approach (plate fixation) Plate Osteosynthesis Versus ESIN Procedure: plate Clavicular Fractures of Displaced Midclavicular osteosynthesis; Fractures Procedure: ESIN Phase II: RCT, safety/efficacy study NCT01015924 The Treatment of Clavicular Procedure: Displaced, Midshaft Fractures osteosynthesis; Clavicular Fractures RCT, efficacy study Other: sling NCT00642265 Comparison of Nailing, Plate Fixation and Non-operative Treatment of Midshaft Clavicle Fractures RCT, efficacy study NCT01307670 Procedure: Operative Fracture of Clavicle treatment with intramedullary nailing; Procedure: Operative treatment with plate fixation. Other Percutaneous Versus Open Plate Other: xrays Fixation of Diaphyseal Clavicle Fractures Prospective, cohort study NCT01405703 Clavicle Fracture Rec 54 Child Sep-10 May-12 St. Michael's Adt Hospital, Toronto Comp 120 Rec 90 Rec 90 Rec 100 Adt Invite 30 Adt Sen http://ClinicalTrials.gov/show/NCT01051869 Adt Jan-08 Jan-12 Universidade http://www.controlledFederal de Sao trials.com/ISRCTN66495030 Paulo (UNIFESP) (Brazil) Adt Nov-07 Jan-12 University of http://ClinicalTrials.gov/show/NCT00612391 Sen Montreal Child Jul-09 Dec-11 University Adt Hospital, Akershus http://ClinicalTrials.gov/show/NCT01015924 Apr-08 Aug-11 University http://ClinicalTrials.gov/show/NCT00642265 Hospital, Ghent; Bart Berghs, MD - AZ Sint-Jan Brugge, Belgium Wdrwn 400 Child Apr-08 Mar-10 University of http://ClinicalTrials.gov/show/NCT01307670 Adt MissouriSen Columbia 93 Jul-11 Jul-14 University of Utah http://ClinicalTrials.gov/show/NCT01405703 Study Comparing Intramedullary Nailing, Plate Fixation, and Nonoperative Treatment of Clavicle Fractures RCT, efficacy study NCT01311219 Other: Non-operative Fracture of Clavicle Treatment; Procedure: Operative Treatment-Plate Fixation; Procedure: Operative TreatmentIntramedullary Pinning Miscellaneous observational studies A Clinical Investigation of the Copeland™ Humeral Resurfacing Head Prospective, cohort study NCT00698750 Clinical Outcomes Following Glenoid Neck Fracture as Correlated With Quantitative Assessment of Osseous Injury Prospective, cohort study NCT00644813 Validation of a Kinematic Functional Shoulder Score Including Only Essential Movements Prospective, cohort study NCT01431417 Comparison of Early and Late Therapy for Adults With NonOperatively Treated Proximal Humerus Fractures Prospective, cohort study NCT00438633 Operative Versus Non-Operative Treatment of Clavicle Fracture in PolyTrauma Prospective, case-crossover study NCT01133769 Operative Versus Nonoperative Treatment for Scapula Fractures Prospective, cohort study NCT00849771 Wdrwn 480 Child May-09 May-11 University of Adt MissouriSen Columbia http://ClinicalTrials.gov/show/NCT01311219 Osteoarthritis; Term Rheumatoid Arthritis; Avascular Necrosis; Humeral Fractures 160 Adt Apr-04 Apr-15 Biomet Sen Orthopedics, LLC Scapula Rec 50 Adt Mar-08 Dec-14 Boston Medical http://ClinicalTrials.gov/show/NCT00644813 Sen Center Rotator Cuff, Syndrome; Frozen Shoulder; Humerus, Fracture; Other Instability of Joint, Shoulder Region Proximal Humeral Fractures Rec 100 Adt Sen Rec 60 Fracture of Clavicle; Chest Injury Rec 88 Adt Jun-10 Jun-13 University of Sen Kentucky; Synthes Inc. http://ClinicalTrials.gov/show/NCT01133769 Fracture of Scapula; Fracture of Clavicle Rec 80 Adt Mar-08 Jan-13 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00849771 94 http://ClinicalTrials.gov/show/NCT00698750 Jul-11 Feb-14 Haute Ecole http://ClinicalTrials.gov/show/NCT01431417 Cantonale Vaudoise de Santé; Swiss National Science Foundation Adt Feb-05 Dec-13 Massachusetts http://ClinicalTrials.gov/show/NCT00438633 Sen General Hospital Clinical Outcome Comparison Between Medial and Lateral Offset Reverse Shoulder Arthroplasty Prospective, case-only study NCT01086202 An Algorithm for Intra-operative Goal-directed Haemodynamic Management in Non-cardiac Surgery Retrospective, cohort study NCT01384097 Rotator Cuff Injury in Antegrade Locked Nailing for Humeral Fractures Retrospective, cohort study NCT00772850 Influence of Local Bone Status on Complications After Surgical Treatment of Proximal Humerus Fractures Prospective, case-only study NCT01143675 Rotator Cuff Tear; Proximal Humerus Fractures; Malunions; Chronic Proximal Humerus Dislocations Fracture of Surgical Neck of Humerus; Colonic Tumor; Stage IIIB Ovarian Carcinoma; Neoplasm of Head of Pancreas Humeral Fractures Proximal Humeral Fractures; Poor Bone Quality; Treatment Complications Rec 40 Adt May-10 Apr-12 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT01086202 Comp 774 Adt Sep-07 Jun-11 Charite http://ClinicalTrials.gov/show/NCT01384097 Sen University, Berlin, Germany Comp 50 Child Oct-08 Jun-10 National Taiwan http://ClinicalTrials.gov/show/NCT00772850 Adt University Sen Hospital Comp 148 Adt Mar-07 Apr-10 AO Clinical http://ClinicalTrials.gov/show/NCT01143675 Sen Investigation and Documentation Recruit n Comp 100 A5C: ROTATOR CUFF PATHOLOGIES Title Interventions Phases: trial design (control) CT ID Behavioural Progressive Exercise After Behavioral: Operation of Rotator Cuff Rupture Progressive exercise and Anterior Labrum Rupture RCT, efficacy study NCT00624117 Conditions Rotator Cuff Disease; Shoulder Joint 95 Age Start (Grp) Date End Sponsors Date URL Adt May-06 Feb-10 Jyväskylä http://ClinicalTrials.gov/show/NCT00624117 Central Hospital Device Long-term Clinical Effectiveness of Device: Delta Xtend the Delta Xtend Reverse Total Reverse Total Shoulder Shoulder Phase IV: Single group assignment, safety/efficacy study NCT00737087 RSP® Prospective Multi-Center Study Phase IV: Prospective, cohort study NCT01005446 Prospective Study for Safety and Efficacy of SpaceGuard™ in Rotator Cuff Tear Subjects Single group assignment, safety/efficacy study NCT00916994 Outcomes in Rotator Cuff Repair Using Graft Reinforcement Phase IV: Single group assignment, efficacy study NCT01025037 Post-Operative Quality of Life Evaluation for Different Anesthesia Techniques for Arthroscopic Shoulder Surgery RCT, efficacy study NCT01355757 Effectiveness of the Ivivi Torino II, Pulsed Radio Frequency Device, on Narcotic Use, Pain and Quality of Life Following Shoulder Arthroscopic Rotator Cuff Repair. RCT, safety/efficacy study NCT01507818 Cuff Tear Arthropathy; Osteoarthritis With Cuff Deficiency; Rheumatoid Arthritis; Post Traumatic Injury to Shoulder; Revision Surgery of a Failed Anatomic Shoulder Prosthesis Device: Encore Rotator Cuff Reverse Shoulder Deficiency; Shoulder Prosthesis (RSP®) Arthropathy; Failed Shoulder Replacement Device: SpaceGuard Rotator Cuff Tear Balloon Rec 250 Adt Oct-07 Mar-19 DePuy Sen International Rec 224 Adt Dec-09 Jan-18 Encore Medical, http://ClinicalTrials.gov/show/NCT01005446 Sen L.P. Rec 70 Adt Sen Device: Conexa Reconstructive Tissue Matrix Rotator Cuff Tear Rec 65 Adt Oct-09 Oct-13 Tornier; LifeCell http://ClinicalTrials.gov/show/NCT01025037 Sen Device: Baxter INFUSOR System Rotator Cuff Injury Not yet 100 Rec Device: Ivivi Torino II; Device: Inactive Sham device Rotator Cuff Tear Adt Jun-11 Jun-12 St. Luke'shttp://ClinicalTrials.gov/show/NCT01355757 Sen Roosevelt Hospital Center; Baxter Healthcare Corporation Adt Dec-11 May-12 Amp http://ClinicalTrials.gov/show/NCT01507818 Sen Orthopedics, Inc. Rec 102 96 Jul-09 Dec-14 BioProtect http://ClinicalTrials.gov/show/NCT00737087 http://ClinicalTrials.gov/show/NCT00916994 Rotator Cuff Repair (RCR) With and Without OrthoADAPT Augmentation Single group assignment, efficacy study NCT00957255 Pilot Study of Augment Rotator Cuff for Surgical Treatment of Full Thickness Rotator Cuff Tears Phase I: RCT, safety study NCT01256242 Use of Graft Jacket for Rotator Cuff Repair Phase II: RCT, safety/efficacy study NCT00456781 Drugs including biologics The Influence of Growth Factors (PDGF), Applied as Autologous Thrombocyte Concentrate, on Functional Recovery Phase III: RCT, efficacy study NCT01510639 A Safety Study Of BMP-655/ACS As An Adjuvant Therapy For Treatment Of Rotator Cuff Tears Phase I: RCT, safety study NCT01122498 Plasma Glucose Levels With Dexamethasone as Adjuvant to Interscalene Block Phase III: RCT, pharmacokinetics study NCT01538459 Device: Rotator Cuff Tear OrthoADAPT; Procedure: Standard of care Term 90 Adt Mar-09 Jan-12 Synovis Surgical http://ClinicalTrials.gov/show/NCT00957255 Sen Innovations Device: Augment Full Thickness Rotator Cuff; Rotator Cuff Tear Procedure: Standard Suture Repair Active, NR 30 Adt Nov-10 Dec-11 BioMimetic Sen Therapeutics Device: Augmentation; Procedure: Rotator Cuff Repair without augmentation Rotator Cuff Tear Active, NR 160 Adt Apr-07 Jul-10 Fowler Kennedy http://ClinicalTrials.gov/show/NCT00456781 Sen Sport Medicine Clinic; Wright Medical Technology Biological: Platelet Rich Plasma Rotator Cuff Rupture; Subacromial Impingement Rec 104 Adt Sen Biological: BMP655/ACS+Standard of care or Standard of care; Biological: BMP655/ACS+Standard of care or Standard of care; Biological: BMP655/ACS+Standard of care or Standard of care Drug: Dexamethasone; Drug: Bupivacaine Rotator Cuff Tear Active, NR 42 Adt Jun-10 Apr-13 Pfizer Sen Shoulder Pain; Injury Not yet 100 of Shoulder Region; Rec Disorder of Shoulder; Disorder of Rotator Cuff; Disorder of Tendon of Biceps 97 Jul-10 Dec-13 St. Antonius Hospital http://ClinicalTrials.gov/show/NCT01256242 http://ClinicalTrials.gov/show/NCT01510639 http://ClinicalTrials.gov/show/NCT01122498 Adt Apr-12 Apr-13 Lifespan; Tufts http://ClinicalTrials.gov/show/NCT01538459 Sen Medical Center; United States Naval Medical Center, Portsmouth Ropivacaine Block Alone or With Perineural or Systemic Dexamethasone for Pain in Shoulder Surgery Phase III: RCT, efficacy study NCT01450007 Platelet rich plasma and rotator cuff tendons RCT ISRCTN10464365 Drug: Ropivacaine; Drug: Dexamethasone; Drug: Dexamethasone; Drug: Normal saline; Drug: Normal saline Subacromial decompression; Subacromial decompression and platelet-rich plasma Biological: Plateletrich plasma (PRP) therapy Interscalene Not yet 120 Blockade in Elective Rec Arthroscopic Rotator Cuff Repair Adt Nov-11 Feb-13 Mayo Clinic Sen http://ClinicalTrials.gov/show/NCT01450007 Rotator cuff impingement and tears Platelet-Rich Plasma Therapy for Shoulder Pain; Shoulder Pain in Persons With Rotator Cuff Spinal Cord Injury Tendinitis; Rotator Phase I: Single group Cuff Syndrome; assignment, safety/efficacy Spinal Cord Injury study NCT01355549 Treatment of the Rotator Cuff Biological: platelet Subacromial Disease With Platelet Rich Plasma rich plasma injection; Impingement Injection Drug: corticosteroid Syndrome; Partial RCT, efficacy study injection Thickness Rotator NCT01123889 Cuff Tear The use of platelet-leukocyte Arthroscopic rotator Large Rotator cuff membrane in arthroscopic repair of cuff repair ± platelet- tear large rotator cuff tear leukocyte membrane RCT ISRCTN93082180 Hyaluronic acid versus Hyaluronic acid; Subacromial corticosteroids compared to a corticosteroids; impingement placebo in subacromial injections placebo syndrome. for shoulder cuff impingement RCT, efficacy study ISRCTN51511455 Post-Op Rotator Cuff Pain Study Drug: 0.5% Rotator Cuff Tear With Subacromial Bupivacaine bupivacaine; Drug: Infusion Normal Saline RCT, efficacy study NCT01126593 Active 34 Adt Oct-10 Sep-12 University of Sen Oxford (UK) http://www.controlledtrials.com/ISRCTN10464365 Rec 6 Adt May-11 Jul-12 Kessler Foundation http://ClinicalTrials.gov/show/NCT01355549 Comp 12 Adt May-10 May-11 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT01123889 Comp 80 http://www.controlledtrials.com/ISRCTN93082180 Comp 159 Adt May-08 Oct-10 Orthopaedic Sen Clinic University of Rome "Sapienza" (Italy) Adt Oct-04 Mar-10 Care and Public Sen Health Research Institute (CAPHRI) (The Netherlands) Comp 89 98 http://www.controlledtrials.com/ISRCTN51511455 Adt Dec-08 Feb-10 Orlando Health, http://ClinicalTrials.gov/show/NCT01126593 Sen Inc. Procedure Early Mobilization Following Arthroscopic Rotator Cuff Repair Phase IV: RCT, efficacy study NCT01333527 Latissimus Dorsi Tendon Transfer or Partial Arthroscopic Repair of Massive Rotator Cuff Tears RCT NCT01481480 United Kingdom Rotator Cuff Trial RCT ISRCTN97804283 Comparison of Tendon Repair and Physiotherapy in the Treatment of Small and Medium-sized Tears of the Rotator Cuff RCT NCT00852657 Incidence of Brachial Plexus Injury After Rotator Cuff Repair With Continuous Interscalene Block RCT, safety study NCT01334632 Arthroscopic Rotator Cuff Repair With Platelet-Rich Plasma (PRP) in Medium to Large Rotator Cuff Tears RCT, efficacy study NCT01458665 Procedure: No Sling; Rotator Cuff Tear Procedure: Sling Procedure: Latissimus dorsi tendon transfer; Procedure: Arthroscopic repair Full Thickness Rotator Cuff Tear Open/mini-open Rotator cuff tear surgery; Arthroscopic surgery Procedure: Tendon Rotator Cuff Tear repair with acromioplasty; Procedure: Physiotherapy Procedure: Brachial Plexus Continuous Injury interscalene block; Procedure: PCA morphine Procedure: Rotator Cuff Tear Conventional arthroscopic rotator cuff repair; Procedure: Arthroscopic rotator cuff repair with PRP Rec 200 Not yet 108 Rec Active 690 Active, NR 103 Adt Apr-11 Dec-16 Shoulder & http://ClinicalTrials.gov/show/NCT01333527 Sen Upper Extremity Research Group of Edmonton Adt May-12 Jan-14 St. Michael's http://ClinicalTrials.gov/show/NCT01481480 Hospital, Toronto; University Health Network, Toronto; Sunnybrook Health Sciences Centre Adt Jul-07 Dec-13 University of http://www.controlledSen Oxford (UK) trials.com/ISRCTN97804283 Adt Sep-04 Dec-13 Martina Sen Hansen's Hospital Rec 120 Child Apr-11 Nov-13 Centre Adt Hospitalier Sen Universitaire Vaudois Rec 74 99 Adt Oct-11 Oct-13 Seoul National Sen University Hospital http://ClinicalTrials.gov/show/NCT00852657 http://ClinicalTrials.gov/show/NCT01334632 http://ClinicalTrials.gov/show/NCT01458665 Subacromial impingement syndrome and pain: a randomised controlled trial of exercise and injection (the SUPPORT trial) RCT ISRCTN42399123 Ultrasound-guided corticosteroid injection OR Unguided corticosteroid injection WITH EITHER physiotherapist-led individualised, supervised & progressed exercise OR an advice & exercise leaflet Study of 25% Dextrose Injections Procedure: shoulder in Shoulder Ligaments and injections Tendons to Promote Their Healing RCT, efficacy study NCT01402011 The Clinical Efficacy of Belting Procedure: Stabilization for Shoulder Pain Stabilization belt; Phase I: RCT, efficacy study Procedure: NCT00826293 Stabilization belt Arthroscopic Rotator Cuff Repair Procedure: With Platelet-Rich Plasma(PRP) in Conventional Large to Massive Tears arthroscopic rotator RCT, efficacy study cuff repair; NCT01238302 Procedure: Arthroscopic rotator cuff repair with PRP Distal Clavicle Resection With Procedure: distal Rotator Cuff Repair clavicle resection Prospective, case control study NCT01040065 All-Arthroscopic Versus Mini-Open Procedure: AllRepair of Small or Moderate Arthroscopic repair; Rotator Cuff Tears Procedure: MiniPhase III: RCT, efficacy study open repair NCT00128076 Subacromial impingement syndrome Active 252 Adt Mar-11 Sep-13 Keele University http://www.controlledSen (UK) trials.com/ISRCTN42399123 Rotator Cuff Tendinitis Rec 75 Adt Nov-10 Jun-13 University of http://ClinicalTrials.gov/show/NCT01402011 Sen British Columbia Rotator Cuff Impingement Syndrome Invite 64 Adt Rotator Cuff Tear Rec 48 Adt Nov-10 Dec-12 Seoul National Sen University Hospital http://ClinicalTrials.gov/show/NCT01238302 Acromioclavicular Joint Arthritis Rec 60 Child Jun-08 Mar-12 Samsung Adt Medical Center Sen http://ClinicalTrials.gov/show/NCT01040065 Shoulder Pain; Rotator Cuff Tear Rec 225 Adt Aug-06 Dec-11 McMaster Sen University; Canadian Institutes of Health Research; The Physicians' Services Incorporated Foundation http://ClinicalTrials.gov/show/NCT00128076 100 Jan-09 Feb-13 Sunnybrook http://ClinicalTrials.gov/show/NCT00826293 Health Sciences Centre Types of Fixation in Arthroscopic Procedure: single Rotator Cuff Tear Rotator Cuff Repair row; Procedure: RCT, efficacy study double row fixation NCT00508183 Rotator Cuff Repair With Procedure: without Shoulder Injuries Arthroscopic Acromioplasty acromioplasty; (Shaving the Acromion Bone) Procedure: with Versus Repair Without acromioplasty Acromioplasty RCT, safety/efficacy study NCT00664794 Arthroscopic Rotator Cuff Repair of Procedure: Rotator Cuff Full Thickness Tears With and Acromioplasty Syndrome; Shoulder Without Arthroscopic Impingement Acromioplasty Syndrome RCT, efficacy study NCT00290888 Arthroscopic Rotator Cuff Repair Procedure: Rotator Cuff Tear With Multimodal Analgesia(MMA) Arthroscopic rotator RCT, efficacy study cuff repair with NCT01204606 intraoperative periarticular injection; Procedure: Arthroscopic rotator cuff repair with noninjection of MMA drugs Accuracy of Needle Placement Procedure: Injection Rotator Cuff Into The Subacromial Space of of Subacromial Tendonitis The Shoulder Bursa RCT, efficacy study NCT01330641 Other The Effect of Systemic or Perineural Dexamethasone on the Duration of Interscalene Nerve Blocks With Ropivacaine RCT, efficacy study NCT01495624 Other: ropivacaine plus dexamethasone anesthetic; Other: ropivacaine plus saline plus dexamethasone anesthetic Duration of Interscalene Block; Rotator cuff repair or subacromial decompressio Comp 80 Child Apr-07 Jul-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00508183 Adt Research Sen Institute Comp 48 Adt Oct-06 Apr-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00664794 Sen Research Institute Comp 86 Adt Apr-04 Mar-11 Panam Clinic Sen http://ClinicalTrials.gov/show/NCT00290888 Comp 54 Adt Sep-10 Mar-11 Seoul National Sen University Hospital http://ClinicalTrials.gov/show/NCT01204606 Comp 75 Adt Sep-08 Mar-11 University of http://ClinicalTrials.gov/show/NCT01330641 Sen California, Davis Rec 438 Adt Dec-11 Jan-15 The Cleveland Sen Clinic 101 http://ClinicalTrials.gov/show/NCT01495624 Does Autologous Conditioned Plasma Enhance Rotator Cuff Tendon Healing After Surgery? Phase III: RCT NCT01414764 Impact of Autologous Platelet Rich Plasma on Healing of Rotator Cuff Repairs Phase II/III: RCT, safety/efficacy study NCT01000935 Other: Autologous Supraspinatus Tear conditioned plasma (ACP); Drug: Placebo Invite 60 Adt May-11 Apr-13 The University of http://ClinicalTrials.gov/show/NCT01414764 Sen Western Australia; Arthrex, Inc. Other: Platelet Rich Rotator Cuff Plasma; Other: Pathology Platelet Rich plasma Rec 80 Other: Platelet rich plasma Rec 40 Adt Mar-11 Mar-13 Sunnybrook http://ClinicalTrials.gov/show/NCT01000935 Sen Health Sciences Centre; Hand and Upper Limb Clinic, Canada; St. Joseph's Health Care London Adt Sep-08 Sep-12 University of Sao http://ClinicalTrials.gov/show/NCT01029574 Sen Paulo; Criogenesis Platelet Rich Plasma on Rotator Cuff Repair Phase III: RCT, efficacy study NCT01029574 Arthroscopic Surgical Outcome Study In Subjects With Rotator Cuff Tears Phase I: Prospective, cohort study NCT00739947 Post-op Rehabilitation's Influence on Tendon Healing & Clinical Outcomes Following Arthroscopic Rotator Cuff Repair RCT, safety/efficacy study NCT00756015 Rotator Cuff Lesions Other: Observational Rotator Cuff; Comp study of the surgical Arthroscopic Surgery outcome 162 Adt Oct-08 Jul-11 Pfizer Sen http://ClinicalTrials.gov/show/NCT00739947 Other: Early Motion Protocol; Other: Immobilization Miscellaneous observational studies Results of Rotator Cuff Repair Retrospective, case control study NCT01549912 Features to Predict Success With Nonoperative Treatment of Patients With Rotator Cuff Tears Prospective, cohort study NCT00762580 Rotator Cuff Tear Invite 140 Adt Nov-07 Dec-10 Washington University School of Medicine; Barnes-Jewish Hospital Foundation http://ClinicalTrials.gov/show/NCT00756015 Acute Shoulder Dislocation Invite 40 Adt Feb-12 Feb-15 University of Sen Utah http://ClinicalTrials.gov/show/NCT01549912 Active, NR 380 Adt Jan-06 Jan-14 Vanderbilt Sen University (US) http://ClinicalTrials.gov/show/NCT00762580 Rotator Cuff Tear 102 Validation of the Western Ontario Rotator Cuff Index in Patients With Arthroscopic Rotator Cuff Repair Prospective, cohort study NCT01532492 Results of Shoulder Arthroscopic Surgery for Rotator Cuff, Biceps Tendon, Labrum and Capsule Retrospective study NCT01401738 Functional Outcomes Following Shoulder Surgery: A Prospective Database Prospective study NCT00253864 The Effects of Platelet Rich Plasma on the Integrity of Rotator Cuff Repair Prospective, cohort study NCT01424969 Assessment of Muscle Function and Size in Older Adults With Rotator Cuff Tear Prospective, case control study NCT01459536 Follow Up Study of Tear in the Rotator Culf Cross-sectional, case-crossover study NCT00589433 Analysis of Proinflammatory Factors in the Synovial Fluid In Patients With Rotator Cuff Disease Prospective, cohort study NCT01069224 Outcomes After Repair of Acute Rotator Cuff Tears Retrospective, case-only study NCT01140230 Rotator Cuff Lesion; Disorder of Rotator Cuff; Other Instability, Shoulder Rec 90 Adt Nov-11 Jun-13 St. Antonius Sen Hospital http://ClinicalTrials.gov/show/NCT01532492 Shoulder Active, Arthroscopic Surgery NR 170 Adt May-11 May-13 Taipei Medical Sen University WanFang Hospital http://ClinicalTrials.gov/show/NCT01401738 Rotator Cuff Tear; Osteoarthritis; Shoulder Instability 2500 Adt Nov-04 Jan-13 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00253864 Sen Research Institute Rec Rotator Cuff Tear Arthropathy Active, NR 50 Adt Aug-08 Aug-12 University of Sen Utah http://ClinicalTrials.gov/show/NCT01424969 Rotator Cuff Tear Rec 50 Adt Sep-11 Feb-12 Wake Forest Sen University http://ClinicalTrials.gov/show/NCT01459536 Rotator Culf Tear Not yet Rec 50 Adt Jun-11 Dec-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00589433 Rotator Cuff Disease Not yet Rec 40 Adt Mar-10 Mar-11 Tel-Aviv Sourasky Medical Center http://ClinicalTrials.gov/show/NCT01069224 Rotator Cuff Tear 42 Adt Aug-09 May-10 University Sen Hospital, Linkoeping http://ClinicalTrials.gov/show/NCT01140230 Comp 103 A5D: OTHER Title Interventions Phases: trial design (control) CT ID Behavioural Biopsychosocial Factors' Influence Behavioral: pain on Shoulder Pain perception Prospective, case-only study NCT00187863 Device Clinical Experience With the Zimmer Trabecular Metal (TM) Glenoid in Total Shoulder Arthroplasty RCT NCT01539122 Humeral Resurfacing Hemiarthroplasty Single group assignment, efficacy study NCT00477360 Open-Label Study for Shoulder Dislocation Using MG-1 Phase III: Single group assignment, safety/efficacy study NCT01528319 Global® AP™ Total Shoulder Arthroplasty Single group assignment, efficacy study NCT00719771 Pulsed Electromagnetic Fields (PEMF) and Post-Axillary Surgery Morbidity Phase IV: RCT, efficacy study NCT01255631 Conditions Recruit n Pain Assessment Active, NR 350 Adt May-05 May-11 University of Sen Florida http://ClinicalTrials.gov/show/NCT00187863 Device: Zimmer TM Osteoarthritis of the Glenoid; Device: Shoulder Cemented Glenoid Not yet Rec 80 Adt Feb-12 Feb-20 Joint Sen Preservation Centre of BC http://ClinicalTrials.gov/show/NCT01539122 Device: Humeral Advanced surface replacement Glenohumeral hemiarthroplasty Arthritis (CAP) Active, NR 30 Invite 24 Child Jan-07 Feb-13 University of http://ClinicalTrials.gov/show/NCT00477360 Adt Calgary; DePuy Sen International; Johnson & Johnson Adt Dec-11 Jan-13 Johnson & http://ClinicalTrials.gov/show/NCT01528319 Johnson K.K. Medical Company Device: Total Osteoarthritis shoulder arthroplasty (Global® AP™ Shoulder) Rec 120 Adt Jan-08 Dec-12 DePuy Sen Orthopaedics Device: PEMF Shoulder Symptoms Device; Device: After Lymph Node Sham PEMF Device Dissection Rec 60 Adt Nov-10 Aug-12 Columbia http://ClinicalTrials.gov/show/NCT01255631 Sen University; Ivivi Health Sciences, FLLC only Device: MG-1 Shoulder Dislocation 104 Age Start (Grp) Date End Sponsors Date URL http://ClinicalTrials.gov/show/NCT00719771 This is a 2 Year Follow up Clinical Device: Shoulder and Radiographic Analysis of a arthroplasty with Novel All Polyethelene Glenoid anchor peg glenoid Component in Standard Total Shoulder Arthroplasty. Phase IV: Single group assignment, safety/efficacy study NCT01313741 Columbia Shoulder Study (CSS) Device: Phase IV: Single group Bigliani/Flatow assignment, safety/efficacy Shoulder System study NCT01488006 Splintage In External Rotation For Current practice Anterior Glenohumeral Dislocation: (Sling); external A Prospective, Randomised & rotation splint Controlled Study RCT ISRCTN41070054 Conform and non conform glenoid Conform glenoid components in total shoulder component; nonreplacements conform glenoid RCT, efficacy study component ISRCTN42881741 ORTHOVISC Shoulder RCT Device: Phase III: RCT, safety/efficacy ORTHOVISC study NCT00436969 Drugs including biologics AA4500 for the Treatment of Adhesive Capsulitis of the Shoulder Phase II: RCT, safety/efficacy study NCT01483963 Can Parecoxib Reduce Postoperative Ipsilateral Shoulder Pain? Phase II: RCT, safety/efficacy study NCT01288924 The Primary Disease Not yet 200 Process Being Rec Studied is Shoulder OA and the Effect of an All Polyethelene Glenoid Component on Shoulder Arthroplasty Adt Apr-11 Apr-12 Knoxville Sen Orthopedic Clinic http://ClinicalTrials.gov/show/NCT01313741 Glenohumeral Osteoarthritis Comp 207 Adt Apr-01 Dec-11 Columbia Sen University; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01488006 Anterior shoulder dislocation Comp 50 Child Nov-05 Nov-11 Department of Adt Health (UK) http://www.controlledtrials.com/ISRCTN41070054 Shoulder disorders due to osteoarthritis or rheumatoid arthritis. Comp 20 http://www.controlledtrials.com/ISRCTN42881741 Glenohumeral Osteoarthritis Comp 270 N/K Nov-06 Nov-10 Leiden University Medical Center (LUMC) (The Netherlands) Adt Dec-06 Aug-11 DePuy Mitek Sen http://ClinicalTrials.gov/show/NCT00436969 Biological: collagenase clostridium histolyticum; Other: Shoulder exercises Adhesive Capsulitis; Frozen Shoulder Rec 50 Adt Nov-11 Feb-13 Auxilium http://ClinicalTrials.gov/show/NCT01483963 Sen Pharmaceuticals Drug: Parecoxib; Drug: Placebo Shoulder Pain; Postoperative Pain Rec 160 Adt Feb-11 Jan-13 Chiang Mai University 105 http://ClinicalTrials.gov/show/NCT01288924 Dexamethasone for Pain After Shoulder Surgery Phase IV: RCT, efficacy study NCT01414569 Drug: Dexamethasone Shoulder Impingement Syndrome; Arthritis Rec 75 Partial Tear of Supraspinatus Biological: PRGF; Partial (SSP) and Treatment With Plasma Other: NACL Supraspinatus Tear Rich in Growth Factors (PRGF) Phase I: RCT, efficacy study NCT01152658 Colchicine Treatment for Chronic Drug: Colchicine; Calcific Tendonitis Shoulder Pain Related to Calcific Drug: lactose Tendonitis RCT, efficacy study NCT00983177 Oral Clonidine & Gabapentin: Drug: Sugar pill; Shoulder Improving Recovery and Pain Drug: Gabapentin; Arthroscopy; Knee Management After Outpatient With Drug: Clonidine Arthroscopy Major Orthopedic Surgery Phase IV: RCT, efficacy study NCT01112878 A Phase 2a Study to Evaluate the Drug: AZX100 Drug Scar Prevention; Safety and Efficacy of AZX100 Product; Drug: Saline Scar Reduction Drug Product in Trocar Sites of placebo Arthroscopic Shoulder Surgery Patients Phase II: RCT, safety/efficacy study NCT00811577 Pre-operative Preparation Using Drug: 2% Post-operative 2% Chlorhexidine Cloth For Chlorhexidine cloth Surgical Site Shoulder Surgery Infections RCT, efficacy study NCT01090479 Continuous Subacromial Drug: bupivacaine Shoulder Bupivacaine Arthroscopy RCT, efficacy study NCT01377415 Rec 40 Rec 80 Adt Mar-10 Oct-11 Bnai Zion Sen Medical Center http://ClinicalTrials.gov/show/NCT00983177 Invite 180 Adt Sep-09 Jun-11 Cedars-Sinai Sen Medical Center http://ClinicalTrials.gov/show/NCT01112878 Comp 153 Adt Jan-09 Dec-10 Capstone Sen Therapeutics http://ClinicalTrials.gov/show/NCT00811577 Comp 100 Adt Jan-10 Oct-10 Northwestern http://ClinicalTrials.gov/show/NCT01090479 Sen University; Sage Products Comp 90 Adt Jan-09 Jun-10 Turku University http://ClinicalTrials.gov/show/NCT01377415 Sen Hospital 106 Adt Nov-11 Nov-12 University of http://ClinicalTrials.gov/show/NCT01414569 Sen Aarhus; Horsens Hospital; Central Denmark Region; The Family Hede Nielsens Fund; The Danish Rheumatism Association Adt Apr-10 Jun-12 Meir Medical http://ClinicalTrials.gov/show/NCT01152658 Center The Effect of Interscalene Peripheral Nerve Block With 0.25% Bupivacaine vs 0.125% Bupivacaine on Lung Function RCT, safety/efficacy study NCT01429584 Drug: interscalene nerve block Diaphragm Paralysis Comp 30 Adt May-08 Feb-10 University of Sen Utah http://ClinicalTrials.gov/show/NCT01429584 Active 60 Adt Mar-12 Mar-24 Paracelsus Medical University (Austria) http://www.controlledtrials.com/ISRCTN85886529 Active, NR 70 Adt Mar-97 May-20 University of Sen Florida http://ClinicalTrials.gov/show/NCT00160784 Not yet Rec 94 Adt Sep-11 Sep-18 AO Clinical http://ClinicalTrials.gov/show/NCT01288066 Sen Investigation and Documentation; Synthes GmbH Rec 100 Procedure: Copeland Osteoarthritis or Global CAP resurfacing prosthesis Rec 60 Adt Jun-08 Dec-17 Central Finland http://ClinicalTrials.gov/show/NCT00637013 Sen Hospital District; Academy of Finland; National Istitute For Health and Welfare, Finland Adt Dec-06 Jan-17 University of http://ClinicalTrials.gov/show/NCT00408096 Sen Aarhus Procedure: Bankart Other Instability, repair and Shoulder; Hill-Sachs remplissage; Lesion Procedure: Bankart repair Rec 150 Procedure J-bone graft versus Latarjet RCT ISRCTN85886529 Latarjet procedure; J- Post-traumatic bone graft procedure recurrent anterior shoulder instability with significant glenoid defect Arthroscopy and Manipulation vs a Procedure: Adhesive Capsulitis Home Therapy Program in the Arthroscopy; of the Shoulder Treatment of Adhesive Capsulitis Procedure: Phase IV: RCT, efficacy study Arthroscopic NCT00160784 manipulation; Other: Home therapy Effectiveness of Hemi- Versus Procedure: Osteoarthritis Total Shoulder Arthroplasty Using Hemiarthroplasty; Implants of the “Epoca” System" Procedure: Total RCT, efficacy study arthroplasty NCT01288066 Operative Versus Non-operative Procedure: Surgery Subacromial Management of Subacromial (Subacromial Impingement Impingement decompression); Syndrome RCT, efficacy study Procedure: NonNCT00637013 operative treatment (Physical therapy) Comparison of Two Resurfacing Prostheses in the Treatment of Osteoarthritis of the Shoulder RCT, efficacy study NCT00408096 Arthroscopic Bankart Repair With and Without Remplissage in Anterior Shoulder Instability Phase II: RCT, efficacy study NCT01324531 107 Adt Mar-11 Mar-15 Panam Clinic; http://ClinicalTrials.gov/show/NCT01324531 Sen University of Ottawa; University of Western Ontario, Canada; University of British Columbia A Comparison of Indirect and Direct MR Arthrography of the Shoulder Using Arthroscopic Correlation Single group assignment, efficacy study NCT01416740 Pain Management After Shoulder Prosthesis: A Clinical Trial of Nerve Block and Local Infiltration RCT, efficacy study NCT01362075 Procedure: Indirect Shoulder Pain MRA of shoulder; Drug: Gadopentetate Dimeglumine Rec 40 Adt Dec-09 Dec-13 Milton S. http://ClinicalTrials.gov/show/NCT01416740 Sen Hershey Medical Center Procedure: Local Pain, Postoperative infiltration analgesia; Procedure: Interscalene catheter Rec 80 Adt Sen New Prophylactic Maneuver: the “Pushing” Maneuver Aiming to Reduce the Risk for Shoulder Dystocia" RCT, efficacy study NCT01297439 Comparison of Two Methods of Subscapularis Management in Shoulder Arthroplasty: Tenotomy Versus Peel RCT, efficacy study NCT01404143 Non-operative Versus Operative Treatment of Acute Acromioclavicular Joint Dislocation RCT NCT00594841 Procedure: suctioning of fetal nose and mouth during delivery; Procedure: Pushing maneuver Procedure: Subscapularis Tenotomy; Procedure: subscapularis peel Rec 80 Adt Aug-11 Aug-13 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01404143 Sen Research Institute Shoulder Dystocia,; Brachial Plexus Injury; Asphyxia,; Hematoma,; Clavicle Fracture,; Humerus Fracture. Subscapularis Injury Rec Procedure: Open Shoulder Dislocation Active, Reduction Internal NR Fixation of AC joint dislocation; Other: Non operative treatment of AC joint dislocation (sling) Jul-11 Dec-13 Horsens http://ClinicalTrials.gov/show/NCT01362075 Hospital; University of Aarhus; Aarhus University Hospital; The Family Hede Nielsens Fund; Central Denmark Region; The Danish Rheumatism Association 3700 Adt Mar-11 Nov-13 Assistance http://ClinicalTrials.gov/show/NCT01297439 Publique FHôpitaux de only Paris 122 Child Jan-08 Jan-13 St. Michael's http://ClinicalTrials.gov/show/NCT00594841 Adt Hospital, Toronto; Orthopaedic Trauma Association; Osteosynthesis & Trauma Care 108 Intra-articular Injection of Allogeneic Platelet Rich Plasma (PRP) for Adhesive Capsulitis RCT, efficacy study NCT01458691 Procedure: Isotonic Adhesive Capsulitis saline injection into the glenohumeral joint; Procedure: Allogenic PRP injection into the glenohumeral joint SLAP Lesions; a Comparison of Procedure: labral SLAP Lesions Conservative and Operative repair; Procedure: Treatment. A Prospective, biceps tenodesis; Randomized Study Procedure: RCT diagnostic NCT00586742 arthroscopy Decreasing Upper and Shoulder Procedure: Shoulder Pain; Pain After Laparoscopic Surgery Pulmonary Nausea Phase III: RCT, safety/efficacy recruitment study; maneuver; NCT01433874 Procedure: Intraperitoneal normal saline infusion; Procedure: combined group; Procedure: Control group Tightrope Fixation of Procedure: Tightrope Acromioclavicular Acromioclavicular Joint Dislocation fixation Joint Dislocation - a Prospective Series Single group assignment, efficacy study NCT01274884 Changes of Body Temperature Procedure: heated Hypothermia During Shoulder Arthroscopy circuit; Procedure: RCT, safety/efficacy study control NCT01493700 Physical Therapy Versus Steroid Procedure: Manual Shoulder Injection for Shoulder Impingement Physical Therapy; Impingement Syndrome Procedure: Syndrome RCT, efficacy study Corticosteroid NCT01190891 Injection Rec 54 Adt Nov-11 Dec-12 Seoul National Sen University Hospital http://ClinicalTrials.gov/show/NCT01458691 Rec 120 Adt http://ClinicalTrials.gov/show/NCT00586742 Rec 200 Adt Feb-11 Dec-12 Taipei Veterans http://ClinicalTrials.gov/show/NCT01433874 Sen General Hospital,Taiwan; FNational Yang only Ming University Rec 25 Adt Mar-10 Dec-12 Sykehuset Asker http://ClinicalTrials.gov/show/NCT01274884 Sen og Baerum Not yet Rec 50 Adt Dec-11 Nov-12 Gachon University Gil Medical Center Rec 104 Adt May-10 Sep-12 Madigan Army http://ClinicalTrials.gov/show/NCT01190891 Sen Medical Center; University of Puget Sound; Franklin Pierce University 109 Jan-08 Dec-12 Lovisenberg Diakonale Hospital http://ClinicalTrials.gov/show/NCT01493700 Surgery or Capsular Distention With Steroid in the Treatment of Primary Frozen Shoulder? RCT NCT01029600 Procedure: Arthroscopic capsular release; Procedure: Distention with steroid Adhesive Capsulitis Rec 100 Effects of Interscalene Brachial Plexus Nerve Blocks on the Hand and Forearm Prospective, case-only study NCT01229683 Comparative Analysis of Intraarticular Injection of Steroid and/or Sodium Hyaluronate in Adhesive Capsulitis RCT, efficacy study NCT01144533 Procedure: Interscalene Nerve Block Shoulder Surgery; Interscalene Nerve Block Comp 62 Adhesive Capsulitis Rec 60 Adt Jun-10 Dec-11 Seoul National Sen University Hospital Tenotomy; Morselized Osteotomy Active, NR 80 Adt Nov-06 Dec-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00508105 Sen Research Institute Total Shoulder Arthroplasty Active, NR 34 Child Aug-10 Nov-11 The Cleveland Adt Clinic Sen Procedure: isotonic saline injection into the glenohumeral joint; Procedure: steroid injection into the glenohumeral joint; Procedure: sodium hyaluronate injection into the glenohumeral joint; Procedure: steroid and hyaluronate injection into the glenohumeral joint; Procedure: intraarticular injection of the glenohumeral joint Comparing Two Surgical Methods Procedure: of Fixation of Subscapularis During tenotomy; Shoulder Arthroplasty Procedure: RCT, efficacy study osteotomy NCT00508105 Patient Specific Instruments Procedure: Glenoid Versus Standard Surgical Positioning System Instruments Phase I: RCT, efficacy study NCT01430468 110 Adt Dec-09 Apr-12 Bergen Surgical http://ClinicalTrials.gov/show/NCT01029600 Sen Hospital; Haraldsplass Deaconess Hospital; Haukeland University Hospital Adt Oct-10 Mar-12 University of http://ClinicalTrials.gov/show/NCT01229683 Sen California, San Diego http://ClinicalTrials.gov/show/NCT01144533 http://ClinicalTrials.gov/show/NCT01430468 Followup of Glenoid Fix Utilizing Auto Bone Graft in Shoulder Replacement Retrospective, case control study NCT00670852 Subacromial Impingement - The Need of Arthroscopic Subacromial Decompression After Eccentric Physical Therapy Exercises RCT, efficacy study NCT01037673 Arthroscopic Rotator Interval Closure in Shoulder Instability Repair RCT, efficacy study NCT00901797 Analysis of the Fixation of the Proximal Biceps Tendon Retrospective, cohort study NCT01317771 Concomitant Biceps Tenodesis in Primary Shoulder Arthroplasty for Primary Osteoarthritis - A Randomised Controlled Study RCT ISRCTN71203361 Arthroscopic Versus Open Stabilization for Traumatic Shoulder Instability RCT, efficacy study NCT00251264 Procedure: X-rays and CT scan Arthritis Procedure: Exercise Subacromial program; Procedure: Impingement Movement exercises Syndrome Rec 70 Adt Apr-08 Sep-11 University of Sen Nebraska http://ClinicalTrials.gov/show/NCT00670852 Comp 102 Adt Jan-08 Jun-11 Linkoeping Sen University http://ClinicalTrials.gov/show/NCT01037673 Procedure: Recurrent Shoulder Arthroscopic Bankart Dislocations repair; Procedure: ABR+ARIC Rec Procedure: Open Disorder of Tendon proximal biceps of Biceps tendon tenodesis with an EndoButton Biceps tenodesis + Osteoarthritis primary shoulder arthroplasty; primary shoulder arthroplasty alone Not yet Rec 10 Adt Comp 50 Adt Feb-06 Feb-11 Department of Sen Health (UK) Procedure: Open stabilization; Procedure: Arthroscopic stabilization Joint Instability; Active, Shoulder Dislocation NR 100 Child May-09 May-11 Tel-Aviv Adt Sourasky Medical Center N/K http://ClinicalTrials.gov/show/NCT00901797 Mar-11 West Penn http://ClinicalTrials.gov/show/NCT01317771 Allegheny Health System http://www.controlledtrials.com/ISRCTN71203361 194 Child Nov-01 Dec-10 University of http://ClinicalTrials.gov/show/NCT00251264 Adt Calgary; Alberta Sen Health Services; Calgary Orthopaedic Research and Education Fund; Canadian Orthopaedic Foundation 111 Reducing Shoulder Tip Pain Following Laparoscopic Surgery Phase III: RCT, safety/efficacy study NCT01135836 Procedure: Pulmonary recruitment maneuver; Procedure: Intraperitoneal normal saline; Procedure: Control group Electrothermal Arthroscopic Procedure: Capsulorrhaphy (ETAC) and Open Electrothermal Inferior Capsular Shift in Patients arthroscopic With Shoulder Instability capsulorrhaphy RCT, efficacy study (ETAC); Procedure: NCT00251160 Open inferior capsular shift (ICS) Other Acromio-clavicular Dislocation Type III - Conservative Treatment Versus Surgical Hook Plate Treatment RCT, efficacy study NCT01110304 Shoulder Pain; Laparoscopic Surgery Rec Shoulder Dislocation Comp Other: Conservative Acromio-clavicular treatment - brace; Joint Dislocation Device: Hook plate (Type III) by Synthes Rec 180 Adt Aug-09 Sep-10 Taipei Veterans http://ClinicalTrials.gov/show/NCT01135836 Sen General Hospital,Taiwan; FNational Yang only Ming University 58 Child Dec-99 Feb-10 University of http://ClinicalTrials.gov/show/NCT00251160 Adt Calgary; Sen Canadian Institutes of Health Research; The Arthritis Society, Canada; Smith and Nephew (formerly Oratec Interventions) 56 112 Adt May-07 Feb-14 Hopital de l'Enfant-Jesus http://ClinicalTrials.gov/show/NCT01110304 Rehabilitation and return to work after shoulder surgery: the Shoulder Intervention Project RCT ISRCTN55768749 The effect of cost information on patient outcomes RCT ISRCTN84082441 MRI Findings in Throwing Shoulders of Waterpolo Players Non-randomized, parallel assignment NCT00959543 Occupational case Shoulder surgery Active management with workplace oriented advice (+usual advice); Standardised physiotherapy with graded exercises (+ usual advice); Occupational case management with workplace oriented advice and standardised physiotherapy with graded exercises; usual training and advice No information Primary arthroscopic Comp regarding the cost of shoulder treatment; decompression Information regarding the cost of the surgery; Information regarding cost of the information specific to the study site Other: MRI Waterpolo Players; Comp Non Throwing Shoulders Miscellaneous observational studies Patient Benefit From the New Modular Shoulder Prosthesis PROMOS Prospective, cohort study NCT00925496 TESS Shoulder Arthroplasty Data Collection Prospective, cohort study NCT00751673 Primary or Secondary Omarthrosis of the Shoulder Joint Shoulder Replacement 400 Adt Nov-10 Oct-12 Danish Ramazzini Center (Denmark) 180 N/K Jul-10 45 Adt Jul-09 Oct-10 Cantonal Hospital of St. Gallen Monly http://www.controlledtrials.com/ISRCTN55768749 Jul-11 Imperial College http://www.controlledLondon (UK) trials.com/ISRCTN84082441 http://ClinicalTrials.gov/show/NCT00959543 Rec 240 Adt Jun-09 Dec-20 Smith & Nephew http://ClinicalTrials.gov/show/NCT00925496 Sen Orthopaedics AG Active, NR 600 Adt Jan-06 Oct-20 Biomet, Inc.; Sen Biomet France SARL 113 http://ClinicalTrials.gov/show/NCT00751673 Hospital for Special Surgery Shoulder Arthroplasty Cohort Cohort study NCT00527839 S.E.S Shoulder Arthroplasty Data Collection Prospective, cohort study NCT00754416 Functional and Radiographic Outcomes After Shoulder Surgery Cohort study NCT01405781 Comparison of Pain Relief After Non Stimulating Interscalene Catheter Placement vs Stimulating Catheter Placement in Total Shoulder Arthroplasty. Prospective study NCT01122732 Burden of Shoulder Disorders in Primary Health Care Prospective, cohort study NCT01300091 Assessing Cerebral Blood Flow Autoregulation During Surgery in the Head-up Position Prospective, case control study NCT01225185 Daptomycin With Rifampin for Treatment of Staphylococcal Prosthetic Joint Infection Prospective, cohort study NCT01144000 Shoulder Arthroplasty Shoulder Joint Arthroplasty Shoulder Pain; Osteoarthritis of Glenohumeral Joint; Reverse Total Shoulder Arthroplasty Pain; Shoulder; Arthroplasty Shoulder Pain; Shoulder Mobility Impairment Patients Undergoing Shoulder Surgery Rec 250 Adt Apr-07 Apr-17 Hospital for http://ClinicalTrials.gov/show/NCT00527839 Sen Special Surgery, New York Active, NR 100 Adt Mar-03 Sep-16 Biomet, Inc.; Sen Biomet France SARL http://ClinicalTrials.gov/show/NCT00754416 Invite 550 Adt May-11 May-15 University of Sen Utah http://ClinicalTrials.gov/show/NCT01405781 Rec 80 Adt Aug-10 Aug-12 University of Sen Chicago http://ClinicalTrials.gov/show/NCT01122732 Active, NR Rec Staphylococcal Not yet Infections; Rec Prosthesis; hip, knee and shoulder Prosthetic Joint Infection (PJI) 128 Child Oct-07 Aug-12 Central Finland http://ClinicalTrials.gov/show/NCT01300091 Adt Hospital District Sen 240 60 114 Adt Sen Jul-10 Jun-12 National Heart, http://ClinicalTrials.gov/show/NCT01225185 Lung, and Blood Institute (NHLBI); Anesthesia Patient Safety Foundation Adt Sep-10 Jun-11 Centre http://ClinicalTrials.gov/show/NCT01144000 Sen Hospitalier Universitaire Vaudois; University of Lausanne Hospitals; Kantonsspital Liestal; Schulthess Klinik Daptomycin With Rifampin for Treatment of Staphylococcal Prosthetic Joint Infection Prospective, cohort study NCT01144000 Staphylococcal Not yet Infections; Rec Prosthesis; hip, knee and shoulder Prosthetic Joint Infection (PJI) 60 Assessment of Weber Humeral Derotational Osteotomy Using CT Scan Prospective, cohort study NCT00358904 Validation of a Score for Shoulder Function Evaluation Based on Movement Analysis Prospective study NCT01281085 Hill Sachs Comp 20 Shoulder Pain Comp 16 115 Adt Sep-10 Jun-11 Centre http://ClinicalTrials.gov/show/NCT01144000 Sen Hospitalier Universitaire Vaudois; University of Lausanne Hospitals; Kantonsspital Liestal; Schulthess Klinik Child May-06 Apr-11 University of http://ClinicalTrials.gov/show/NCT00358904 Adt British Columbia Sen Adt Oct-10 Apr-11 Haute Ecole Sen Cantonale Vaudoise de Santé; Réseau d'études appliquées des pratiques de Santé de Réadapation (ré)insertion http://ClinicalTrials.gov/show/NCT01281085 A6. HAND & WRIST A6A: PAEDIATRICS Title Interventions Phases: trial design (control) CT ID Procedure A Comparison of Casting and Procedure: Volar Splinting in Pediatric Radial Buckle Splint; Procedure: Fractures Cast Phase II: RCT NCT01010347 Closed Reduction of Distal Procedure: Distal Forearm Fractures by Pediatric Forearm Fracture Emergency Medicine Physicians: Reduction A Prospective Study RCT, efficacy study NCT01101607 Miscellaneous observational studies Accuracy of common radiological methods to diagnose scapholunar dissociation: a prospective diagnostic efficacy study Prospective, cohort study ISRCTN57744239 The Natural History of Congenital Trigger Thumbs Prospective, case-only study NCT01424995 Conditions Recruit n Age Start (Grp) Date End Sponsors Date URL Distal Radial Buckle Fractures Comp 100 Child Dec-05 Apr-11 Washington University School of Medicine Pediatric Distal Forearm Fractures Comp 104 Child Apr-08 Apr-10 InMotion http://ClinicalTrials.gov/show/NCT01101607 Adt Orthopaedic Research Center; University of Tennessee Health Science Center; Le Bonheur Children's Medical Center; Campbell Clinic Wrist injury; Wrist pain; Traumatic scapholunar (SL) dissociation Comp 230 Congenital Trigger Thumb; Tenosynovitis Invite 100 Child Dec-10 Dec-15 University of Utah 116 Adt http://ClinicalTrials.gov/show/NCT01010347 Jan-09 Jan-11 Deutsche http://www.controlledArthrose-Hilfe trials.com/ISRCTN57744239 e.V. (Germany) http://ClinicalTrials.gov/show/NCT01424995 A6B: FRACTURE & INJURY Title Interventions Phases: trial design (control) CT ID Behavioural Effects of Motor Cognitive Training Behavioral: motor on Functional Loss After cognitive therapies Osteoporotic Wrist Fractures RCT, efficacy study NCT01394809 Device Use of Compression Glove to Prevent Complications After Distal Radius Fractures: a Randomized Controlled Trial RCT, efficacy study NCT01118715 Compression Gloves for Distal Radius Fracture RCT, safety/efficacy study NCT01518179 Conditions Osteoporotic Distal Radius Fracture Device: Compression Post-traumatic glove Carpal Tunnel Syndrome; Complex Regional Pain Syndrome; Edema Recruit n Age Start (Grp) Date Rec 36 Adt Aug-10 Aug-12 University of http://ClinicalTrials.gov/show/NCT01394809 Sen Stuttgart; German Federal FMinistry of only Education and Research Rec 460 Adt Apr-10 Apr-14 J&M Shuler Sen http://ClinicalTrials.gov/show/NCT01118715 Adt Mar-12 Mar-14 Clalit Health Sen Services; University of Haifa http://ClinicalTrials.gov/show/NCT01518179 Device: Made-toDistal Radius Not yet 120 Measure Fractures; Fracture Rec Compression Gloves of Lower End of Radius; Colles' Fracture; Smith's Fracture 2.4 mm Variable Angle LCP Two- Device: Variable Distal Radius Rec 74 Column Volar Distal Radius Angle Distal Radius Fractures Phase IV: Single group Plate ® (Surgery) assignment, efficacy study NCT01103297 Metaphyseal Distal Radius Device: - locking Metaphyseal Radius Rec 90 Fractures anterior plate Fractures (AO Type RCT, efficacy study A2, A3, C1 et C2) NCT01156766 Safety Study on a Wood-plastic Device: Omnicast Composite Cast Single group assignment, safety study NCT01340391 Distal Radius Fracture Invite 33 117 End Sponsors Date URL Adt Jun-10 Nov-12 AO Clinical http://ClinicalTrials.gov/show/NCT01103297 Sen Investigation and Documentation Adt Jun-10 Jun-12 University http://ClinicalTrials.gov/show/NCT01156766 Sen Hospital, ClermontFerrand; Stryker SA; Polyclinique du Parc Rambot Child Aug-09 Jun-11 Helsinki http://ClinicalTrials.gov/show/NCT01340391 Adt University Sen Central Hospital Fixation of Unstable Distal Radius Device: Micronail; Fractures Procedure: Volar Single group assignment, Plate Fixation efficacy study NCT00654615 Long Term Follow up of the DVR-A Device: ORIF with Locking Plate DVR-A locking plate Retrospective, cohort study NCT01122628 Dynasplint for Distal Radius Fracture Single group assignment, efficacy study NCT01032356 Drugs including biologics Fractures and Bisphosphonates: does osteoporosis treatment affect fracture healing? RCT ISRCTN62133820 Effect of treatment with L0006CP on the time of fracture-healing RCT (placebo) ISRCTN71678602 Efficacy of Baby Talcum in Prevention of Pruritus Assosiated With Cast Phase III: RCT, safety/efficacy study NCT01017315 SOLID-Effect of Risedronate Sodium at Distal Radius in Colle's Fracture. Phase IV: RCT, safety/efficacy study NCT00460733 Distal Radius Fractures Distal Radial Fractures Treated With a DVR-A Locking Plate Device: Wrist Distal Radius Extension Dynasplint Fracture Alendronic acid; placebo Distal radial fracture Rec 64 Adt May-08 Apr-11 Wake Forest Sen University; Wright Medical Technology http://ClinicalTrials.gov/show/NCT00654615 250 Child May-10 Dec-10 Norfolk and Adt Norwich Sen University Hospitals NHS Foundation Trust; De Puy; Global Diagnostics Not yet 50 Adt Jan-10 Jun-10 Dynasplint Rec Sen Systems, Inc. http://ClinicalTrials.gov/show/NCT01122628 Invite http://ClinicalTrials.gov/show/NCT01032356 Active 500 Adt Sep-11 Sep-13 University of http://www.controlledSen Edinburgh (UK) trials.com/ISRCTN62133820 L0006CP film-coated Wrist fracture tablets; placebo Comp 90 Adt Mar-11 Oct-11 Pierre Fabre Sen (France) http://www.controlledtrials.com/ISRCTN71678602 Drug: Baby talcum Invite 50 Child Jul-09 Oct-11 Prince of Adt Songkla Sen University http://ClinicalTrials.gov/show/NCT01017315 Comp 141 Child Mar-07 Sep-11 Sanofi-Aventis; Adt Procter and Sen Gamble http://ClinicalTrials.gov/show/NCT00460733 Fracture Distal Radius Drug: Risedronate Colles' Fracture sodium; Drug: Calcium & Vitamine D3 Fonly 118 Procedure Subcapital and Shaft Fractures of the 5. Metacarpal RCT, efficacy study NCT01242982 Procedure: Closed Fracture Rec reduction and fixation with 2 pins; Procedure: Reduction and Plaster of Paris Unstable Dorsally Displaced Procedure: open Fracture of the Distal Rec Fractures of the Distal Radius in reduction and Radius; Wrist the Elderly internal fixation with Fracture RCT a volar plate; NCT01268397 Procedure: closed reduction and plaster treatment Intraarticular Distal Radius Procedure: External Dorsally Displaced Rec Fractures, X-fix or Volar Fixation fixation; Procedure: Intraarticular Distal RCT, safety/efficacy study Volar plate Radius Fractures; NCT01035359 Age 50 - 74 for Females or 60-74 for Males; Low Energy Trauma Extraarticular Distal Radius Procedure: External Dorsally Displaced Rec Fractures, X-fix or Volar Fixation fixation; Procedure: Intraarticular Distal RCT, safety/efficacy study Volar plate Radius Fractures; NCT01034943 Age 50 - 74 for Females or 60-74 for Males; Low Energy Trauma Volar Locking Plate vs Fragment Procedure: Open Distal Radius Rec Specific Fixation in Wrist Fractures reduction and fixation Fractures RCT, efficacy study with TriMed NCT01311531 fragment-specific system; Procedure: Open reduction and fixation with TriMed volar locking plate External fixation or volar plating for Volar plating; Deviated distal Active treating deviated distal radius external fixation radius fracture fracture RCT ISRCTN09599740 200 Jan-11 Dec-14 St. Olavs Hospital; Norwegian University of Science and Technology Sen Dec-09 Dec-14 Danderyd Hospital http://ClinicalTrials.gov/show/NCT01242982 160 Adt Aug-09 Aug-14 Karolinska Sen Institutet http://ClinicalTrials.gov/show/NCT01035359 160 Adt Aug-09 Aug-14 Karolinska Sen Institutet http://ClinicalTrials.gov/show/NCT01034943 50 Adt Dec-10 May-14 Region Skane Sen http://ClinicalTrials.gov/show/NCT01311531 72 Adt Mar-12 Mar-14 Federal http://www.controlledSen University of São trials.com/ISRCTN09599740 Paulo (Brazil) 80 119 Adt http://ClinicalTrials.gov/show/NCT01268397 Assessing Volar Locking Plates in Procedure: Surgical Distal Radius Patients Under 65 With a Distal Repair of Distal Fracture Radius Fracture Radius Fracture RCT NCT01333371 Comparison of Three Fixation Techniques for Displaced Distal Radius Fractures Phase III: RCT, efficacy study NCT00524719 Procedure: Open Distal Radius Reduction and Fractures Internal Fixation; Procedure: NonSpanning External Fixation; Procedure: Closed Reduction with Percutaneous Fixation Unstable Fractures of the Distal Procedure: Volar Distal Radius Radius: Trial of Volar Plate Versus plate; Procedure: Fractures Dorsal Nail Plate Fixation Dorsal nail plate RCT, efficacy study NCT00848263 Comparison of surgical procedures K-wire Fixation; Volar Dorsally displaced for patients with a fracture of the locking plate fracture of the distal wrist radius RCT ISRCTN31379280 Functional Outcome Following Procedure: Kirschner Distal Radius Fracture of the Distal Radius wire fixation; Fractures Prospective, cohort study Procedure: Volar NCT01435070 Locking Plate fixation Hyperbaric Oxygen Therapy in Distal Radius Fractures: Can it Shorten Recovery Time and Increase Fracture Healing? RCT, efficacy study NCT01365780 Procedure: Hyperbaric Oxygen Therapy Hyperbaric Oxygen Therapy; Recovery Time; Contrast Media; Sonography Not yet Rec 64 Rec 324 Rec 120 Adt Feb-09 Dec-13 Sykehuset Asker http://ClinicalTrials.gov/show/NCT00848263 Sen og Baerum Active 390 Adt Sen Rec 50 Adt Jan-11 Oct-13 University of Sen Warwick; University Hospitals Coventry and Warwickshire NHS Trust; DePuy International Adt Jun-11 May-13 RWTH Aachen Sen University Not yet 100 Rec 120 Adt Apr-11 Mar-14 Hand and Upper http://ClinicalTrials.gov/show/NCT01333371 Limb Clinic, Canada; Canadian Orthopaedic Foundation Adt Jan-07 Dec-13 McGill University http://ClinicalTrials.gov/show/NCT00524719 Sen Health Center; Orthopaedic Trauma Association Jul-10 Dec-13 University of Warwick (UK) http://www.controlledtrials.com/ISRCTN31379280 http://ClinicalTrials.gov/show/NCT01435070 http://ClinicalTrials.gov/show/NCT01365780 Volar Locking Plate Versus External Fixator/Cast Fixation for the Treatment of Distal Radius Fractures RCT, efficacy study NCT00809861 Colles Fracture Brace prospective randomised Study RCT ISRCTN45883421 CoNCReTe-trial: Colles Fractures, Determining the Norm in Closed Reduction Techniques RCT, safety/efficacy study; NCT00631267 Outcome Study of Complex Distal Radius Fractures Phase IV: Case-only study NCT00160810 Procedure: volar Distal Radius locking plating; Fractures Procedure: external immobilisation Rec 60 Adt Aug-08 Sep-12 Mackay Base http://ClinicalTrials.gov/show/NCT00809861 Sen Hospital; James Cook University, Queensland, Australia 340 Adt Nov-09 May-12 NHS Grampian Sen (UK) Plaster of paris (POP) cast; Brace; Surgery. Colles fracture Active Procedure: Manual Manipulation; Procedure: Finger Trap Traction Colles' Fracture Rec 300 Child Jul-08 May-12 Rijnstate Adt Hospital Sen http://ClinicalTrials.gov/show/NCT00631267 Rec 120 Adt Apr-01 Apr-12 University of Sen Florida http://ClinicalTrials.gov/show/NCT00160810 Term 6 Adt Feb-11 Jan-12 Mayo Clinic Sen http://ClinicalTrials.gov/show/NCT01293227 Comp 68 Adt Oct-10 Oct-11 Barnsley http://www.controlledSen Hospital NHS trials.com/ISRCTN08332539 Foundation Trust (UK) Procedure: ORIF All Distal Radius with a Volar Fixed Fractures Angled Plate; Procedure: ORIF with Distal Radius Volar (DRV) Plate; Procedure: External Fixation WRx Distal Radius Wrist Fracture Procedure: Surgical Wrist Fracture Study treatment of distal RCT, efficacy study radius fractures NCT01293227 Ultrasound guided supraclavicular Intravenous regional Closed fracture of brachial plexus block versus anaesthesia; the distal third of the intravenous regional anaesthesia Supraclavicular radius for the manipulation of fractures of brachial plexus block the distal radius RCT, efficacy study ISRCTN08332539 Osteoporosis and Colles Fracture Procedure: DEXA Previous or Actual Retrospective scan Colles Fracture NCT00225004 Term 5000 Adt Sen Fonly 121 Jul-04 Aug-11 Northern Orthopaedic Division, Denmark http://www.controlledtrials.com/ISRCTN45883421 http://ClinicalTrials.gov/show/NCT00225004 Exploration of Wrist Soft Tissue Injuries Associated With Wrist Fractures Single group assignment NCT01145716 Conservative Versus Operative Treatment of Displaced Neck Fractures of the Fifth Metacarpal RCT NCT00704002 Procedure: Triangular Arthroscopy, surgery Fibrocartilage Complex Injuries Procedure: antegrade intramedullary splinting; Procedure: conservative treatment A Randomized Controlled Trial of Procedure: the Treatment of Mallet Fractures Biodegradable RCT, efficacy study Meniscus Arrow®; NCT01232426 Device: Mallet splint Comparison of Two Methods for Procedure: Treatment of Colles´s Fracture Osteosynthesis RCT NCT00609479 Range of Motion and Patients With Procedure: Physical Distal Radius Fractures therapy; Procedure: RCT, efficacy study Physical Therapy NCT00816998 Other Early Motion After Volar Fixation for Distal Radius Fractures RCT, safety/efficacy study NCT00955734 Vestibular Rehabilitation for Patients With Fall-related Wrist Fractures RCT, efficacy study NCT00988572 Contribution of ESAOTE™ Low Field MRI for Diagnosis of Scaphoid Fractures Single group assignment, efficacy study NCT01235806 Comp 20 Adt Aug-09 May-11 Linkoeping University http://ClinicalTrials.gov/show/NCT01145716 Fifth Metacarpal Neck Fracture Rec 80 Adt Dec-06 Dec-10 Heinrich-Heine Sen University, Duesseldorf http://ClinicalTrials.gov/show/NCT00704002 Mallet Fracture Active, NR 84 Adt Sen Distal Radius Fracture; Colle´s Fracture Comp 60 Adt Jan-08 Feb-10 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT00609479 Radius Fractures Comp 39 Adt Oct-06 Feb-10 Mayo Clinic; Sen DePuy Orthopaedics http://ClinicalTrials.gov/show/NCT00816998 Invite 80 Adt Jun-09 Jun-12 Washington http://ClinicalTrials.gov/show/NCT00955734 Sen University School of Medicine Adt Mar-09 Mar-12 Lund University http://ClinicalTrials.gov/show/NCT00988572 Sen Other: Early motion; Radius Fracture Other: Immobilization Other: Vestibular rehabilitation Wrist Fractures; Dizziness Rec 100 Radiation: MRI Scaphoid Bone Fracture Suspicion Rec 50 122 N/K Oct-10 Conmed Linvatec Benelux http://ClinicalTrials.gov/show/NCT01232426 Adt Mar-09 Jan-12 Centre http://ClinicalTrials.gov/show/NCT01235806 Sen Hospitalier Universitaire de Nice Mirror Therapy and Hand Rehabilitation RCT NCT01503762 Other: Mirror therapy; Other: Classical rehabilitation techniques Miscellaneous observational studies Distal Radius Fracture Prospective Database 50-80 Years Old Prospective, cohort study NCT01497080 Volar Locked Plating Versus Bridging External Fixation Prospective, case control study NCT01062997 Swelling or Malrotation of Metacarpal Shaft Fractures in the Evaluation of Rotational Deformity Prospective, cohort study NCT00934869 The Treatment and Intra-operative Imaging of Scaphoid Fracture Reduction and Fixation Prospective, cohort study NCT01249898 Comparison of Occupational Therapy and Home Exercises for Adults With Operatively Treated Distal Radius Fractures Prospective, cohort study NCT00438750 The Influence of Local Bone Status on Complications After Surgical Treatment of Distal Radius Fractures Phase IV: Prospective, cohort study NCT01144208 Hand Fractures Comp 23 Radius Fracture Distal Not yet 195 Rec Adt Jan-09 Dec-11 Ahvaz Jundishapur University of Medical Sciences Adt Jan-12 Jan-15 Lawson Health Sen Research Institute http://ClinicalTrials.gov/show/NCT01503762 http://ClinicalTrials.gov/show/NCT01497080 Distal Radius Fracture Rec 140 Metacarpal Shaft Fractures Rec N/K Scaphoid Fractures Rec N/K Adt Sen Distal Radius Fractures Active, NR 60 Adt Aug-06 Feb-11 Massachusetts http://ClinicalTrials.gov/show/NCT00438750 Sen General Hospital Distal Radius Fractures; Poor Bone Quality; Treatment Complications Comp 244 Adt Feb-07 Apr-10 AO Clinical http://ClinicalTrials.gov/show/NCT01144208 Sen Investigation and Documentation 123 Adt Sep-09 Mar-14 University http://ClinicalTrials.gov/show/NCT01062997 Sen Hospital, Akershus; University of Oslo; Haukeland University Hospital Adt Aug-09 Dec-11 Hadassah http://ClinicalTrials.gov/show/NCT00934869 Sen Medical Organization N/K Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT01249898 A6C: OTHER Title Phases: trial design (control) CT ID Behavioural Early Motion Following Carpal Tunnel Release RCT, efficacy study NCT00845325 Device Ascension® MCP Post-Approval Study Single group assignment NCT01398735 Interventions Conditions Behavioral: early motion; Behavioral: Control group Carpal Tunnel Syndrome Recruit Rec Device: Ascension Rheumatoid Arthritis; Rec MCP Finger Implant Systemic Lupus Erythematosus; Osteoarthritis; Posttraumatic Arthritis Dupuytren's Disease and Device: Intervention - Dupuytren Rec Extracorporeal Shockwave ESWT Storz Duolith Contracture Therapy (DupuyShock-2010) high energy; Device: Phase II: RCT, efficacy study CONTROL SHAMNCT01184586 ESWT Storz Duolith [0.01mJ/mm2] Evaluation of the MANOS Carpal Device: MANOS Carpal Tunnel Invite Tunnel Release System in Patients CTR™ Syndrome With Carpal Tunnel Syndrome Single group assignment NCT01450735 IMS-treatment and Canalis Carpi Device: Needle in Carpal Tunnel Comp Syndrome acupuncture point Syndrome RCT, bio-equivalence study Li11; Device: IMS of NCT01102868 the musculus pronator teres Using HandTutor With Traumatic Device: HandTutor Hand Injuries. Rec Hand Injuries: Characterizing the System System Non-randomized, parallel assignment NCT01210833 n Age Start (Grp) Date End Sponsors Date 100 Child Dec-08 Dec-11 University of Adt MissouriSen Columbia URL http://ClinicalTrials.gov/show/NCT00845325 100 Adt Feb-02 Dec-13 Ascension http://ClinicalTrials.gov/show/NCT01398735 Sen Orthopedics, Inc. 60 Adt Nov-11 Dec-12 Hannover Sen Medical School http://ClinicalTrials.gov/show/NCT01184586 100 Adt Oct-11 Sep-12 Thayer Sen Intellectual Property, Inc. http://ClinicalTrials.gov/show/NCT01450735 75 Adt Apr-09 Jan-12 UNIFOB A/S Sen http://ClinicalTrials.gov/show/NCT01102868 40 Adult Oct-10 Dec-11 Meir Medical Center http://ClinicalTrials.gov/show/NCT01210833 124 Adaprev in Digital Flexor Tendon Device: Adaprev Tendon Injuries Repair RCT, safety/efficacy study NCT01014494 Prospective clinical trial comparing C-Trac™ splint; Carpal tunnel C-Trac™ splint with conventional Conventional resting syndrome resting splint for treatment of splint carpal tunnel syndrome Effect of orthoses in hand Prefabricated Osteoarthritis of the osteoarthritis orthosis + Exercise; carpometacarpal RCT Exercise only joint ISRCTN40357804 An RSA and DEXA Study on Device: Avanta (PIP Osteoarthritis Migration of Proximal joint implant with a Interphalangeal (PIP) Joint titanium porous Prostheses of the Hand coating) RCT, safety/efficacy study NCT00175188 Splinting after Contracture Release Surgery for Dupuytren’s for Dupuytren's contracture release + Contracture RCT usual post-operative ISRCT57079614 hand therapy ± static night splint Rec 44 Adt Sep-09 Dec-11 Renovo Sen Comp 50 Adt Comp 60 Adt Nov-08 Dec-10 Diakonhjemmet http://www.controlledSen Hospital trials.com/ISRCTN40357804 (Norway) Comp 30 Adt Jun-04 Oct-10 University of http://ClinicalTrials.gov/show/NCT00175188 Sen Aarhus; Aarhus University Hospital; Biomet, Inc.; Avanta Comp 128 Adt Oct-07 Apr-10 University of http://www.controlledSen East Anglia (UK) trials.com/ISRCTN57079614 Drugs including biologics Post Approval Commitment Study Drug: Xiapex; Dupuytren's Not yet Phase IV: Prospective study Procedure: surgery Contracture Rec NCT01444729 Assessment of Efficacy and Safety Drug: co.don Large Articular Rec of 3 Different Doses of co.Don chondrosphere® Cartilage Lesions of Chondrosphere to Treat Large the Femoral; Cartilage Defects Condyle, Trochlea, Phase II: RCT, safety/efficacy Tibia or Retropatellar study NCT01225575 Injectable Collagenase and Drug: Xiapex; Dupuytrens Rec Percutaneous Needle Fasciotomy Procedure: Contracture for Dupuytren's Contracture Percutaneous needle RCT, safety/efficacy study fasciotomy NCT01538017 http://ClinicalTrials.gov/show/NCT01014494 Jun-06 Jun-11 Derby Hospitals http://www.controlledNHS Foundation trials.com/ISRCTN26618585 Trust (UK) 0 Adt Jan-12 Mar-18 Pfizer Sen http://ClinicalTrials.gov/show/NCT01444729 75 Adt http://ClinicalTrials.gov/show/NCT01225575 50 Adt Feb-12 Jan-15 Jeppe Lange, Sen MD 125 Oct-10 Jul-16 co.don AG http://ClinicalTrials.gov/show/NCT01538017 Botulism Toxin Injection as a Treatment for Arthritis of the Basal Thumb Joint Phase IV: RCT, safety/efficacy study NCT01045694 Drug: Botulinum Toxin Type A; Drug: Triamcinolone Acetonide; Drug: Lidocaine Basilar Joint Rec 45 Arthritis; Basal Thumb Joint Arthritis; Trapeziometacarpal Arthritis; Carpometacarpal Arthritis Biological: XIAFLEX / Dupuytren's Disease Not yet 100 XIAPEX Rec Retreatment of Recurrent Dupuytren's Contractures Phase IV: Single group assignment, safety/efficacy study NCT01498640 Study of PXL01 Versus Placebo to Drug: PXL01; Drug: Surgical Adhesions Inhibit Adhesion Formation After Placebo Flexor Tendon Surgery Phase II: RCT, safety/efficacy study NCT01022242 Administration of Two Injections for Biological: AA4500 Dupuytren's Multiple Dupuytren's Contractures collagenase Contracture Phase III: Single group clostridium assignment, safety/efficacy histolyticum study NCT01407068 Steroid Injection Treatment of Drug: Carpal Tunnel Carpal Tunnel Syndrome Methylprednisolone Syndrome Phase II/III: RCT, safety/efficacy 40 mg; Drug: study Methylprednisolone NCT00806871 80 mg; Drug: Sodium chloride The effect of dexmedetomidine in Levobupivacaine + Forearm and hand addition to local anaesthetic on the dexmedetomidine + surgery patients block of nerves in the arm isotonic sodium RCT chloride; ISRCTN67622282 Levobupivacaine + isotonic sodium chloride Rec Adt Mar-11 Nov-13 University of Sen MissouriColumbia http://ClinicalTrials.gov/show/NCT01045694 Adt Mar-12 Sep-13 Auxilium http://ClinicalTrials.gov/show/NCT01498640 Sen Pharmaceuticals 138 Child Dec-09 Jun-12 PharmaSurgics http://ClinicalTrials.gov/show/NCT01022242 Adt AB Active, NR 60 Adt Sep-11 Apr-12 Auxilium http://ClinicalTrials.gov/show/NCT01407068 Sen Pharmaceuticals Rec 120 Adt Nov-08 Mar-12 Region Skane Sen http://ClinicalTrials.gov/show/NCT00806871 Comp 64 Adt Nov-11 Feb-12 Cumhuriyet Sen University (Turkey) http://www.controlledtrials.com/ISRCTN67622282 126 MRI Results in Dupuytren's Biological: XIAFLEX Dupuytren's Disease Active, Contracture Before and After NR Injection With Xiaflex Phase IV: Single group assignment NCT01450397 Study Comparing One Versus Two Drug: One cortisone Stenosing Rec Cortisone Injections for Trigger injection; Drug: Two Tenosynovitis; Finger cortisone Injections Trigger Finger Parallel assignment, efficacy study NCT00951236 ED95 bupivacaine and Bupivacaine for Routine hand, Comp supraclavicular block supraclavicular forearm or upper Single group assignment, brachial plexus block limb surgery safety/efficacy study ISRCTN63230740 A Study of Hyaluronan for the Drug: Synvisc (Hylan Osteoarthritis Rec Treatment of Osteoarthritis in the G-F20; hyaluronan Thumb injection); Drug: Phase III: RCT Bupivicaine (local NCT00398866 anesthesia injection); Drug: Kenalog (triamcinolone; corticosteroid injection) Procedure Hand Transplantation for the Procedure: Hand Amputation; Reconstruction of Below the Elbow transplantation Transplantation Amputations Single group assignment, safety/efficacy study NCT00778856 Follow-up of Patients After 4-row Procedure: Wrist Surgery Arthrodesis or Proximal Row Anamnesis and Carpectomy clinical examination Single group assignment, efficacy study NCT00284310 5 Adt Mar-11 Feb-12 Scott Wolfe; http://ClinicalTrials.gov/show/NCT01450397 Sen Auxilium Pharmaceuticals , Inc 392 Adt May-09 Nov-11 Rothman Sen Institute Orthopaedics http://ClinicalTrials.gov/show/NCT00951236 40 Adt Oct-09 Oct-10 University of Sen Leeds (UK) http://www.controlledtrials.com/ISRCTN63230740 213 Adt Aug-06 Aug-10 Hospital for http://ClinicalTrials.gov/show/NCT00398866 Sen Special Surgery, New York; Genzyme Rec 5 Adt Sep-08 Dec-22 Emory University http://ClinicalTrials.gov/show/NCT00778856 Rec 40 Adt Oct-05 Dec-20 University http://ClinicalTrials.gov/show/NCT00284310 Sen Hospital, Ghent 127 Human Upper Extremity Allotransplantation Single group assignment, safety/efficacy study NCT00722280 Allograft Meniscal Arthroplasty for the Treatment of Basal Joint Arthritis of the Thumb Prospective, cohort study NCT01542515 Allogeneic Hand Transplantation Composite Tissue Allotransplantation Phase II: Single group assignment, efficacy study NCT00711373 Procedure: Hand Transplantation Hand Transplantation for Treatment of Dominant Hand or Bilateral Hand Amputees Single group assignment, safety/efficacy study NCT01293214 Open Surgery Versus Corticosteroid Injections in Treatment of Trigger Finger RCT, efficacy study NCT01486420 Suture Fixation System Versus Tendonous Reconstruction in Carpometacarpal (CMC) Arthroplasty RCT, efficacy study NCT01121874 Procedure: Hand transplantation Procedure: Corticosteroid injections; Procedure: Open surgery Procedure: Ligament reconstruction with suture fixation system; Procedure: Ligament Reconstruction with Tendon Interposition Amputation, Traumatic Invite 300 Adt Dec-08 Jan-18 University of Pittsburgh http://ClinicalTrials.gov/show/NCT00722280 Active, NR 20 Adt Mar-09 Sep-16 William Sen Beaumont Hospitals; LifeNet Health http://ClinicalTrials.gov/show/NCT01542515 Rec 10 Adt Upper Extremity Amputation; Hand Amputation Rec 10 Trigger Finger Rec 166 Adt Jan-12 Jan-15 Jeppe Lange, Sen MD http://ClinicalTrials.gov/show/NCT01486420 Thumb Carpometacarpal Arthritis Rec 60 Adt Apr-10 Apr-14 J&M Shuler Sen http://ClinicalTrials.gov/show/NCT01121874 Procedure: Meniscal Arthritis allograft arthroplasty of the carpometacarpal joint of the thumb Procedure: Upper Extremity Allogeneic hand Injuries; Amputation transplantation 128 Jun-98 Jun-15 Christina L. http://ClinicalTrials.gov/show/NCT00711373 Kaufman PhD; Jewish Hospital and St. Mary's Healthcare; Kleinert, Kutz and Associates; University of Louisville; U.S. Army Medical Research and Materiel Command; Department of Defense Adt Feb-10 Feb-15 Brigham and http://ClinicalTrials.gov/show/NCT01293214 Women's Hospital The Effects of a Stainless Steel Procedure: Stainless Zone 2 Flexor Not yet 24 Adt Suture MGH Flexor Tendon Repair steel suture; Tendon Lacerations Rec Sen Coupled With Early Aggressive Procedure: of the Hand Range of Motion Rehabilitation: a Polypropylene Randomized Controlled Trial suture; Behavioral: Phase II: RCT, safety/efficacy Aggressive early study active range of NCT01344980 motion rehabilitation; Behavioral: Early active range of motion rehabilitation Prevention of Phantom Limb and Procedure: Amputation; Active, 18 Adt Stump Pain Using Ambulatory perineural ropivicaine Phantom Limb Pain; NR Sen Continuous Peripheral Nerve Stump Pain Blocks Phase IV: RCT, safety/efficacy study NCT00771862 Axillary Plexus Block in a High Procedure: Axillary Nerve Block; Invite 45 Adt Resolution MRI plexus block and Magnetic Sen Phase II: RCT, efficacy MRI Resonance Imaging studyNCT01033006 Vascularized Versus NonProcedure: Scaphoid NonRec 40 Adt Vascularized Bone Grafts in Vascularized Bone Unions Sen Treating Proximal Pole Scaphoid Graft; Procedure: Non Unions Non-Vascularized RCT, efficacy study Bone Graft NCT01419808 PRCT: Comparing Ligament Procedure: LRTI; Joint Disease Rec 130 Adt Reconstruction and Tendon Procedure: Sen Interposition (LRTI) With a Joint Ascension PyroDisk Spacer for Trapeziometacarpal (TMC) Osteoarthritis (OA) (TMC/PyroDisk Study) RCT, efficacy study NCT00671333 Traumatic Ulnar Translocation of Procedure: Surgery Traumatic Ulnar Comp 10 Child the Carpus or immobilization Translocation of the Adt Retrospective, case-only study Carpus Sen NCT01258166 129 Jun-11 Jun-13 University of Manitoba http://ClinicalTrials.gov/show/NCT01344980 Oct-08 Dec-12 University of http://ClinicalTrials.gov/show/NCT00771862 California, San Diego; National Institute of General Medical Sciences (NIGMS) Jan-09 Oct-12 Diakonhjemmet http://ClinicalTrials.gov/show/NCT01033006 Hospital; Oslo University Hospital Sep-07 Jul-12 Hand and Upper http://ClinicalTrials.gov/show/NCT01419808 Limb Clinic, Canada Apr-08 Apr-12 Simon Fraser Orthopaedic Fund http://ClinicalTrials.gov/show/NCT00671333 Jan-05 Jan-12 Northwestern University http://ClinicalTrials.gov/show/NCT01258166 Ambulatory Continuous Peripheral Procedure: Nerve Blocks for Treatment of perineural Post-Amputation Phantom Limb ropivacaine and Stump Pain RCT, efficacy study NCT00667264 Proximal Interphalangeal Joint Arthroplasty Using a Graft From the Capitate Single group assignment, safety study NCT01479738 Hypoalgesic and motor effects of Kaltenborn mobilization on elderly patients with secondary thumb carpometacarpal osteoarthritis RCT ISRCTN06361999 Surgical Versus Conservative Treatment of Acute Mallet Fingers; a Randomised Controlled Trial RCT, efficacy study NCT01016197 Post-operative Mobilization for Carpal Tunnel Syndrome RCT NCT00435149 Comp 7 Procedure: Capitate Recurrent bone grafting Dislocation of Hand Comp 18 Kaltenborn’s mobilization technique; Placebo Comp 26 Sen May-11 Jun-11 Azienda http://www.controlledSanitaria Locale trials.com/ISRCTN06361999 (ASL) 3 (Italy) Procedure: extensor Finger Injury tendon repair Not yet Rec 50 Child Jan-10 Jun-11 Mid Cheshire http://ClinicalTrials.gov/show/NCT01016197 Adt Hospitals NHS Sen Foundation Trust Procedure: Carpal Carpal Tunnel tunnel release Syndrome surgery; Procedure: Carpal tunnel release surgery Percutaneous needle Dupuytren’s disease fasciotomy; limited fasciectomy Comp 100 Adt Dec-06 Feb-11 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00435149 Comp 120 N/K Aug-02 Jan-11 University Medical Centre Groningen (Netherlands) http://www.controlledtrials.com/ISRCTN58554745 Invite 60 Percutaneous needle fasciotomy versus limited fasciectomy in Dupuytren's disease RCT ISRCTN58554745 Carpal Tunnel Syndrome Release Procedure: Limited Using PSU Retractor incision using PSU Phase III: RCT, safety/efficacy retractor study NCT01017471 Amputation; Phantom Limb; Stump Pain Carpometacarpal osteoarthritis Carpal Tunnel Syndrome 130 Adt Oct-08 Dec-11 University of http://ClinicalTrials.gov/show/NCT00667264 Sen California, San Diego; Summit Medical; National Institute of General Medical Sciences Adt Jan-05 Oct-11 The Second http://ClinicalTrials.gov/show/NCT01479738 Hospital of Qinhuangdao Child Sep-09 Dec-10 Prince of Adt Songkla Sen University http://ClinicalTrials.gov/show/NCT01017471 PRCT: Comparing Two Procedures for Ulno-Carpal Abutment Syndrome. RCT, efficacy study NCT00564980 Medial Versus Lateral Approach in Ultrasound (US)-Guided Supraclavicular Block RCT, efficacy study NCT00992810 Computer Assisted Planing of Corrective Osteotomy for Distal Radius Malunion RCT NCT01193010 Other Postoperative Rehabilitation Following Trapeziectomy and Ligament Reconstruction Tendon Interposition RCT, safety/efficacy study NCT01425034 Long-term Observational Evaluation of Subjects Treated With AA4500 in Studies AUX-CC854, AUX-CC-856, AUX-CC857/AUX-CC-858 and AUX-CC859 Prospective, cohort study NCT00954746 Diagnostic Accuracy of Direct MR Arthrography Of The Wrist At 1.5, 3.0 And 7.0T Prospective, case-only study NCT01012271 The Occlusive Dressing RCT, efficacy study NCT01002638 Procedure: Wafer Joint Disease Procedure; Procedure: Ulnar shortening osteotomy Procedure: Lateral- Hand or Arm to-Medial Approach; Surgery Procedure: Media-toLateral Approach Term 3 Child Jul-07 Dec-10 Simon Fraser Adt Orthopaedic Sen Fund Rec 78 Adt Aug-09 Sep-10 University Health http://ClinicalTrials.gov/show/NCT00992810 Sen Network, Toronto Procedure: Computer-Assisted Surgical Planning; Procedure: distal radius osteotomy Rec 40 Adt Aug-10 Aug-10 Massachusetts Sen General Hospital; AO foundation http://ClinicalTrials.gov/show/NCT01193010 Other: casts for the Osteoarthrosis of the Invite thumb; Other: Motion Carpometacarpal group Joint of the Thumb 210 Adt Sep-11 Sep-17 University of Sen Utah http://ClinicalTrials.gov/show/NCT01425034 Other: No Intervention Advanced Dupuytren's Disease Invite 600 Adt Sen Other: MRI Wrist Injuries Not yet Rec 70 Adt Oct-10 Dec-12 University of Sen Zurich http://ClinicalTrials.gov/show/NCT01012271 Rec 100 Adt Dec-09 May-12 University Sen Hospital, Strasbourg, France http://ClinicalTrials.gov/show/NCT01002638 Extraarticular Distal Radius Malunion Other: Fingertips Traumatic TEGADERM®; Amputations Procedure: Surgery 131 http://ClinicalTrials.gov/show/NCT00564980 Jul-09 Mar-13 Auxilium http://ClinicalTrials.gov/show/NCT00954746 Pharmaceuticals Determining the Minimum Effective Other: Bupivacaine Volume of Local Anesthetic for 0,5% Ultrasound-guided Axillary Brachial Plexus Block Single group assignment, efficacy study NCT01421914 Corticosteroid Injection as a Other: Corticosteroid Predictor of Outcome in Carpal Injection- 1ml of Tunnel Release Betamethasone and Prospective, cohort study 1 ml of 1% Lidocaine NCT00655915 The Role of Antibiotics After Other: No Surgical Treatment of Simple Hand intervention Infections: A Prospective Study Prospective, case control study NCT01429571 Length of Post Operative Dressing Other: extended After Carpal Tunnel Release postoperative Phase IV: RCT, efficacy study dressing; Other: NCT01310218 short postoperative dressing Miscellaneous observational studies Basal Joint Arthritis Prospective Prospective, cohort study NCT01376024 The Safety of Hand Surgery in the Anticoagulated Patient Prospective, case control study NCT00954928 Carpal Tunnel Release in Diabetic Patients Prospective, case control study NCT01201109 Axillary Brachial Plexus Block Active, NR 25 Adt Dec-10 Aug-11 Federal University of São Paulo http://ClinicalTrials.gov/show/NCT01421914 Carpal Tunnel Syndrome Term 200 Adt Dec-07 Mar-11 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00655915 Hand Infections Comp 90 Adt Aug-09 Dec-10 BG Trauma Sen Center Tuebingen http://ClinicalTrials.gov/show/NCT01429571 Carpal Tunnel Syndrome Comp 96 Adt May-09 Nov-10 University of Sen Connecticut Health Center http://ClinicalTrials.gov/show/NCT01310218 Rec 500 Adt Sen Invite 200 Adt Sen Carpal Tunnel Invite Syndrome; Diabetes; Nerve Entrapment 66 Adt Sen Osteoarthritis of the Basal Joint of the Thumb Hand Surgery 132 Jul-06 Sep-12 Columbia http://ClinicalTrials.gov/show/NCT01376024 University; Arthritis Foundation; American Society for Surgery of the Hand Jun-09 Jun-12 Washington http://ClinicalTrials.gov/show/NCT00954928 University School of Medicine Nov-10 Dec-11 Skane University http://ClinicalTrials.gov/show/NCT01201109 Hospital Medical Review: Hand Surgery After Local Block Versus Nonblock Retrospective, case control study NCT01110759 Health-Related Quality of Life in Patients With Dupuytren's Disease Phase I: Prospective, cohort study NCT00468949 Orthopaedic Hand Service Data Repository Cohort study NCT01393262 Splinting for Dupuytren's Contracture Release Prospective, cohort study NCT00575458 Biomechanical Evaluation of Wrist Ligament Injuries: Diagnostic Tool to Detect Wrist Instability Prospective, case-only study NCT00657072 Carpal Tunnel Syndrome Active, NR 200 Dupuytren's Contracture Comp 51 Non-traumatic and Traumatic Health Issues Rec Adt Aug-09 Jul-11 Cedars-Sinai Sen Medical Center http://ClinicalTrials.gov/show/NCT01110759 Adt May-07 Jul-11 Hamilton Health http://ClinicalTrials.gov/show/NCT00468949 Sen Sciences Corporation; McMaster University 2000 Adt Nov-09 Jul-11 Massachusetts http://ClinicalTrials.gov/show/NCT01393262 Sen General Hospital Dupuytren's Disease Comp 60 Adt Jun-05 Jun-10 Massachusetts http://ClinicalTrials.gov/show/NCT00575458 Sen General Hospital Scapholunate Invite Interosseous Ligament; Torn Wrist Ligaments 50 Child May-03 May-10 State University http://ClinicalTrials.gov/show/NCT00657072 Adt of New York Upstate Medical University; National Institutes of Health 133 A7. UPPER LIMB (including elbow) A7A: PAEDIATRICS Title Phases: trial design (control) CT ID Drugs including biologics The Post-Operative Pain Management of Pediatric Supracondylar Elbow Fractures RCT, efficacy study NCT01328782 Interventions Conditions Drug: Oxycodone Elbow Fracture with Acetaminophen; Drug: Bupivacaine 0.25%; Drug: Ropivacaine 0.20% Procedure Comparison of Tendon Transfer, Botox Injections and Ongoing Treatment in Hemiplegic Cerebral Palsy RCT, efficacy study NCT00250081 Procedure: Upper Cerebral Palsy Extremity Tendon transfer; Procedure: Botulinum Toxin injections in Upper Extremity; Procedure: Regularly ongoing therapy Treatment of Type I Supracondylar Procedure: Cast; Type I Fractures of the Humerus Procedure: Splint; Supracondylar RCT, safety/efficacy study Procedure: Tape Fracture of the NCT00904137 Humerus Nurse Reduction of Pulled Elbow Procedure: Radial Head RCT, safety/efficacy study Reduction of Radial Subluxation NCT00993954 Head Subluxation Other Effect of Occupational Therapy on Other: Occupational Supracondylar the Function and Mobility of Elbow therapy Humerus Fracture Fractures RCT, efficacy study NCT00871793 Recruit Active, NR n Age Start (Grp) Date End Sponsors Date URL 124 Child Jun-08 Jun-11 Children's http://ClinicalTrials.gov/show/NCT01328782 Hospital Colorad Rec 78 Child Feb-05 Dec-12 Shriners Hospitals for Children Rec 87 Child May-09 Feb-12 University of http://ClinicalTrials.gov/show/NCT00904137 British Columbia Rec 224 Child Oct-09 Oct-11 Children's http://ClinicalTrials.gov/show/NCT00993954 Hospital of Eastern Ontario; Ontario Ministry of Health and Long Term Care Rec 128 Child Mar-09 Sep-12 Seattle Children's Hospital 134 http://ClinicalTrials.gov/show/NCT00250081 http://ClinicalTrials.gov/show/NCT00871793 Randomized Trial of Casting Techniques for Displaced Forearm Fractures RCT, efficacy study NCT00823823 Self Cast Removal at the Child's Home RCT ISRCTN55089523 Other: Bivalved cast; Displaced Forearm Other: Fractures Circumferential cast Active, NR 224 Child Jan-09 Dec-11 Children's http://ClinicalTrials.gov/show/NCT00823823 Hospital Boston Traditional plaster of Upper limb fractures Paris or fibreglass in children rigid cast + fracture clinic for removal; Home-removable flexible cast taken off at home by the parent/carer. Comp 460 Child May08 Mar-11 Oxford Radcliffe http://www.controlledHospitals NHS trials.com/ISRCTN55089523 Trust (UK) Miscellaneous observational studies Type II Supracondylar Fractures in Children Prospective study NCT00207870 100 Child Oct-06 Jul-11 Type II Supracondylar Fractures Rec Interventions Conditions Recruit n Device: NovaLign Intramedullary Fixation System Fracture Rec 20 Children's Healthcare of Atlanta http://ClinicalTrials.gov/show/NCT00207870 A7B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Device NovaLign Intramedullary Fixation System (IFS) for the Treatment of Humeral Fractures Phase IV: Single group assignment, safety/efficacy study NCT00969839 135 Age Start (Grp) Date End Sponsors Date Adt Sep-09 Mar-11 NovaLign Sen Orthopaedics, Inc URL http://ClinicalTrials.gov/show/NCT00969839 Drugs including biologics A Dosing and Efficacy Study of Drug: sufentanil Intra-nasal Sufentanil for Moderate to Severe Pain Single group assignment, safety/efficacy study NCT01012999 Procedure Study Comparing Surgical Treatment Versus Non-surgical Treatment of Ulnar Fractures RCT NCT01123447 Pain; Opiate; upper or lower extremity fracture Term Procedure: Open Fracture; Trauma; Rec reduction and Ulna Fracture; internal fixation; Orthopedic; Surgery Procedure: Closed reduction and shortarm cast Forearm Shaft Fractures: Plating Procedure: Fractures of Radius Rec of Radius and Ulna Versus Plating intramedullary nailing and Ulna of Radius and Nailing of Ulna and plating; RCT, efficacy study Procedure: plating NCT01484366 A Trial of Plate Fixation Versus Procedure: Tension Displaced Olecranon Rec Tension Band Wire for Olecranon Band Wiring; Fractures Fractures Procedure: Plate RCT, efficacy study fixation NCT01391936 A Trial of Plate Fixation Versus Procedure: Tension Displaced Olecranon Rec Tension Band Wire for Olecranon Band Wiring; Fractures Fractures Procedure: Plate RCT, efficacy study fixation NCT01391936 Conservative versus surgical Bridging plate Humeral shaft Active interventions for treatment of the osteosynthesis; fracture humeral shaft fractures in adults Functional brace RCT ISRCTN24835397 Operative and Nonoperative Procedure: Open Humeral Mid-shaft Active, Treatment of Humeral Shaft reduction and Fractures NR Fractures internal fixation Phase III: RCT, safety/efficacy (ORIF); Other: Nonstudy surgical NCT00878319 16 Adt Nov-09 Mar-11 University of Sen Utah http://ClinicalTrials.gov/show/NCT01012999 100 Adt May-10 Dec-15 University of Sen Calgary (UK) http://ClinicalTrials.gov/show/NCT01123447 90 Adt Sep-10 Sep-13 Florida Sen Orthopaedic Institute http://ClinicalTrials.gov/show/NCT01484366 70 Child Sep-10 Sep-13 Royal Infirmary Adt of Edinburgh Sen http://ClinicalTrials.gov/show/NCT01391936 70 Child Sep-10 Sep-13 Royal Infirmary Adt of Edinburgh Sen http://ClinicalTrials.gov/show/NCT01391936 126 Adt Sen 180 Adt Aug-09 May-12 McGill University http://ClinicalTrials.gov/show/NCT00878319 Sen Health Center; Canadian Orthopaedic Trauma Society 136 Jul-10 Dec-12 Federal http://www.controlledUniversity of Sao trials.com/ISRCTN24835397 Paulo (Brazil) Effect of Osteosynthesis, Primary Procedure: NonProximal Humeral Rec 162 Adt Apr-09 Mar-12 Herlev Hospital Hemi-arthroplasty, and Nonsurgical Fractures Sen (Denmark) surgical Management for Fractures management; of the Proximal Humerus Procedure: Phase III: RCT Osteosynthesis; NCT00835562 Procedure: Hemiarthroplasty Open reduction and internal Open reduction + Comminuted, Comp 560 Sen Sep-08 Feb-12 German fixation versus closed reduction internal fixation; intraarticular distal Research and casting for highly comminuted, closed reduction + radial fractures Council intraarticular fractures of the distal casting (Germany) radius RCT ISRCTN76120052 Fluid Lavage of Open Wounds Saline solution Open fractures, Comp 2280 Adt Jun-09 Jan-12 McMaster (FLOW) gravity pressure (1 - upper or lower Sen University RCT 2 psi); Saline solution extremity (Canada) ISRCTN33993149 low pressure (5 - 10 psi); Saline solution high pressure (>20 psi); Castile soap solution (80 ml per 3 litres saline) gravity pressure (1 - 2 psi); Castile soap solution low pressure (5 - 10 psi); Castile soap solution high pressure (>20 psi) Clinical study of the volar locking Radial volar locking Distal radius fracture Comp 122 Child Feb-08 Aug-10 Nottingham plate for distal radial fractures plate; Conventional Adt University RCT method involving Sen Hospitals NHS ISRCTN27396017 percutaneous wires Trust (UK) +/- external fixator Management of Bone Defects Procedure: HMRS Tumor; Fracture; Rec 50 Child Dec-08 Jan-10 Medical Around the Elbow Cancer Adt University of Retrospective, cohort study Sen Vienna NCT00873145 137 http://ClinicalTrials.gov/show/NCT00835562 http://www.controlledtrials.com/ISRCTN76120052 http://www.controlledtrials.com/ISRCTN33993149 http://www.controlledtrials.com/ISRCTN27396017 http://ClinicalTrials.gov/show/NCT00873145 Other A Trial of Non-operative Versus Operative Management of Olecranon Fractures in the Elderly RCT, efficacy study NCT01397643 Reducing Range of Motion Deficits Post Radial Fracture RCT NCT01262807 Operative Versus Non Operative Treatment of Proximal Humerus (Shoulder Joint) Fractures Phase I: RCT, bio-equivalence study NCT00818987 Other: Nonoperative; Other: Operative Displaced Olecranon Fractures in Elderly Patients Rec 70 Sen Oct-10 Oct-13 Royal Infirmary of Edinburgh Other: Exercises Radius Fractures Rec 70 Other: Open reduction internal fixation; reduction and immobilization 3 and 4 Part Proximal Humerus Fractures Rec 120 Adt Dec-10 Dec-12 University of http://ClinicalTrials.gov/show/NCT01262807 Sen Manitoba; Pan Am Minor Injury Clinic Sen Nov-10 Oct-11 University of http://ClinicalTrials.gov/show/NCT00818987 British Columbia Miscellaneous observational studies A Clinical Investigation of the Discovery™ Elbow System Prospective, cohort study NCT00698867 Comparison of Two Radial Head Implants Retrospective, cohort study NCT01269840 Operative Versus Nonoperative Treatment of Humeral Shaft Fractures: A Prospective Cohort Comparison Study Prospective, cohort study NCT01363518 http://ClinicalTrials.gov/show/NCT01397643 Osteoarthritis; Invite Rheumatoid Arthritis; Avascular Necrosis; Humeral Fractures Radial Head Rec Fractures 120 Adt Jun-02 Jun-15 Biomet Sen Orthopedics, LLC 50 Closed Fracture of Shaft of Humerus 128 Adt Mar-10 Jul-11 Northwestern http://ClinicalTrials.gov/show/NCT01269840 Sen University; Rush University; North Shore University Hospital Adt May-10 May-11 St. Louis http://ClinicalTrials.gov/show/NCT01363518 University Invite 138 http://ClinicalTrials.gov/show/NCT00698867 A7C: OTHER Title Phases: trial design (control) CT ID Behavioural Eccentric Training With or Without Elbow Brace for Epicondylitis Phase III: RCT, efficacy study NCT01273688 Device Discovery Elbow Long-Term Survivorship Prospective, cohort study NCT01308463 Safety and Effectiveness Study of Ascension's PyroCarbon Radial Head Compared to Ascension's Metal Radial Head RCT, safety/efficacy study NCT00825409 Discovery Elbow Multi-Center Prospective Study Single group assignment NCT00515515 VIBration Training in EpicondylitiS Phase III: RCT, efficacy study NCT01269879 ExploR® Modular Radial Head Data Collection Prospective study NCT00533234 Interventions Conditions Behavioral: Eccentric Epicondylitis; training (Flex-Bar); Tendinopathy; Pain Device: EpiHit elbow brace Recruit n Not yet Rec 90 Age Start (Grp) Date End Sponsors Date Adt Feb-11 Nov-11 Hannover Sen Medical School URL http://ClinicalTrials.gov/show/NCT01273688 Device: Discovery elbow minimally constrained Elbow Pain Rec 120 Child Jan-10 Dec-20 Biomet, Inc. Adt Sen Device: Carbon Modular Radial Head; Device: Metal Radial Head Degenerative Arthritis; PostTraumatic Arthritis; Rheumatoid Arthritis Rec 203 Adt Jan-09 Jan-12 Ascension http://ClinicalTrials.gov/show/NCT00825409 Sen Orthopedics, Inc. Device: Discovery Elbow replacement Total Elbow Arthroplasty Wdrwn 40 Adt May-07 Dec-11 Vanderbilt Sen University; Biomet, Inc. http://ClinicalTrials.gov/show/NCT00515515 Not yet Rec 70 Adt http://ClinicalTrials.gov/show/NCT01269879 Term 50 Device: Flexi-Bar Epicondylitis; Pain; vibration device only; Tendinopathy Device: Flexi-Bar + XCO-Trainer Device: ExploR® Degenerative Modular Radial Head Conditions of the Radial Head/Neck; Post-traumatic Conditions of the Radial Head/Neck 139 Jan-11 Sep-11 Hannover Medical School Child Dec-09 Jun-10 Biomet Adt Orthopedics, Sen LLC http://ClinicalTrials.gov/show/NCT01308463 http://ClinicalTrials.gov/show/NCT00533234 Drugs including biologics The effect of dexmedetomidine in addition to local anaesthetic on the block of nerves in the arm RCT ISRCTN67622282 Levobupivacaine + Forearm and hand dexmedetomidine + surgery patients isotonic sodium chloride; Levobupivacaine + isotonic sodium chloride Drug: Xylocaine Forearm and Arm Surgery Comparison Between Two Different Volumes of Anesthesia Drug in Forearm Surgery Phase III: RCT, efficacy study NCT01216488 TENDOSHOCK-2010 Combination Drug: Polidocanol; Tendinopathy; Therapy for Athletic Device: Focused Epicondylitis; Tendinopathies extracorporeal shock Achilles, Patella, Phase II: Single group wave therapy; Drug: Elbow assignment, safety/efficacy Topical NO; study Behavioral: Painful NCT01185951 eccentric training in Achilles tendinopathy; Behavioral: Painful eccentric training for patella tendinopathy on 25° decline board; Behavioral: Painful eccentric training for elbow tendinopathy using Thera-Band Flex-Bar ED95 bupivacaine and Bupivacaine for Routine hand, supraclavicular block supraclavicular forearm or upper Single group assignment, brachial plexus block limb surgery safety/efficacy study ISRCTN63230740 Botulinum Toxin as a Novel Drug: Botulinum Post Traumatic Treatment for Prevention of Post- Toxin Type A; Drug: Stiffness Traumatic Elbow Stiffness Saline RCT, safety/efficacy study NCT01129583 Comp 64 Adt Nov-11 Feb-12 Cumhuriyet Sen University (Turkey) http://www.controlledtrials.com/ISRCTN67622282 Comp 72 Adt Jan-10 Jun-11 University Sen Hospital, Brest http://ClinicalTrials.gov/show/NCT01216488 Active, NR 114 Adt Jan-07 Dec-10 Hannover Sen Medical School http://ClinicalTrials.gov/show/NCT01185951 Comp 40 Adt Oct-09 Oct-10 University of Sen Leeds (UK) http://www.controlledtrials.com/ISRCTN63230740 Comp 18 Adt Nov-03 May-10 Columbia Sen University; Allergan http://ClinicalTrials.gov/show/NCT01129583 140 Ultrasound-guided Axillary Plexus Block - Dose Reduction of Prilocaine Phase IV: Non-randomized, parallel assignment, safety/efficacy study NCT01309360 Procedure Human Upper Extremity Allotransplantation Phase II: Single group assignment, safety/efficacy study NCT01459107 Preservation of Joint Function Using Postoperative Continuous Passive Motion (CPM) A Pilot Study Phase III: RCT, efficacy study NCT01420887 Uncemented Total Elbow Arthroplasty Data Collection Prospective study NCT00974298 Early Discharge in Patients Undergoing Elbow Arthroscopy RCT NCT01151241 Prevention of Phantom Limb and Stump Pain Using Ambulatory Continuous Peripheral Nerve Blocks Phase IV: RCT, safety/efficacy study NCT00771862 Drug: midazolam; Drug: prilocaine 1%; Drug: prilocaine 1%; Drug: prilocaine 1% Other Surgical Comp Procedures; elective surgery on the distal forearm or the hand incl. for carpal tunnel sydrome Procedure: Amputation, Deceased donor Traumatic; Wounds hand transplantation; and Injuries; Hand Drug: Bone marrow Injuries cell-based therapy & single-drug immunosuppression. Procedure: Elbow Injury Continuous Passive Motion; Procedure: Physical Therapy Procedure: Total elbow replacement arthroplasty Total Elbow Arthroplasty 120 Adt Sep-09 Apr-10 Helios Research http://ClinicalTrials.gov/show/NCT01309360 Sen Center Rec 30 Adt Sen Not yet Rec 50 Child Aug-11 Jul-14 Mayo Clinic Adt Sen http://ClinicalTrials.gov/show/NCT01420887 Rec 100 Adt Mar-09 Mar-14 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00974298 40 Adt 18 Adt Oct-08 Dec-12 University of http://ClinicalTrials.gov/show/NCT00771862 Sen California, San Diego; National Institute of General Medical Sciences (NIGMS) Procedure: Elbow Elbow Arthroscopy Rec arthroscopy with Surgery infraclavicular nerve block and continuous local anesthetic infusion to day 3 post op.; Other: Early Discharge; Other: Normal Discharge Procedure: Amputation; Active, perineural ropivicaine Phantom Limb Pain; NR Stump Pain 141 Jul-11 Jun-21 Johns Hopkins University http://ClinicalTrials.gov/show/NCT01459107 Jul-10 Apr-13 University Health http://ClinicalTrials.gov/show/NCT01151241 Network, Toronto Ambulatory Continuous Peripheral Procedure: Nerve Blocks for Treatment of perineural Post-Amputation Phantom Limb ropivacaine and Stump Pain RCT, efficacy study NCT00667264 Amputation; Phantom Limb; Stump Pain Comp 7 Evaluation the Operative Procedure: tear of Procedure Among Patients That the distal tendon in Suffer From Tear of the Distal the biceps muscle Tendon of the Biceps Retrospective, case-crossover study NCT01343875 Prospective Biceps Study Procedure: Distal Prospective, cohort study Biceps Re-Insertion NCT01317719 Surgery Perineural Catheter Insertion Procedure: Sciatic Distance for Continuous Peripheral catheter left 0-1cm Nerve Blocks past needle tip vs. 5Phase IV: RCT, safety/efficacy 6cm past needle tip study NCT00997867 Elaboration of a Pre-surgery Procedure: fMRI; Mapping Protocol of Primary Motor Procedure: mTMS Cortex, Prior to an Implementation of a Stimulation of Primary Motor Cortex for Patients With Deafferentiation of Brachial Plexus Pain Non-randomized, parallel assignment NCT01104506 Trial Comparing Single Versus Procedure: Distal Double Incision to Repair Distal bicep tendon Bicep Tendon Ruptures reconstruction RCT NCT01322828 Biceps Tendon Rupture Not yet N/K Rec Adt Oct-08 Dec-11 University of http://ClinicalTrials.gov/show/NCT00667264 Sen California, San Diego; Summit Medical; National Institute of General Medical Sciences (NIGMS) Adt N/K Dec-11 Hadassah http://ClinicalTrials.gov/show/NCT01343875 Medical Organization Jan-11 West Penn http://ClinicalTrials.gov/show/NCT01317719 Allegheny Health System Adt Nov-09 Oct-10 University of http://ClinicalTrials.gov/show/NCT00997867 Sen California, San Diego Biceps Tendon Rupture Invite N/K Lower Extremity Surgery; Upper Extremity Surgery; Post-operative Pain Comp 350 Painful Avulsion of Brachial Plexus Term 13 Adt Apr-10 Sep-10 Nantes Sen University Hospital Distal Bicep Tendon Rupture Comp 92 Adt Mar-04 Jan-10 Hand and Upper http://ClinicalTrials.gov/show/NCT01322828 Sen Limb Clinic, Canada 142 Adt Sen N/K http://ClinicalTrials.gov/show/NCT01104506 Optimization of Catheter Insertion Site for Continuous Peripheral Nerve Blocks Phase IV: RCT, safety/efficacy study NCT00876746 Procedure: Supraclavicular vs. Infraclavicular ropivicaine infusion Other Interface Kinematics of Other: Socket Transhumeral Prosthetic Sockets Using XROMM Prospective, case-crossover study NCT01546675 Upper-extremity Surgery; Postoperative Pain Traumatic Amputation of Arm Comp 60 Adt Dec-08 Jan-10 University of Sen California, San Diego http://ClinicalTrials.gov/show/NCT00876746 Rec 2 Adt Jan-12 Mar-13 Providence VA http://ClinicalTrials.gov/show/NCT01546675 Sen Medical Center; Department of Veterans Affairs Recruit n Age Start (Grp) Date 79 Child Jan-09 May-10 Orthopedic http://ClinicalTrials.gov/show/NCT01133938 Hospital Vienna Speising A8. HIP A8A: PAEDIATRICS Title Interventions Phases: trial design (control) CT ID Miscellaneous observational studies Predictive Factors for the Development of Osteonecrosis After the Treatment of the Developmental Dislocated Hip Retrospective, cohort study NCT01133938 Conditions Predictors of Comp Osteonecrosis of the Femoral Head After Treatment of the Dislocated Hip 143 End Sponsors Date URL A8B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Behavioural Enhanced Rehabilitation for Elderly People With a Hip Fracture and Depression Phase II: RCT, efficacy study NCT00951691 Efficacy of a Post-Rehabilitation Exercise Intervention RCT NCT00592813 Interventions Conditions Recruit n Behavioral: Enhanced acute medical rehabilitation; Behavioral: Treatment as usual Behavioral: Enhanced Strong for Life; Behavioral: cardiovascular nutrition education Hip Fracture; Depression Rec 40 Adt Aug-09 Dec-12 National Institute http://ClinicalTrials.gov/show/NCT00951691 Sen of Mental Health (NIMH) Hip Fracture; Disability Rec 230 Invite 30 Adt Apr-08 Jul-12 Boston http://ClinicalTrials.gov/show/NCT00592813 Sen University; National Institute of Nursing Research; Spaulding Rehabilitation Hospital Child Nov-10 May-12 Meir Medical http://ClinicalTrials.gov/show/NCT01234844 Adt Center Sen The Relationship Between Pet Behavioral: care of Therapy and “Well-being” in guinea pigs; Geriatric Rehabilitation In-patients" Behavioral: guinea Single group assignment pigs NCT01234844 Cerebrovascular Accident; Hip Fracture Device AMIStem Primary Hip System Device: AMIStem Hip Osteoarthritis; Prospective Post-marketing Multi- System Arthritis; Avascular centre Surveillance Study Necrosis; Fracture of Single group assignment, the Femoral Neck or safety/efficacy study Head; Congenital NCT01107340 Hip Dysplasia Rec Age Start (Grp) Date End Sponsors Date URL 500 Child Feb-10 Feb-24 Medacta http://ClinicalTrials.gov/show/NCT01107340 Adt International SA Sen 144 A Multi-centre Study to Assess the Device: DePuy ASR Long-term Performance of the Hip System DePuy ASR™ System in Primary Hip Resurfacing Surgery Phase IV: Single group assignment, safety/efficacy study NCT00208377 Rheumatoid Arthritis; Term Osteoarthritis; Posttraumatic Arthritis; Collagen Disorders; Avascular Necrosis; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis. Post-Market Study of the Modular Device: Modular Asceptic Loosening; Rec Revision Hip System Revision Hip System Osteolysis; Prospective, cohort study Traumatic Fracture; NCT01464645 Failed Total Hip Implant Using Alternative Implants for the Device: Open Femoral Neck Rec Surgical Treatment of Hip reduction internal Fractures Fractures (The FAITH Study) fixation (ORIF) with Phase III: RCT, efficacy study single sliding hip NCT00761813 screw; Device: ORIF with multiple cancellous screws Post-Operative Delirium in Elderly Surgical Patients RCT, efficacy study NCT00590707 Device: Maintenance Hip Fractures; of level of awareness Delirium by use of a BIS monitor & the OASS; Device: Maintenance of level of awareness by use of a BIS monitor and the OASS. Rec 228 Adt Jul-03 Jul-20 DePuy International http://ClinicalTrials.gov/show/NCT00208377 200 Adt Jan-12 Dec-17 Encore Medical, http://ClinicalTrials.gov/show/NCT01464645 Sen L.P.; DJO Incorporated 1500 Adt Mar-09 Mar-16 National Institute http://ClinicalTrials.gov/show/NCT00761813 Sen of Arthritis and Musculoskeletal and Skin Diseases; Canadian Institutes of Health Research; Stichting Nuts Ohra (SNO); Physicians Services Incorporated (PSI) Foundation 210 Adt Jan-05 Dec-15 Johns Hopkins http://ClinicalTrials.gov/show/NCT00590707 Sen University; National Institutes of Health 145 Proximal Femoral Nail Antirotation (PFNA) Versus PFNA Augmentation Phase IV: RCT, efficacy study NCT01473082 Proximal Femur Locking Compression Plates Versus Trochanteric Nails Phase IV: Non-randomized, parallel assignment NCT01128868 Treatment of Intertrochanteric Fracture With New Type of Intramedullary Nail Phase IV: RCT, safety/efficacy study NCT01437176 Treatment of Acetabular Posterior Wall Fracture With Anatomical Locking Plate Phase IV: RCT, safety/efficacy study NCT01437150 Cemented vs Non-cemented Semiendoprosthesis in the Treatment of Proximal Femoral Fractures RCT, safety/efficacy study NCT00859378 Device: PFNA Augmentation (Synthes); Device: PFNA (Synthes) Hip Fractures; Closed Fracture of Hip Rec 144 Sen Feb-12 Dec-15 AO Clinical http://ClinicalTrials.gov/show/NCT01473082 Investigation and Documentation Reverse Oblique Intertrochanteric Fractures; Reverse Oblique Subtrochanteric Fractures Device: new type of Intertrochanteric intramedullary nail; Fracture Device: The intramedullary nail of PFNA Rec 112 Adt May-11 Sep-13 AO Clinical http://ClinicalTrials.gov/show/NCT01128868 Sen Investigation and Documentation Rec 36 Adt Sep-11 Aug-13 Peifu Tang Sen http://ClinicalTrials.gov/show/NCT01437176 Device: Anatomical Fracture of locking plate; Acetabulum Procedure: The Reconstructive Plate Rec 36 Adt Aug-11 Jul-13 Peifu Tang Sen http://ClinicalTrials.gov/show/NCT01437150 Device: Cemented Hip Fracture; semiendoprosthesis; Proximal Femoral Device: nonFracture cemented Rec 400 Child Oct-08 Dec-12 Kuopio http://ClinicalTrials.gov/show/NCT00859378 Adt University Sen Hospital; The Finnish Foundation of Orthopedics and Traumatology 200 Adt Feb-07 Dec-12 McGill University http://ClinicalTrials.gov/show/NCT00597779 Sen Health Center; Orthopaedic Trauma Association 40 Adt May-07 Dec-12 Chinese http://ClinicalTrials.gov/show/NCT01293721 Sen University of Hong Kong Fonly Randomized Comparison of 2 Fixation Techniques for Unstable Intertrochanteric Hip Fractures Phase III: RCT, efficacy study NCT00597779 Study of Low-Magnitude, HighFrequency Vibration Treatment on Osteoporotic Hip Fracture Healing Phase II/III: RCT, safety/efficacy study NCT01293721 Device: Dynamic Hip Hip Fractures Screw (DHS); Trochanteric Fixation Nail (TFN) Device: Proximal femur locking plate; Device: Intertrochanteric nail Device: Lowmagnitude high frequency vibration treatment Hip Fracture Active, NR Rec 146 InterTAN IM Nail Versus Sliding Hip Screw in Geriatric Fractures RCT NCT00664950 Device: sliding hip screw; Device: IntertAn IM nail Hip Fractures Comparing Weight Bearing After Intramedullary Fixation Devices for the Proximal Femur Fracture Phase IV: RCT, efficacy study NCT01509859 Device: PFNA proximal femur nail device (Synthes); Device: INTERTAN proximal femur nail device (Smith&Nephew) Hip Protector for Prevention of Hip Fracture Phase III: RCT, safety/efficacy study NCT01017341 Neck of femur Optimisation Therapy-Targeted Stroke volume RCT ISRCTN88284896 Comparison of Gamma Nail Versus Dynamic Hip Screw for the Treatment of Unstable Intertrochanteric Fractures RCT, efficacy study NCT01173744 Role of Vacuum Assisted Closure (VAC) Device in Postoperative Management of Pelvic and Acetabular Fractures RCT, efficacy study NCT00635479 Device: PSU hip protector Closed Comminuted Rec 100 Oblique Intertrochanteric Fracture of Neck of Right Femur; Closed Comminuted Oblique Intertrochanteric Fracture of Neck of Left Femur Hip Fracture Not yet 200 Rec LiDCO machine Device: Gamma-3 Nail; Device: DHS Surgical repair of fracture to neck of femur under spinal anaesthesia Intertrochanteric Femoral Fractures Device: Wound Vac; Pelvic Bone Other: Gauze Fractures; dressing Acetabular Fracture; Hip Fractures Rec 240 Active 130 Rec 60 Rec 200 147 Adt Nov-07 Nov-12 Lawson Health Sen Research Institute; Orthopaedic Research Foundation Adt Dec-11 Sep-12 Rabin Medical Sen Center http://ClinicalTrials.gov/show/NCT00664950 Adt Jun-10 Sep-12 Prince of Sen Songkla University http://ClinicalTrials.gov/show/NCT01017341 http://ClinicalTrials.gov/show/NCT01509859 Adt Jan-09 Aug-12 Nottingham http://www.controlledSen University trials.com/ISRCTN88284896 Hospitals NHS Trust (UK) Adt Jul-10 Jul-12 Wolfson Medical http://ClinicalTrials.gov/show/NCT01173744 Sen Center Adt Mar-08 Jun-12 University of http://ClinicalTrials.gov/show/NCT00635479 Sen MissouriColumbia; University of California, Davis; University of Alabama at Birmingham; Medical College of Wisconsin Treatment of Unstable Trochanteric Fractures With the Proximal Femoral Nail Antirotation (PFNA)-Asia Prospective, case-only study NCT00873548 Comparison Study of 3-4-screwsinternal Fixation With Multi-screwsystem Targon FN for Femoral Neck Fracture Phase IV: RCT, efficacy study NCT00829725 Intracapsular Femoral Neck Fractures Fixation With a Dynamic Locking Plate and Screw System, Targon FN Single group assignment, safety/efficacy study NCT00830687 Comparison Between Gamma 3 Nail and ACE Trochanteric Nail Single group assignment, efficacy study NCT00367406 Comparison of the Results of Treatment by Gamma Nail Versus Dynamic Hip Screw for Unstable Intertrochanteric Hip Fractures RCT NCT01238068 Influence of Bone Strength Measured by DensiProbe on Bone Related Fixation Failure Single group assignment NCT00822159 Device: PFNA-Asia Trochanteric Fractures Active, NR 298 Adt Nov-07 Mar-12 AO Clinical http://ClinicalTrials.gov/show/NCT00873548 Sen Investigation and Documentation; Synthes Inc. Device: screwsFemoral Neck internal fixation; Fractures Device: TARGON FN Rec 300 Adt Jan-09 Jan-12 Sheba Medical Sen Center http://ClinicalTrials.gov/show/NCT00829725 Device: TARGON FN Femoral Neck Fractures Rec 100 Adt Jan-09 Jan-12 Sheba Medical Sen Center http://ClinicalTrials.gov/show/NCT00830687 Device: Gamma 3 nail versus ACE trochanteric nail Rec 100 Adt Nov-06 Dec-11 University http://ClinicalTrials.gov/show/NCT00367406 Sen Hospital, Ghent Device: gamma nail Intertrochanteric stryker Fractures of the Hip Not yet Rec 60 Adt Nov-10 Nov-11 Tel-Aviv Sen Sourasky Medical Center Device: DensiProbe Femoral Fractures; Hip Hip Fractures; Osteoporosis; Bone Density Term 198 Adt Nov-08 Sep-11 AO Clinical http://ClinicalTrials.gov/show/NCT00822159 Sen Investigation and Documentation Pertrochanteric and Subtrochanteric Femur Fractures 148 http://ClinicalTrials.gov/show/NCT01238068 A Single Centre Study to Assess Device: DePuy the Long-term Performance of the ASR™ Hip System DePuy ASR™ System in Primary Hip Resurfacing Surgery Phase IV: Single group assignment, safety/efficacy study NCT00872794 Evaluation of the Proximal Femoral Device: Proximal Nail Antirotation With Cement Femoral Nail Augmentation in Osteoporotic Antirotation(PFNA) Femoral Neck Fractures with cement Phase I/II: Single group augmentation assignment NCT01235169 Comparison of Treatment Device: 2 Versus 4 Outcomes in Hip Fractures Hole DHS Surgically Fixed With Either a Two or Four Hole Device. Phase IV: RCT, safety/efficacy study NCT00323232 Retrospective Study of the Device: Encore Linear™ Hip Linear™ Hip System Phase IV: Retrospective, cohort study NCT00764959 Proximal Femoral Nail Antirotation™ (PFNA) Versus Gamma Nail 3™ (Gamma3) for Intramedullary Nailing of Unstable Trochanteric Fractures Phase IV: RCT, efficacy study NCT00736684 Device: Proximal Femoral Nail Antirotation™ (PFNA); Device: Gamma Nail 3™ (Gamma3) Adt Nov-03 Sep-11 DePuy International http://ClinicalTrials.gov/show/NCT00872794 Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT01235169 Rheumatoid Arthritis; Term Osteoarthritis; Posttraumatic Arthritis; Collagen Disorders; Avascular Necrosis; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis. Proximal Femur Not yet Fracture Rec 50 Hip Fracture Comp 400 Adt Dec-10 Apr-11 University of http://ClinicalTrials.gov/show/NCT00323232 Sen British Columbia Osteoarthritis; Term Rheumatoid Arthritis; Femoral Fracture; Correction of a Functional Deformity; Avascular Necrosis Unstable Comp Trochanteric Fractures 200 Adt Oct-07 Feb-11 Encore Medical, http://ClinicalTrials.gov/show/NCT00764959 Sen L.P. 440 Adt Nov-07 Sep-10 AO Clinical http://ClinicalTrials.gov/show/NCT00736684 Sen Investigation and Documentation; Synthes Inc. Adt Sen 149 Clinical Evaluation on HA Coated Dynamic Hip Screws for Trochanteric Femoral Fractures RCT, safety/efficacy study NCT00756431 Device: Hip Fracture Osteoarthritis reduction Screw without HA Coating (Hiploc); Device: Hip Fracture reduction Screw with HA Coating (Hiploc) Fixation using Alternative Implants Sliding hip screws; Femoral neck for the Treatment of Hip fractures Cancellous screws fractures (FAITH): a multi-centre randomised trial comparing sliding hip screws and cancellous screws on revision surgery rates and quality of life in the treatment of femoral neck fractures RCT ISRCTN25524122 Dietary supplements Hip Fracture Surgery and Oral Dietary Supplement: Hip Fracture Nutritional Supplements Oral nutritional Phase III: RCT, safety/efficacy Supplement; Dietary study Supplement: Placebo NCT01505985 Hyperprotein Nutritional Dietary Supplement: Sarcopenia; Hip Intervention in Elderly Patients Ensure Plus Fracture With Hip Fracture and Sarcopenia Advance RCT, efficacy study NCT01404195 Nutritional Intervention for Geriatric Dietary Supplement: Hip Fractures Hip Fracture Patients Protein RCT, efficacy study supplementation NCT01088139 Nutritional Intervention in Hip Dietary Supplement: Hip Fracture; Fracture Patients Cubitan Malnutrition RCT, efficacy study NCT00523575 Wdrwn 0 Child Jan-04 Jun-10 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT00756431 Adt Hvidovre Sen University Hospital; Biomet U.K. Ltd. Comp 80 Adt Jun-08 Jan-10 McMaster Sen University (Canada) Rec 192 Sen Jan-12 Jul-14 Nestlé Nutrition http://ClinicalTrials.gov/show/NCT01505985 Corporate Rec 100 Adt Jan-12 Mar-13 Hospital San Sen Juan de Dios, Spain http://ClinicalTrials.gov/show/NCT01404195 Comp 126 Adt Nov-08 Apr-11 Kowloon Sen Hospital, Hong Kong http://ClinicalTrials.gov/show/NCT01088139 Comp 210 Adt Aug-07 Jun-10 Maastricht http://ClinicalTrials.gov/show/NCT00523575 Sen University Medical Center; ZonMw: The Netherlands Organisation for Health Research and Development 150 http://www.controlledtrials.com/ISRCTN25524122 Drugs including biologics Effect of Teriparatide on Hip Fracture Healing Phase III: RCT, efficacy study NCT01473589 Second Study of the Effect of Teriparatide on Hip Fracture Healing Phase III: RCT, efficacy study NCT01473602 A Study That Will Compare the Effect of Two Drugs on Patients With Low Bone Mass and a Recent Hip Fracture Phase IV: RCT, efficacy study NCT00887354 Statin in Hip Fracture Phase III: RCT, safety/efficacy study NCT01494090 Postoperative Blood Transfusion for Frail Elderly With Hip Fracture RCT, safety/efficacy study NCT01102010 Study To Assess Fracture Healing With Sclerostin Antibody Phase II: RCT, safety/efficacy study NCT01081678 Study of the Effect of Tranexamic Acid Administered to Patients With Hip Fractures. Can Blood Loss be Reduced? RCT, safety/efficacy study NCT01535781 Parathyroid hormone in the recovery from hip fractures: a pilot study RCT, pilot study ISRCTN03362357 Drug: Teriparatide; Drug: Placebo Femur Neck Fracture Rec 1220 Adt Feb-12 Oct-15 Eli Lilly and Sen Company http://ClinicalTrials.gov/show/NCT01473589 Drug: Teriparatide; Drug: Placebo Femur Neck Fracture Rec 1220 Adt Jan-12 Oct-15 Eli Lilly and Sen Company http://ClinicalTrials.gov/show/NCT01473602 Drug: Teriparatide; Drug: Risedronate; Drug: Placebo, weekly; Drug: Placebo, daily Osteoporosis Rec 242 http://ClinicalTrials.gov/show/NCT00887354 Drug: Rosuvastatin; Hip Fracture Drug: Placebo Rec Biological: Blood transfusion Rec 1222 Adt Aug-11 Mar-14 University http://ClinicalTrials.gov/show/NCT01494090 Sen Hospital, Brest; Ministry of Health, France 284 Adt Jan-10 Dec-13 University of http://ClinicalTrials.gov/show/NCT01102010 Sen Aarhus Hip Fracture Drug: Placebo; Drug: Fracture Healing; AMG 785 140 mg; Hip Drug: AMG785 70mg; Drug: AMG 785 210mg Drug: Tranexamic Hip Fracture; Acid; Drug: Placebo Anemia Tereparatide Hip fracture (Forsteo®) 20 µg/day injections; Standard care Adt Apr-09 Jul-14 Eli Lilly and Sen Company Rec 330 Adt Jun-10 Dec-13 Amgen Sen http://ClinicalTrials.gov/show/NCT01081678 Rec 120 Adt Sep-11 Sep-13 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01535781 Active 40 Adt Jan-11 May-13 North Bristol http://www.controlledSen NHS Trust (UK) trials.com/ISRCTN03362357 151 Preoperative Levosimendan and Heart Failure Phase IV: RCT, safety/efficacy study NCT01022983 Norspan Versus Oxycontin as Postoperative Painkiller to Proximal Extracapsular Fractures of the Femur Phase IV: RCT, efficacy study NCT00964808 Efficacy and Safety of Intravenous Iron Sucrose in Patients With Hip Fracture to Prevent Perioperative Anemia Phase IV: RCT, safety/efficacy study NCT01084122 Intravenous Acetaminophen as Adjuvant Therapy for Pain Control in Geriatric Hip Fracture Patients Phase III: RCT, efficacy study NCT01520298 Effectiveness of Two Types of Treatment in Restoring Muscle After Hip or Knee Surgery Phase II: RCT, efficacy study NCT00393848 Drug: Levosimendan; Heart Failure; Hip Drug: Placebo Fracture Rec 70 Drug: Buprenorphine; Drug: Oxycodone Pain, Postoperative Rec 50 Drug: Iron sucrose Hip Fracture; Not yet 360 Surgical Intervention Rec Drug: Essential amino acid supplement; Drug: Ketoconazole; Drug: Whey protein Intrathecal Morphine,Femoral Nerve Block,Periarticular Bupivacaine Infiltration for Pain After Intramedullary Hip Screw Phase IV: RCT, efficacy study NCT01219088 Hip Fracture Surgery in Elderly Patients Phase II: RCT, efficacy study NCT01199276 Drug: Placebo; Drug: Pain; Hip Fracture Acetaminophen IV Adt Apr-11 Feb-13 Sykehuset i http://ClinicalTrials.gov/show/NCT01022983 Sen Vestfold HF; Orion Corporation, Orion Pharma Adt Sep-09 Jan-13 Vejle Hospital; http://ClinicalTrials.gov/show/NCT00964808 Sen Norpharma A/S Adt May-10 Dec-12 Hospital Clinic of http://ClinicalTrials.gov/show/NCT01084122 Sen Barcelona Rec 46 Adt Dec-11 Dec-12 Lancaster http://ClinicalTrials.gov/show/NCT01520298 Sen General Hospital Hip Fracture; Osteoarthritis; Femur Head Necrosis Active, NR 120 Drug: Bupivacaine, morphine Femoral Neck Fractures Rec 80 Adt Oct-06 Oct-12 University of http://ClinicalTrials.gov/show/NCT00393848 Sen Arkansas; National Institute of Arthritis and Musculoskeletal and Skin Diseases Adt Sep-10 Sep-12 Mahidol http://ClinicalTrials.gov/show/NCT01219088 Sen University Drug: Xenon; Drug: Sevoflurane Delirium Rec 256 152 Sen Sep-10 Sep-12 Air Liquide http://ClinicalTrials.gov/show/NCT01199276 Santé International; i3 Innovus Hemostasis in Kocher-Langenbeck Biological: Vitagel Fracture Fixation; Approaches for Acetabular topical surgical Intra-Articular Surgery Using a Topical Surgical hemostat Fractures; Hemostat (Vitagel) Acetabulum Phase IV: RCT, efficacy study NCT01230931 Impact of Pre-surgical Nasal Drug: 3M Skin and Surgical Site Infection; displaced Bacterial Reduction on Nasal Antiseptic hip fractures; spinal Postoperative Surgical Site instability/fractures Infections Phase IV: Single group assignment NCT01148030 Single Dose of Dexamethasone in Drug: Fractured Neck of Femur Fractures Dexamethasone Femur Phase IV: RCT, efficacy study acetate; Drug: NCT01550146 Placebo TRAUMEEL for Pain After Fracture Drug: Traumeel S; Pain; Fracture of of Neck of Femur Drug: Placebo Neck of Femur Phase III: RCT, efficacy study remedy NCT00307905 A Non-inferiority Study Comparing Biological: Heparin Hip Fracture Surgery Two Heparin Sodium Preparations Sodium - Eurofarma; in Hip Fracture Surgery Biological: Heparin Phase III: RCT, safety/efficacy Sodium - APP study Pharmaceuticals NCT01352039 Ropivacaine Hypobaric Spinal Drug: 6 mg of Femoral Neck Anaesthesia in Traumatic Hip ropivacaine; Drug: 8 Fracture Surgery mg of ropivacaine; Phase IV: RCT, safety/efficacy Drug: 10 mg of study ropivacaine; Drug: 12 NCT01005550 mg of ropivacaine Comparing Different Routes and Drug: Phytonadione; Bleeding; Doses of Phytonadione (Vitamin K) Drug: Phytonadione Complications for Reversing Warfarin Treated Patients With Hip Fracture Before Surgery RCT, efficacy study NCT00905229 Rec 50 Rec 400 Child Jun-10 Jul-12 3M Adt Sen Rec 40 Wdrwn 224 Adt Adt Sen Oct-10 Jul-12 The University of http://ClinicalTrials.gov/show/NCT01230931 Texas Health Science Center, Houston http://ClinicalTrials.gov/show/NCT01148030 Jul-09 Jul-12 Cork University http://ClinicalTrials.gov/show/NCT01550146 Hospital; University of Bristol Adt Jan-11 Jun-12 Shaare Zedek http://ClinicalTrials.gov/show/NCT00307905 Sen Medical Center Not yet 544 Rec Adt Oct-11 Mar-12 Eurofarma Sen Laboratorios S.A. http://ClinicalTrials.gov/show/NCT01352039 Comp 64 Sen Apr-09 Mar-12 Hospices Civils de Lyon http://ClinicalTrials.gov/show/NCT01005550 Not yet Rec 60 Adt May-09 Mar-12 HaEmek Medical http://ClinicalTrials.gov/show/NCT00905229 Sen Center, Israel 153 Efficacy of Ferric Carboxymaltose With or Without Erythropoietin Versus Placebo in Reducing Redcell Transfusion Packs in Hip Fracture Perioperative Period Phase III: RCT, efficacy study NCT01154491 A Dose Finding Study for Pain Relief of a Broken Hip Phase IV: Non-randomized, single group assignement, safety/efficacy study NCT00926666 Postoperative Analgesia With Local Infiltration After Hip Fracture Of Intertrochanteric Type Phase IV: RCT, efficacy study NCT01119209 Femoral nerve blockade in hip fracture patients RCT ISRCTN46653818 Does Omeprazole Decrease Intestinal Calcium Absorption? Phase IV: Single group assignment NCT00582972 Drug: Ferric Hip Fractures carboxymaltose; Drug: Ferric carboxymaltose and Erythropoetin; Drug: Placebo Perioperative Analgesia by Femoral Perineural Catheter for Femoral Neck Fracture - Study KTcol Phase IV: RCT, efficacy study NCT01052974 Feasibility And Safety Study Of rhBMP-2/CPM For Hip Fractures Phase II: RCT, safety study NCT00384358 Drug: ropivacaine Rec 306 Adt Jun-10 Jun-11 Fundación http://ClinicalTrials.gov/show/NCT01154491 Sen Pública Andaluza para la gestión de la Investigación en Sevilla Adt Oct-09 Apr-11 NHS Greater Sen Glasgow and Clyde; Chief Scientist Office of the Scottish Government Child Feb-08 Jan-11 Odense Adt University Sen Hospital Drug: Levobupivacaine Femoral Neck Fractures Not yet Rec 48 Drug: Ropivacaine; Drug: Saline Hip Fracture of Intertrochanteric Type Comp 74 Femoral nerve blockade; Regular use of opioids Hip fracture Comp 250 Sen Mar-09 Dec-10 Umeå University http://www.controlled(Sweden) trials.com/ISRCTN46653818 Drug: Omeprazole Osteoporosis; Comp Achlorhydria; GERD; Hip Fracture 21 Child Jan-08 Dec-10 University of Adt Wisconsin, Sen Madison Femoral Neck Fracture Drug: rhBMP-2/CPM; Fractures Drug: rhBMP-2/CPM; Other: surgical intervention alone Rec 60 Comp 108 154 http://ClinicalTrials.gov/show/NCT00926666 http://ClinicalTrials.gov/show/NCT01119209 http://ClinicalTrials.gov/show/NCT00582972 Fonly Adt Mar-09 Sep-10 University http://ClinicalTrials.gov/show/NCT01052974 Sen Hospital, Angers Adt Dec-06 Jun-10 Wyeth is now a Sen wholly owned subsidiary of Pfizer http://ClinicalTrials.gov/show/NCT00384358 Prevention of Venous Drug: YM150 Thromboembolism in Subjects Undergoing Hip Fracture Surgery or Surgery in the Lower Extremities Phase III: Non-randomized, single group assignement, safety/efficacy study NCT00937911 Comparison of the post-operative Fascia iliaca pain relief provided by the compartment block 1 administration of either a femoral mg/kg OR 1.5 mg/kg nerve block or fascia iliaca levobupivacaine; compartment block at one of two Femoral nerve block different doses in patients 1 mg/kg OR 1.5 undergoing surgery for hip fracture mg/kg RCT levobupivacaine ISRCTN51569968 Study of DU-176b, Prevention of Drug: DU-176b Venous Thromboembolism in (edoxaban); Drug: Patients After Hip Fracture Surgery Enoxaparin sodium Phase III: RCT, safety/efficacy 20mg study NCT01181141 Evaluation of AVE5026 as Drug: Semuloparin Compared to Placebo for the sodium (AVE5026); Extended Prophylaxis of Venous Drug: Placebo Thromboembolism in Patients Having Undergone Hip Fracture Surgery Phase III: RCT, efficacy study NCT00709904 Procedure Intramedullary Nail Versus Sliding Hip Screw Inter-Trochanteric Evaluation RCT NCT01380444 A Comparison of Two Pain Control Techniques on Deliruim in Hip Fracture Patients RCT, efficacy study NCT01547468 Procedure: Gamma3 Intramedullary Nails (Stryker); Procedure: Sliding Hip Screws Venous Thromboembolism Comp 101 Adt Jun-09 Apr-10 Astellas Pharma http://ClinicalTrials.gov/show/NCT00937911 Sen Inc Fractured neck of femur Term 120 Adt Aug-09 Feb-10 Belfast Health http://www.controlledSen and Social Care trials.com/ISRCTN51569968 Trust (UK) Venous Thromboembolism Comp 92 Adt Oct-08 Feb-10 Daiichi Sankyo http://ClinicalTrials.gov/show/NCT01181141 Sen Inc.; Daiichi Sankyo, Tokyo, LTD. Venous Thromboembolism Comp 469 Adt Jun-08 Jan-10 Sanofi-Aventis Sen Rec 736 Rec 270 Adt Dec-11 Dec-15 Stryker Trauma http://ClinicalTrials.gov/show/NCT01380444 Sen GmbH; Stryker Osteosynthesis; Global Research Solutions Adt Mar-12 Mar-15 Leslie Thomas; http://ClinicalTrials.gov/show/NCT01547468 Sen American Society of Anesthesiologist s Femoral Neck Fractures; Intertrochanteric Fracture Procedure: Femoral Hip Fracture Nerve Catheterization; Procedure: Intravenous Opioids 155 http://ClinicalTrials.gov/show/NCT00709904 Eva-Hip, Evaluation of Rehabilitation After Hip-fracture Phase I/II: RCT NCT01379456 Procedure: physiotherapy Hip Fracture Rec 100 Rec 108 Rec 200 Hip Fracture; Aged Active, NR 400 Left Ventricular Dysfunction; Femoral Fracture Not yet 200 Rec On the Impact of Bleeding on Two Procedure: MISS; Surgical Treatment Strategies Osteosynthesis of Procedure: PHS Trochanteric Fractures Phase IV: RCT NCT01427036 Improving Pain and Function in Hip Procedure: Femoral Pain; Hip Fractures Fracture Nerve Block Phase III: RCT, efficacy study NCT00749489 A New Clinical Pathway for Procedure: geriatric Patients With Fractured Neck of work-up; Procedure: Femur Orthopedic Phase II: RCT, safety/efficacy study NCT00667914 Optimization Study of Cardiac Risk Procedure: Colloids, Patients With Hip Fracture dobutamin, RCT, efficacy study levosimendan NCT01219712 Prospective Trial on Trochanteric Femur Fractures Treated With or Without a Trochanter Support Plate RCT, efficacy study NCT00626470 Procedure: Addition Femoral Fractures of TSP to DHS Rec 100 156 Sen Feb-11 Dec-14 Norwegian http://ClinicalTrials.gov/show/NCT01379456 University of Science and Technology; Trondheim kommune, enhet for fysioterapi; Norsk kvinners sanitetsforening Adt Jun-10 Jun-14 University http://ClinicalTrials.gov/show/NCT01427036 Sen Hospital, Tours Adt Nov-08 Dec-13 Mount Sinai http://ClinicalTrials.gov/show/NCT00749489 Sen School of Medicine; National Institute on Aging (NIA) Sen Apr-08 Apr-13 Norwegian http://ClinicalTrials.gov/show/NCT00667914 University of Science and Technology Adt Jan-11 Feb-13 University http://ClinicalTrials.gov/show/NCT01219712 Sen Hospital, Linkoeping; University Hospital Orebro; Ryhov County Hospital Adt Dec-08 Dec-12 St. Olavs http://ClinicalTrials.gov/show/NCT00626470 Sen Hospital Blood Loss and Complications of Internal Fixation of Femoral Neck Fractures in Patients Treated With Clopidogrel Non-randomized, parallel assignment, safety/efficacy study NCT00749710 Identification of the Microcirculation of the Caput Femoris After Fracture of the Femoral Neck Prospective, case-only study NCT01483404 Randomised trial of a blood transfusion policy after fracture of the proximal femur (hip fracture) RCT ISRCTN61328173 Optimal Positioning of Local Anaesthetic in Femoral Nerve Block Prior to Hip Surgery RCT, safety/efficacy study NCT01527812 Haemodynamic protocols in traumatology RCT ISRCTN66123742 The Effect of Loss of Offset After Pertrochanteric Fracture Treated With a Intramedullary Nail Cross-sectional, cohort study NCT01344785 The Warwick Hip Trauma Study RCT ISRCTN49197425 Procedure: clopidogrel; Procedure: no antiaggregant therapy Femoral Neck Fractures; Pertrochanteric Fractures; Antiaggregant Therapy Not yet 100 Rec Adt Sep-08 Dec-12 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT00749710 Procedure: Measurement with O2c Microcirculation of the Caput Femoris Not yet Rec 30 Adt Jun-12 Nov-12 RWTH Aachen Sen University http://ClinicalTrials.gov/show/NCT01483404 Oral iron Fracture of the supplements; Blood proximal femur (hip transfusion fracture) Active N/K Adt Aug-02 May-12 Department of Sen Health (UK) http://www.controlledtrials.com/ISRCTN61328173 Procedure: Femoral Fractured Neck of nerve block Femur Comp 60 Adt Feb-10 Feb-12 Cork University http://ClinicalTrials.gov/show/NCT01527812 Sen Hospital Targeted-volume Hemiarthroplasty of application guided by femoral neck oesophageal fractures Doppler; Postoperative directives versus conventional volume application Procedure: Intertrochanteric Intramedullary nailing Fractures Comp 40 Adt Jun-08 Dec-11 Charité http://www.controlledSen University trials.com/ISRCTN66123742 Medicine Berlin, Germany Rec 100 Adt Apr-10 Nov-11 Danderyd Sen Hospital http://ClinicalTrials.gov/show/NCT01344785 Fixed-angle screw Intracapsular and plate fixation; fractures of the Standard of care proximal femur fixation + placebo injection; Standard of care fixation + PRP injection Comp 225 Sen Aug-09 Aug-11 University of Warwick (UK) http://www.controlledtrials.com/ISRCTN49197425 157 Stroke Volume Optimisation in Patients With Hip Fracture Phase III: RCT, efficacy study NCT00444262 Procedure: hemodynamic optimisation guided using esophageal Doppler; Drug: VOLUVEN and others solute Procedure: Intertan Term 215 Sen Apr-07 Mar-11 Assistance http://ClinicalTrials.gov/show/NCT00444262 Publique Hôpitaux de Paris; Fresenius Kabi; GAMIDA Trochanteric and Comp Subtrochanteric Hip Fractures; Treatment With a New Nail or a Sliding Hip Screw 500 Adt Feb-08 Mar-10 Haukeland Sen University Hospital Hip Fracture Comp 150 Adt Jun-08 Jan-10 AO Clinical http://ClinicalTrials.gov/show/NCT00955565 Sen Investigation and Documentation Other: Strength training Hip Fracture Rec 120 Adt Sep-10 Jun-13 Lolland Sen Community, Denmark Other: Multidisciplinary management program Hip Fracture Rec 160 Adt Sep-09 Dec-12 Chinese http://ClinicalTrials.gov/show/NCT01382875 Sen University of Hong Kong; Queen Elizabeth Hospital, Hong Kong Other: Urine color Hip Fracture Rec 200 Adt Jan-11 Dec-12 University http://ClinicalTrials.gov/show/NCT01294930 Sen Hospital, Linkoeping; Vrinnevi Hospital Not yet Rec 60 Adt Feb-12 Aug-12 Meir Medical http://ClinicalTrials.gov/show/NCT01524718 Sen Center; Clalit Health Services A Prospective Randomised Multicenter Study Comparing the Sliding Hip Screw and the Intertan Nail in Trochanteric and Subtrochanteric Femoral Fractures RCT NCT00621088 Accuracy of Navigation in Procedure: Placement of Sacroiliac Screw Navigated; Phase IV: RCT, safety/efficacy Procedure: study Conventional NCT00955565 Other Training of Patients With Hip Fracture Phase II: RCT, efficacy study NCT01174589 The Comparison of Comprehensive Multi-disciplinary Program and Conventional Care Program on Fragility Fracture Elderly Phase III: Non-randomized, parallel assignement, efficacy study NCT01382875 Indicators of Operative and Postoperative Complications in Patients Operated for Hip Fracture Prospective, cohort study NCT01294930 Internal Fixation of Hip Fractures Using Intraoperative Simultaneous Two Axis View RCT, safety/efficacy study NCT01524718 Hip Fractures Radiation: Imaging Fracture Neck of with two X-ray image Femur intensifiers 158 http://ClinicalTrials.gov/show/NCT00621088 http://ClinicalTrials.gov/show/NCT01174589 HIP Fracture Accelerated Surgical Other: Accelerated Hip Fractures TreaTment And Care tracK (HIP surgical hip fracture ATTACK) Trial repair RCT NCT01344343 Jul-11 May-12 Population http://ClinicalTrials.gov/show/NCT01344343 Health Research Institute; Hamilton Health Sciences Corporation Strength Training After Hip Other: training of Hip Fracture Not yet 60 Adt Jan-11 Jul-11 Hvidovre http://ClinicalTrials.gov/show/NCT00848913 Fracture Surgery basic mobility; Other: Rec Sen University RCT training of kneeHospital; IMK NCT00848913 extension strength Fonden; Danish Physical Therapy Organization. Retrospective Study: Hip Fractures Other: HBA1C Type 2 Diabetes; Hip Comp 1162 Child Apr-11 Jun-11 Changi General http://ClinicalTrials.gov/show/NCT01379690 in Diabetic Patients Fractures Adt Hospital Retrospective, case control Sen study NCT01379690 Observation and Progressive Other: Strength Hip fracture Active, 150 Adt Jun-07 Dec-10 Oslo University http://ClinicalTrials.gov/show/NCT01129219 Strength Training After Hip training NR Sen Hospital; Fracture Diakonhjemmet RCT Hospital NCT01129219 Evaluation of home rehabilitation Multidisciplinary Hip fracture Comp 200 Sen Aug-08 Aug-10 Umeå University http://www.controlledfor hip fracture patients home rehabilitation; (Sweden) trials.com/ISRCTN15738119 RCT Conventional ISRCTN15738119 multidisciplinary rehabilitation at hospital Effect of a Medical Food Other: Medical Food Hip Fracture Comp 127 Adt Nov-09 Sep-10 Abbott Nutrition http://ClinicalTrials.gov/show/NCT01011608 Supplement in Hospitalized Supplement; Other: Sen Patients Recovering From Surgery standard hospital Phase III: RCT, efficacy study food NCT01011608 Miscellaneous observational studies Troponin T Elevation in Patient Undergoing Hip Fracture Surgery Prospective, cohort study NCT01352754 Hip Fracture Rec 50 Adt Sen Rec 100 Adt Apr-11 Apr-14 Hadassah Sen Medical Organization 159 http://ClinicalTrials.gov/show/NCT01352754 Rivaroxaban Safety Profile in the Prophylaxis of Venous Thromboembolism After Hip Fracture Surgery Prospective, case-only study NCT01509118 Improving Quality of Care for HipFracture Patients: Studies on Fasttrack Surgery Prospective, cohort study NCT01487772 Validation of Nexfin Cardiac Output in Elderly Patients With Hip Fracture Prospective, cohort study NCT01474824 Open Fracture of Hip Rec 500 Adt Sen Jul-11 Sep-13 Phramonghttp://ClinicalTrials.gov/show/NCT01509118 kutklao College of Medicine and Hospital (Thailand) Hip Fractures Rec 1300 Child Apr-10 Apr-13 Danderyd Adt Hospital Sen Hip Fractures; Anesthesia Not yet Rec 24 Dynamic Internal Fixation of Femoral Neck Fractures Prospective, cohort study NCT00779948 INTUIT Hip Fracture Outcome Study Prospective, cohort study NCT00595634 Bipolar H.A Versus Trochanteric Antegrade Nail for Treatment of Displaced Subcapital Femoral Fractures Retrospective, case control study NCT01181037 Bisphosphonate Users Radiographic Characteristics of the Hip (BURCH) Study Prospective study NCT01360099 Femoral Neck Fracture Rec 150 Unstable Intertrochanteric Hip Fractures Rec Displaced Subcapital Femoral Fracture Osteoporosis; Bone Diseases, Metabolic; Hip Fractures http://ClinicalTrials.gov/show/NCT01487772 Sen Jan-12 Jan-13 University of Nottingham; Nottingham University Hospitals NHS Trust; Brighton and Sussex University Hospitals NHS Trust Adt Dec-08 Dec-12 Aesculap AG Sen http://ClinicalTrials.gov/show/NCT01474824 125 Adt Jan-08 Dec-12 Smith & Sen Nephew, Inc. http://ClinicalTrials.gov/show/NCT00595634 Rec 200 Adt Jun-10 Apr-12 Meir Medical Sen Center http://ClinicalTrials.gov/show/NCT01181037 Rec 900 Adt May-11 Jan-12 National Institute http://ClinicalTrials.gov/show/NCT01360099 Sen of Arthritis and Musculoskeletal and Skin Diseases 160 http://ClinicalTrials.gov/show/NCT00779948 Waiting Time to Operation for Hipfracture Patients Retrospective, cohort study NCT01488812 Epidemiology of Aeromedical Evacuation Retrospective, cohort study NCT01071382 Timing of Orthopaedic Surgery in the Multiply-injured Patient: Development of a Protocol for Early Appropriate Care Prospective study NCT00888160 Economic Aspects Associated With the Implementation of an Orthogeriatric Setting in a General Hospital Retrospective, cohort study NCT00860132 Hip-fracture Comp Apoplexy; Femoral Comp Neck Fracture; Myocardial Infarction; Subarachnoid Hemorrhage; Polytrauma Unstable Pelvic Ring Rec Fracture; Unstable Acetabulum Fracture; Femur Fracture Hip Fracture 576 Child Jun-10 Dec-10 Danderyd Adt Hospital Sen http://ClinicalTrials.gov/show/NCT01488812 504 Child Feb-10 Feb-10 Ruhr University http://ClinicalTrials.gov/show/NCT01071382 Adt of Bochum; Sen Workers' Samaritan Federation Germany Child Sep-10 Apr-09 MetroHealth Adt Medical Center Sen http://ClinicalTrials.gov/show/NCT00888160 Not yet 2000 Adt May-09 Mar-09 Sheba Medical Rec Sen Center http://ClinicalTrials.gov/show/NCT00860132 Recruit n URL Active 60 A8C: ARTHROPLASTY Title Interventions Conditions Phases: trial design (control) CT ID Behavioural A pilot randomised controlled trial Pre-surgery home Primary THR of occupational therapy to optimise based occupational recovery for patients undergoing intervention; Jospital primary total hip replacement for based usual care osteoarthritis RCT ISRCTN38381590 161 Age Start (Grp) Date End Sponsors Date Adt Feb-12 Jan-13 University of Sen Birmingham (UK) http://www.controlledtrials.com/ISRCTN38381590 Comparison of Ways to Prepare Patients for Decisions About Joint Replacement Surgery Phase III: RCT NCT00911638 Device Cementless New Alumina-zirconia Ceramic Bearing Total Hip Arthroplasty (THA) in Asian Patients Single group assignment, safety/efficacy study NCT00935519 A Multi-centre Study to Assess the Long-term Performance of the Silent Hip™ in Primary Total Hip Replacement Surgery Phase IV: Single group assignment, safety/efficacy study NCT01383824 Zimmer Continuum Metal on Polyethylene (MoP) PostMarket Clinical Followup (PMCF) Study Prospective study NCT01307384 Behavioral: Patient decision aid and referral onward.; Behavioral: Patient education and referral onward Osteoarthritis; Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Device: 4th generation ceramic bearing composite ceramic bearing Arthroplasty, Replacement, Hip Active, NR 340 Child May-08 Jan-12 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00911638 Adt Research Sen Institute (Canada) Rec 310 Child May-09 Dec-30 Seoul National Adt University Sen Bundang Hospital http://ClinicalTrials.gov/show/NCT00935519 Device: Silent™ Hip Primary Arthritis; Secondary Arthritis Rec 500 Child Jan-11 Jul-27 DePuy Adt International http://ClinicalTrials.gov/show/NCT01383824 Device: Continuum(R) Metal on Polyethylene Acetabular System Rec 300 Adt Mar-11 Dec-24 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT01307384 Rec 150 Adt Jan-11 Nov-22 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01247038 Rec 125 Adt Jun-08 Jul-22 Exactech Sen http://ClinicalTrials.gov/show/NCT00715143 Patients Receiving Primary Hip Arthroplasty Using the Continuum Metal on Polyethylene Acetabular System A Multicentre Trial to Compare Device: Ceramic on Arthroplasty, Two Articulating Bearing Surfaces metal articulating Replacement, Hip as Used in Cementless Primary bearing surface Hip Arthroplasty Phase IV: RCT, safety/efficacy study NCT01247038 Post Approval Study: NOVATION Device: Novation Total Hip Ceramic Articulation Hip System Ceramic Replacement (NonPhase IV: Single group inflammatory) assignment, safety/efficacy study NCT00715143 162 CoMplete™ Acetabular Hip Device: Total hip System replacement Phase IV: Single group assignment, safety/efficacy study NCT01543230 A Study on M2a Magnum Total Hip Device: Metal-onArthroplasty Metal Articulation; RCT, safety/efficacy study Device: Metal-onNCT01010763 Metal Acetabular System A Study to Assess the Long-term Device: SmartSet® Performance of SmartSet® HV HV bone cement; and SmartSet® GHV Bone Device: SmartSet® Cements in Primary Total Hip GHV bone cement Replacement Phase IV: RCT, safety/efficacy study NCT00872066 A randomised, prospective, single blind study comparing a standard metal on polyethylene cemented socket in primary hip replacement versus an uncemented ceramic on ceramic bearing socket in patients under 65 years old RCT ISRCTN53483743 Joint Disease Invite 250 Adt Feb-12 Feb-22 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT01543230 Active, NR 184 Adt Nov-09 Dec-21 Biomet, Inc.; Sen Biomet Japan, Inc. http://ClinicalTrials.gov/show/NCT01010763 Rheumatoid Arthritis; Active, Osteoarthritis; PostNR traumatic Arthritis; Collagen Disorders; Avascular Necrosis; Traumatic Femoral Fractures; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis Uncemented ceramic Hip replacement Active on ceramic bearing; cemented socket with a metal on polyethylene 243 Adt Mar-06 Nov-21 DePuy Sen International http://ClinicalTrials.gov/show/NCT00872066 322 Adt Mar-05 Mar-20 Department of Health (UK) http://www.controlledtrials.com/ISRCTN53483743 Degenerative Joint Disease; Avascular Necrosis 163 A Multi-centre Study to Assess the Device: Summit Long-term Performance of the Tapered Hip System Summit™ Hip in Primary Total Hip Replacement Phase IV: Single group assignment, safety/efficacy study NCT00208390 ArCom® and ArComXL® Polyethylene Data Collection Prospective study NCT00565786 Trident® Tritanium™ Acetabular Shell Revision Study Single group assignment NCT00535626 An Electronic Data Capture Study to Assess the Long-term Performance of the DePuy PROXIMA™ Hip in Primary Total Hip Replacement Phase IV: Single group assignment, safety/efficacy study NCT01134445 Multi-Centre Study to Assess the Long-term Performance of the DePuy ASR™ System in Resurfacing and Primary Total Hip Replacement Phase IV: Non-randomized, parallel assignment, safety/efficacy study NCT00872547 Adt Mar-03 Dec-18 DePuy Sen International http://ClinicalTrials.gov/show/NCT00208390 150 Child Jul-04 Mar-17 Biomet Adt Orthopedics, Sen LLC http://ClinicalTrials.gov/show/NCT00565786 Active, NR 244 Adt Nov-06 Dec-16 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00535626 Rec 300 Adt Feb-10 Dec-15 DePuy Sen International http://ClinicalTrials.gov/show/NCT01134445 624 Adt Sep-06 Jun-15 DePuy International http://ClinicalTrials.gov/show/NCT00872547 Rheumatoid Arthritis; Active, Osteoarthritis; PostNR traumatic Arthritis; Collagen Disorders; Avascular Necrosis; Traumatic Femoral Fractures; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis Arthroplasty, Active, Replacement, Hip NR 293 Device: ArCom® Polyethylene; Device: ArComXL® Polyethylene Device: Trident® Arthroplasty, Tritanium™ Replacement, Hip Acetabular Shell Device: DePuy Proxima™ Hip Rheumatoid Arthritis; Osteoarthritis; Posttraumatic Arthritis; Avascular Necrosis; Traumatic Femoral Fractures; Congenital Hip Dysplasia Device: DePuy ASR™ Hip System; Device: DePuy ASR™ XL Head / ASR™ Acetabular Cup System Rheumatoid Arthritis; Active, Osteoarthritis; PostNR traumatic Arthritis; Collagen Disorders; Avascular Necrosis; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis 164 A Two Centre Study to Assess the Device: Pinnacle Long-term Performance of the Acetabular Cup Pinnacle™ Cup With a Metal-on- System Metal Bearing in Primary Total Hip Replacement Phase IV: Single group assignment, safety/efficacy study NCT00208364 Rheumatoid Arthritis; Active, Osteoarthritis; PostNR traumatic Arthritis; Collagen Disorders; Avascular Necrosis; Traumatic Femoral Fractures; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis Total Hip Active Arthroplasty Periprosthetic bone mineral Metha short stem density (BMD) around two different (monoblock with stems in total hip arthroplasty 130° CCD angle and Observational, cohort study 0° ante-, retrotorsion) ISRCTN54967983 or the Bicontact stem (AESCULAP AG, Tuttlingen, Germany) A Two Centre Study to Assess the Device: C-Stem™ Rheumatoid Arthritis; Term Stability and Long-term AMT Femoral Osteoarthritis; PostPerformance of the C-Stem™ AMT Component traumatic Arthritis; in a Total Primary Hip (standard and high Collagen Disorders; Replacement off-set variants) Avascular Necrosis; Phase IV: Single group Traumatic Femoral assignment, safety/efficacy Fractures; Nonunion study of Femoral NCT00872573 Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis. Omnifit Hydroxylapatite (HA) Hip Device: Omnifit HA Arthroplasty, Active, Outcomes Study Hip Stem Replacement, Hip NR Prospective, cohort study NCT00958347 Randomised trial of hip fractures Hemiarthroplasty Hip fracture; Hip Active treated with two different types of method 1; Replacement hip replacements hemiarthroplasty RCT method 2 ISRCTN04635269 200 Adt Apr-04 Mar-15 DePuy Sen International http://ClinicalTrials.gov/show/NCT00208364 50 Adt Jun-06 Dec-14 German Sen Research Council http://www.controlledtrials.com/ISRCTN54967983 50 Adt Sen 262 Adt Oct-87 Dec-14 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00958347 600 Adt Nov-06 Nov-14 Department of Sen Health (UK) http://www.controlledtrials.com/ISRCTN04635269 165 Jul-06 Dec-14 DePuy International http://ClinicalTrials.gov/show/NCT00872573 Accolade TMZF Hip Stem Study Single group assignment NCT00957658 RCT of Ceramic Bearing Primary Total Hip Arthroplasty Phase IV: RCT, safety/efficacy study NCT01522014 Device: Accolade TMZF Stem Arthroplasty, Replacement, Hip Active, NR 249 Adt Mar-06 Jun-14 Stryker Sen Orthopaedics Device: Secure-Fit™ Total Hip Active, arc-deposited Replacement NR Hydroxylapatite (HA) shell - surface ceramic and an Alumina Bearing Couple (ABC) ceramic insert and Ceramic C-taper head; Device: Secure-Fit™ arcdeposited hydroxylapatite shell, a Crossfire® insert and a Ceramic Ctaper head Encore Revelation Hip Stem Device: Revelation Osteoarthritis, Hip; Invite Prospective, cohort study Hip Stem Complications; NCT01514318 (Revelation) Arthroplasty A Multi-centre Study to Assess the Device: DePuy Rheumatoid Arthritis; Active, Long-term Performance of the Proxima™ Hip Osteoarthritis; PostNR DePuy PROXIMA™ Hip in Primary traumatic Arthritis; Total Hip Replacement Avascular Necrosis; Phase IV: Single group Traumatic Femoral assignment, safety/efficacy Fractures; study Congenital Hip NCT00208455 Dysplasia. Ceramic-on-Ceramic Total Hip Device: THA with Hip Arthrosis Rec Arthroplasty and Squeaking: ABG II / Trident; Influence of Component Design Device: THA with RCT CLS / Trilogy NCT01420900 The Efficacy and Cost Analysis of Device: Hemovac Total Joint Rec Arthroplasty; Hip, Reinfusion Drains Versus drain; Device: Knee Tranexamic Acid in Total Joint OrthoPAT drain; Arthroplasty Drug: Tranexamic Phase IV: RCT, efficacy study acid NCT01514474 92 Adt Nov-97 Jun-14 University of http://ClinicalTrials.gov/show/NCT01522014 Alberta; Stryker Canada 39 Adt Feb-12 Feb-14 Encore Medical, http://ClinicalTrials.gov/show/NCT01514318 Sen L.P. 184 Adt Mar-05 Nov-13 DePuy Sen International http://ClinicalTrials.gov/show/NCT00208455 204 Adt Sep-11 Oct-13 Vejle Hospital http://ClinicalTrials.gov/show/NCT01420900 234 Adt Jan-12 Jun-13 OrthoCarolina Sen Research Institute, Inc. http://ClinicalTrials.gov/show/NCT01514474 166 http://ClinicalTrials.gov/show/NCT00957658 Post-approval Study of the DURALOC® Option Ceramic-onCeramic Hip Prosthesis System Phase IV: Single group assignment, safety/efficacy study NCT00546598 Efficacy of a New Resurfacing Hip Prosthesis Phase III: RCT, safety/efficacy study NCT00391937 A Single Centre Study to Assess the Long-term Performance of the Pinnacle™ Cup With a Ceramicon-ceramic Bearing in Primary Total Hip Replacement Phase IV: Single group assignment, safety/efficacy study NCT00872222 Prediction of Pain in Total Hip Arthroplasty Single group assignment NCT01324375 Device: Total hip replacement/arthropl asty; Device: Hip replacement/arthropl asty Device: Articular Surface Replacement (ASR) hip prosthesis Device: Pinnacle™ Acetabular System Non-inflammatory Joint Disease; Osteoarthritis; Avascular Necrosis; Congenital Hip Dysplasia; Posttraumatic Arthritis Osteoarthritis, Hip Active, NR 250 Adt Jan-06 May-13 DePuy Sen Orthopaedics Rec 150 Adt Rheumatoid Arthritis; Term Osteoarthritis; Posttraumatic Arthritis; Collagen Disorders; Avascular Necrosis; Traumatic Femoral Fractures; Nonunion of Femoral Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis Pain, Postoperative Rec 200 Adt Nov-06 Jan-13 DePuy Sen International http://ClinicalTrials.gov/show/NCT00872222 60 Adt Mar-11 Dec-12 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01324375 345 Adt Sen Device: heat pain test (Modular Sensory Analyzer, Somedic AB, Horby, Sweden). Safety and Effectiveness Study of Device: Reflection Osteoarthritis the Reflection Ceramic Acetabular Ceramic-Ceramic System Total Hip Phase IV: Non-randomized, Replacement; parallel assignment, Device: Reflection safety/efficacy study FSO V Total Hip NCT00663351 Replacement Active, NR 167 http://ClinicalTrials.gov/show/NCT00546598 Oct-06 Mar-13 Erasmus http://ClinicalTrials.gov/show/NCT00391937 Medical Center; Johnson & Johnson 38322 Dec-12 Smith & Nephew, Inc. http://ClinicalTrials.gov/show/NCT00663351 Analysis of Crosslinked and Conventional Polyethylene Explants Retrospective, cohort study NCT01484002 Device: Total hip arthroplasty Osteoarthritis Invite 60 Unipolar or Bipolar Device: Unipolar hip Hemiarthroplasty in the Treatment hemiarthroplasty; of Displaced Femoral Neck Device: Bipolar hip Fractures. hemiarthroplasty RCT, efficacy study NCT00746876 A Prospective Study to Evaluate Device: Vitagel the Effectiveness of a Haemostatic Agent in Primary Unilateral Total Hip Arthroplasty Phase IV: RCT, efficacy study NCT01285024 Clinical Study Evaluating an Device: Acetabular Acetabular Cup System After Total cup Hip Replacement Phase IV: Non-randomized, parallel assignment, safety/efficacy study NCT00306930 A Five-Year Metal-on-Metal Device: Metal-onRetrospective Clinical Study metal primary total Retrospective, cohort study hip arthroplasty NCT01481896 (DePuy ) Hip Fractures Active, NR 30 Rec 110 Osteoarthritis Invite 131 RCT Comparing Ion Levels and Device: A Class Clinical Outcomes of A-Class BFH BFH; Device: Metal to Metal on Polyethylene Total Hip on Polyethylene Replacement Phase IV: RCT NCT00911599 Hip Joint; Osteoarthritis; Arthroplasty Rec 60 Arthritis Adt Dec-11 Dec-12 Anderson http://ClinicalTrials.gov/show/NCT01484002 Sen Orthopaedic Research Institute; Orthopaedic Biomechanics and Biomaterials Laboratory at Massachusetts General Hospital; DePuy Orthopaedics Sen Sep-09 Dec-12 Sykehuset Asker http://ClinicalTrials.gov/show/NCT00746876 og Baerum; Ullevaal University Hospital Adt Dec-10 Oct-12 The Cleveland http://ClinicalTrials.gov/show/NCT01285024 Sen Clinic; Orthovita Osteoarthritis; Active, 1500 Child Oct-00 Jun-12 DePuy Rheumatoid Arthritis; NR Adt Orthopaedics Arthritis; Avascular Sen Necrosis; Acute Fracture 168 http://ClinicalTrials.gov/show/NCT00306930 Adt Dec-11 Jun-12 Anderson http://ClinicalTrials.gov/show/NCT01481896 Sen Orthopaedic Research Institute; DePuy Orthopaedics Adt Aug-06 May-12 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00911599 Sen Research Institute; Wright Medical Technology Restoration® Modular Revision Device: Restoration Arthroplasty, Hip System Post Market Study Modular Revision Hip Replacement, Hip Single group assignment System NCT00962013 Comparing Total Hip Arthroplasty Device: Total hip Hip Fractures; and Hemi-Arthroplasty on Revision arthroplasty; Device: Femoral Neck Surgery and Quality of Life in Hemi-arthroplasty Fractures Adults With Displaced Hip Fractures (The HEALTH Study) Phase II: RCT, efficacy study NCT00556842 A Comparison of Two Total Hip Device: ReCap, Hip Osteoarthrosis Replacements: Hip Resurfacing resurfacing system, System Versus MalloryBiomet Head/Exeter Phase IV: RCT, safety/efficacy study NCT00116948 Trident X3 Polyethylene Insert Device: Trident X3 Arthroplasty, Study Polyethylene Insert Replacement, Hip Single group assignment NCT00958191 Study Comparing Marathon Device: Total Hip Osteoarthritis; Polyethylene and Enduron Replacement Arthritis; Joint Polyethylene Acetabular Liners Diseases; Used in Total Hip Arthroplasty Musculoskeletal RCT Diseases; NCT01121146 Rheumatic Diseases Metal-metal Articulations Versus Device: articular Osteoarthritis, Hip Standard 28 mm Cementless Total surface replacement Hip Arthroplasty ASR, DePuy; Device: Phase II: RCT, efficacy study ReCap/Magnum NCT01113762 modular head, Biomet; Device: Bimetric stem, mallory/head cup, 28 mm ceramic head, Biomet; Device: 28 mm CrCo head, Trilogy CH cup, VerSys Fiber stem,Zimmer) Active, NR 144 Adt Jan-04 Apr-12 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00962013 Rec 306 Adt Mar-09 Mar-12 Boston Sen University (US) http://ClinicalTrials.gov/show/NCT00556842 Active, NR 50 Adt http://ClinicalTrials.gov/show/NCT00116948 Active, NR 240 Adt May-05 Jan-12 Stryker Sen Orthopaedics Active, NR 236 Child Dec-98 Dec-11 Anderson http://ClinicalTrials.gov/show/NCT01121146 Adt Orthopaedic Sen Research Institute; DePuy Orthopaedics Active, NR 71 169 Jan-05 Jan-12 University of Aarhus (Denmark) http://ClinicalTrials.gov/show/NCT00958191 Adt Feb-07 Nov-11 University of http://ClinicalTrials.gov/show/NCT01113762 Southern Denmark; Ministry of the Interior and Health, Denmark; Region Sealand; Biomet, Inc.; DePuy Orthopaedics; ALS Laboratory Group Study to Assess the Stability, Device: DePuy Osteoarthritis Efficacy and Safety of the Silent™ Silent™ Hip femoral Hip Prosthesis in Primary Total Hip prosthesis Replacement Phase III: Single group assignment, safety/efficacy study NCT00894140 Scan Hip Evaluation Device: Metal on Hip Arthroplasty Single group assignment metal hip NCT01349179 arthroplasty operated on 2002 A Multi-centre Study to Assess the Device: Pinnacle Rheumatoid Arthritis; Long-term Performance of the Acetabular System Osteoarthritis; PostPinnacle™ Cup With a traumatic Arthritis; Polyethylene-on-metal Bearing in Collagen Disorders; Primary Total Hip Replacement Avascular Necrosis; Phase IV: Single group Traumatic Femoral assignment, safety/efficacy Fractures; Nonunion study of Femoral NCT00208429 Fractures; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis. A Randomised Single Centre Device: Smartset HV Osteoarthritis; PostStudy to Compare the Long-term Bone Cement; traumatic Arthritis; Performance of SmartSet® HV Device: Palacos R Avascular Necrosis and Palacos® R Bone Cements in Primary Total Hip Replacement Phase IV: RCT, safety/efficacy study NCT00208403 Metal on Metal Versus Ceramic on Device: Total Hip Joint Diseases Metal Hip Replacement Replacement; Phase IV: RCT, safety/efficacy Device: Total hip study replacement NCT00208494 Active, NR 41 Adt Jan-03 Sep-11 DePuy http://ClinicalTrials.gov/show/NCT00894140 International; Johnson and Johnson Medical Comp 100 Child Dec-10 Sep-11 University Adt Hospital, Sen ClermontFerrand Sep-11 DePuy Wdrwn 200 Adt Sen International http://ClinicalTrials.gov/show/NCT01349179 http://ClinicalTrials.gov/show/NCT00208429 Active, NR 36 Adt Oct-02 Sep-11 DePuy Sen International http://ClinicalTrials.gov/show/NCT00208403 Comp 390 Adt Aug-05 Jun-11 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00208494 170 Bimetric-10: Investigation of Patients Who Have Underwent Total Hip Arthroplasty With a Cemented Bi-Metric Stem Retrospective, cohort study NCT00192699 A Short Metaphyseal Fitting Total Hip Arthroplasty in Young and Elderly Patients Phase IV: RCT NCT01345097 Use of Knotless Suture for Closure of Total Hip and Knee Arthroplasties RCT, efficacy study NCT00834483 28 mm Ceramic-on-Ceramic Acetabular Cup Total Hip Replacement Study Phase III: RCT, safety/efficacy study NCT00208507 ABC/Trident Ceramic Post Approval Study RCT, safety/efficacy study NCT00960206 Prevena™ Incision Management System Over Primarily Closed Hip and Knee Incisions in Patients Immediately Post Total Hip and Knee Arthroplasty Phase IV: Single group assignment NCT01380665 A Clinical Investigation of Recovery Following Hip Resurfacing or Total Hip Arthroplasty Non-randomized, parallel assignment NCT00585988 Device: Bimetric femoral stem Osteoarthrosis Comp 100 Adt Jan-04 Apr-11 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00192699 Device: Total Hip Arthroplasty Osteonecrosis; Osteoarthritis Comp 200 Adt May-04 Mar-11 Ewha Womans Sen University http://ClinicalTrials.gov/show/NCT01345097 Device: Knotless Primary Knee Active, suture for wound Arthroplasty; Primary NR closure; Device: Hip Arthroplasty Layered traditional wound closure (monocryl) Device: 28 mm Joint Diseases Comp ceramic head on ceramic acetabular liner.; Device: 28 mm ceramic head on polyethylene liner Device: Ceramic Arthroplasty, Comp Post Approval Replacement, Hip 200 Adt Feb-09 Jan-11 Rush University http://ClinicalTrials.gov/show/NCT00834483 Sen Medical Center 264 Adt Apr-03 Dec-10 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00208507 518 Adt Mar-03 Oct-10 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00960206 Device: Prevena Linear or Emi-linear Incisional Incisions; Total Hip Management System Arthroplasty; Total Knee Arthroplasty 100 Adt Oct-09 Oct-10 KCI USA, Inc. Sen http://ClinicalTrials.gov/show/NCT01380665 0 Adt Jun-07 Sep-10 Biomet Sen Orthopedics, LLC http://ClinicalTrials.gov/show/NCT00585988 Device: Hip Resurfacing System; Device: M2aMagnum™ Large Metal Articulation Term Osteoarthritis; Wdrwn Rheumatoid Arthritis; Arthritis; Traumatic Arthritis 171 Evaluation of the Efficacy of the Device: Aquamantys; Blood Loss Comp Bipolar Sealer Aquamantys 6.0 in Procedure: Standard Patients Undergoing Total Hip Electrocautery Arthroplasty Phase IV: RCT, efficacy study NCT01448967 Comparison in Need for Bank Device: Sangvia® Arthroplasty, Comp Blood Between Patients System Replacement, Hip; Undergoing Total Hip Surgery That Blood Transfusion; Either Receive Their Own Blood Blood Transfusion, Back or Not Autologous RCT, efficacy study NCT00822588 Total Hip Replacement With the Device: Answer® hip Osteoarthritis, Hip; Term Answer® Hip Stem and stem; Device: Traumatic Arthritis of Ranawat/Burnstein® Shell Using Answer® hip stem Hip Simplex® or Palacos® Bone Cement Non-randomized, parallel assignment NCT00588861 A Comparison of a Resurfacing Device: Hip Osteoarthritis Comp Hip System to Standard Total Hip Resurfacing System Arthroplasty Phase IV: Single group assignment, safety/efficacy study NCT00253877 Drugs including biologics Intravenous Ferric Carboxymaltose Drug: Ferinject 50 (Ferinject) in Patients Undergoing mg/ml; Drug: NaCl Orthopaedic Surgery 0.9% Phase IV: RCT, safety/efficacy study NCT01345968 Effect of Denosumab on Drug: Denosumab; Inflammatory Osteolytic Lesion Other: Placebo Activity in Total Hip Arthroplasty Phase II: RCT NCT01358669 Anemia; Knee Replacement; Hip Replacement Revision Surgery of Total Hip Arthroplasty 140 Adt Nov-06 Jun-10 Salient Surgical http://ClinicalTrials.gov/show/NCT01448967 Sen Technologies; The Cleveland Clinic 227 Adt May-09 Jun-10 Astra Tech AB Sen http://ClinicalTrials.gov/show/NCT00822588 400 Adt Sep-02 May-10 Biomet Sen Orthopedics, LLC http://ClinicalTrials.gov/show/NCT00588861 200 Adt Sen Rec 140 Adt Jun-11 Oct-15 University http://ClinicalTrials.gov/show/NCT01345968 Sen Hospital Muenster; Vifor Pharma Not yet Rec 30 Adt Jan-12 Jan-15 Sheffield http://ClinicalTrials.gov/show/NCT01358669 Sen Teaching Hospitals NHS Foundation Trust; Amgen; NIHR Musculoskeletal BRU 172 Jul-03 May-10 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00253877 Research Institute; Wright Medical Technology Effect of Zoledronic Acid on Drug: Zoledronic acid Osteoporosis Femoral Bone Loss Following Total Hip Arthroplasty Phase IV: RCT, safety/efficacy study NCT01267279 Rifampin Combination Therapy Drug: RifampinProsthesis-related Versus Monotherapy in Early combination therapy; Infections; Staphylococcal Infections After Drug: Monotherapy Staphylococcal Total Hip and Knee Arthroplasty Infections Phase IV: RCT, efficacy study NCT00423982 Hydroxyethyl Starch and Renal Drug: Voluven 60 Arthroplasty, Function After Hip Replacement mg/ml; Drug: Sodium Replacement, Hip Surgery Chloride 9 mg/ml Phase IV: RCT, safety study NCT01486576 Clinical Trial of Gabapentin to Drug: Gabapentin Postoperative Pain; spine, hip or knee Improve Postoperative Pain in replacement. Surgical Patients Phase III: RCT, safety/efficacy study NCT00221338 Safety and Efficacy of IM Injections Biological: PLX-PAD Total Hip of PLX-PAD for the Regeneration low dose; Biological: Arthroplasty; Muscle of Injured Gluteal Musculature PLX-PAD high dose; Injury After Total Hip Arthroplasty Biological: Placebo Phase I/II: RCT, safety/efficacy study NCT01525667 A comparison of the need for bupivicaine via the Primary hip opiate pain relief medication after pain pump device arthroplasty elective hip replacement surgery into the tissues between patients given Local surrounding the new Anaesthetic Infiltration to the new joint; placebo via the joint and then an infusion of either pain pump device local anaesthetic or placebo into the tissues around the new joint surrounding the new RCT (placebo), efficacy study joint ISRCTN24271997 Active, NR Rec 66 Child Jan-05 Jan-15 Spokane Joint Adt Replacement Sen Center http://ClinicalTrials.gov/show/NCT01267279 100 Child Apr-06 Dec-14 Oslo University Adt Hospital Sen http://ClinicalTrials.gov/show/NCT00423982 Not yet Rec 40 Adt Dec-11 Dec-14 Holstebro Sen Hospital http://ClinicalTrials.gov/show/NCT01486576 Rec 312 Adt Aug-05 Sep-14 University of Sen California, San Francisco http://ClinicalTrials.gov/show/NCT00221338 Not yet Rec 18 Adt Apr-12 Dec-13 Pluristem Ltd. Sen http://ClinicalTrials.gov/show/NCT01525667 Active 70 Adt Oct-11 Oct-13 Leeds Teaching http://www.controlledSen Hospitals NHS trials.com/ISRCTN24271997 Trust (UK) 173 Psoas Compartment Block Versus Fascia Iliaca Block After Total Hip Arthroplasty RCT, efficacy study NCT01378949 Oxycodone Versus Intravenous Morphine for Postoperative Analgesia After Hip Surgery Phase IV: RCT, safety/efficacy study NCT01536301 Study To Investigate The Effectiveness Of Pregabalin For Management Of Patients Undergoing Total Hip Replacement Phase III: RCT, safety/efficacy study NCT00905437 A Study of LY2495655 in Older Patients Undergoing Elective Total Hip Replacement Phase II: RCT, safety/efficacy study NCT01369511 An international study to assess the effects of strontium ranelate in the reduction of bone loss around the metal implant, in patients with hip prosthesis RCT ISRCTN15928978 Treatment of Patients Undergoing Primary Unilateral Elective Total Knee or Hip Replacement With Dabigatran Etexilate Phase IV: RCT, pharmacokinetics/dynamics study NCT01184989 Drug: Bupivacaine; Drug: Morphine Pain Drug: Standard Care Arthroplasty, morphine Replacement, Hip hydrochloride; Drug: Oxycodone Not yet Rec 90 Not yet 246 Rec Adt Sep-11 Sep-13 Hillel Yaffe Sen Medical Center http://ClinicalTrials.gov/show/NCT01378949 Adt Mar-12 Sep-13 Centre http://ClinicalTrials.gov/show/NCT01536301 Sen Hospitalier Universitaire de Nīmes Drug: Placebo; Drug: Pain, Perioperative Pregabalin Rec 256 Adt Nov-09 Jun-13 Pfizer Sen http://ClinicalTrials.gov/show/NCT00905437 Drug: LY2495655; Drug: Placebo Total Hip Replacement Rec 340 Adt Sen http://ClinicalTrials.gov/show/NCT01369511 2g of strontium ranelate; placebo Total Hip Replacement Active 126 Adt May-11 Apr-13 Institut de http://www.controlledSen Recherche trials.com/ISRCTN15928978 Internationales Servier (France) Drug: Dabigatran etexilate Arthroplasty, Replacement, Knee; Venous Thromboembolism Rec 100 Adt Aug-10 Apr-13 Boehringer http://ClinicalTrials.gov/show/NCT01184989 Sen Ingelheim Pharmaceuticals 174 Jul-11 May-13 Eli Lilly and Company Daptomycin Use for Antimicrobial Drug: Daptomycin; Prophylaxis in Methicillin Resistant Drug: Vancomycin Staphylococcus Aureus (MRSA) Colonized Adult Patients Undergoing Primary Elective Hip or Knee Arthroplasty Phase IV: RCT, efficacy study NCT01196169 Study to Observe Safety of Xarelto Drug: Rivaroxaban in VTE Prophylaxis After Elective (Xarelto, BAY59TKR or THR 7939) Prospective, cohort study NCT01523418 Rotational Thromboelstometry Drug: Pentaspan, (ROTEM) change_colloid_total Hip voluven, volulyte Replacement Arthroplasty RCT NCT01512628 Russian Non-Interventional Study Drug: Rivaroxaban on Compliance of Venous (Xarelto, BAY59Thromboembolism (VTE) 7939) Prospective, case control study NCT01444586 Xarelto for VTE Prophylaxis After Drug: Rivaroxaban Hip or Knee Arthroplasty (Xarelto, BAY59Prospective, cohort study 7939); Drug: NCT00831714 Standard care treatment for VTE prophylaxis Effect of Spinal Ketorolac on Drug: ketorolac Mechanical Hypersensitivity After a tromethamine Total Hip Replacement opthalmic solution; Phase II: RCT, efficacy study Drug: placebo NCT00621530 Prophylaxis Against DVTs After Primary Hip and Knee Replacement Surgery RCT, safety/efficacy study NCT00767559 Staphylococcal Infections; Methicillin-resistant Staphylococcus Aureus Prophylaxis, Thromboembolism, Venous; Total Knee Replacement; Total Hip Replacement Avascular Necrosis of Hip; Total Hip Replacement Arthroplasty Rec 100 Not yet 500 Rec Rec 54 Adt Oct-10 Apr-13 Mountain Home http://ClinicalTrials.gov/show/NCT01196169 Sen Research & Education Corporation; East Tennessee State University; Cubist Pharmaceuticals Adt Jun-12 Apr-13 Bayer http://ClinicalTrials.gov/show/NCT01523418 Sen Adt Jan-12 Jan-13 Seoul National Sen University Bundang Hospital http://ClinicalTrials.gov/show/NCT01512628 Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Rec 2522 Adt Oct-11 Dec-12 Bayer Sen http://ClinicalTrials.gov/show/NCT01444586 Venous Thromboembolism Rec 15000 Adt http://ClinicalTrials.gov/show/NCT00831714 Hip Arthroplasty Drug: warfarin; Drug: Pulmonary Fondaparinux:; Drug: Embolism warfarin Feb-09 Nov-12 Bayer Sen Active, NR 100 Active, NR 330 175 Adt Mar-08 Oct-12 James C. http://ClinicalTrials.gov/show/NCT00621530 Sen Eisenach, M.D.; National Institute of General Medical Sciences (NIGMS) Adt Nov-08 Oct-12 The New http://ClinicalTrials.gov/show/NCT00767559 Sen England Baptist Hospital Low Dose Extended-release Drug: Extended Hip Arthroplasty Epidural and Lumbar Plexus Block Release Epidural Compared to Lumbar Plexus Block Morphine (EREM); for Total Hip Resurfacing Drug: Placebo RCT, efficacy study NCT00934661 Single IV Administration of TB-402 Drug: TB-402; Drug: Prophylaxis of for Prophylaxis of Venous Rivaroxaban; Drug: Venous Thromboembolic Events (VTE) TB-402 Thromboembolic After Total Hip Replacement Events Surgery Phase II: RCT, safety/efficacy study NCT01344954 Total Hip Arthroplasty: Multiple Drug: Ropivacaine; Pain, Postoperative Blocks by UltraSound Drug: Ropivacaine; RCT, efficacy study Device: Ultrasound; NCT01276925 Procedure: Peripheral nerve blockade; Drug: Saline; Procedure: Total hip arthroplasty; Drug: Bupivacaine Effect of Reversing Muscle Drug: Sugammadex; Neuromuscular Relaxation With Sugammadex Drug: neostigmine Blockade; Compared With Usual Care on and glycopyrrolate or Arthroplasty, Bleeding Risk in Patients on Blood atropine; Drug: Replacement, Hip; Thinners Undergoing Major Joint Placebo Arthroplasty, Surgery (P07038/MK-8616-059) Replacement, Knee; Phase III: RCT, safety study Blood Coagulation; NCT01422304 Antithrombotic Agents The Effect of Periarticular MultiDrug: periarticular Femoral Neck Drug Regimen on Pain After injection of multidrug Fracture Partial Hip Replacement regimen; Drug: none Phase IV: RCT, efficacy study of medication NCT01112436 preoperatively and intraoperatively Rec 60 Adt Rec 600 Adt Apr-11 Jul-12 ThromboGenics; http://ClinicalTrials.gov/show/NCT01344954 Sen BioInvent International AB Rec 81 Adt Aug-11 May-12 Bispebjerg Sen Hospital Rec 800 Adt Oct-11 May-12 Schering-Plough http://ClinicalTrials.gov/show/NCT01422304 Sen Rec 258 Child May-10 Apr-12 Chung-Ang Adt Univerisity Sen Hospital 176 Jan-10 Jul-12 Wake Forest http://ClinicalTrials.gov/show/NCT00934661 University; EKR Therapeutics, Inc http://ClinicalTrials.gov/show/NCT01276925 http://ClinicalTrials.gov/show/NCT01112436 Use of Etoricoxib Compared to Drug: Etoricoxib; Diclofenac in the Perioperative Drug: Diclofenac Treatment of Patients After Total Hip Arthroplasty Phase III: RCT, efficacy study NCT01229774 Prevention of Heterotopic Drug: Etoricoxib Ossification With Arcoxia After (Arcoxia) Total Hip Replacement Phase IV: Single group assignment, efficacy study NCT01022190 Evaluating the Effectiveness of 2 Drug: Duraprep Surgical Skin Preparation Methods Surgical Solution in Reducing Surgical Wound Drainage After Total Hip or Knee Replacement RCT, efficacy study NCT01097135 Postoperative Pain Relief Drug: LIA; Drug: I/T Following Total Hip Arthroplasty. A morphine Comparison Between Intrathecal Morphine (IM) and Local Infiltration Analgesia (LIA) Phase IV: RCT, safety/efficacy study NCT01281891 Topical Application of Tranexamic Drug: Tranexamic Acid Reduces Postoperative Blood Acid; Drug: normal Loss in Total Hip Arthroplasty saline RCT NCT01260818 Coxarthrosis; Arthroplasties Hip Replacement; Perioperative Blood Loss Rec 100 Adt Feb-11 Feb-12 University of Sen Regensburg; Merck http://ClinicalTrials.gov/show/NCT01229774 Osteochondritis; Ossification, Heterotopic Rec 42 Adt Dec-09 Jan-12 Radboud Sen University http://ClinicalTrials.gov/show/NCT01022190 Drainage Rec 600 Adt Mar-10 Dec-11 Rothman Sen Institute Orthopaedics; 3M http://ClinicalTrials.gov/show/NCT01097135 Primary Osteoarthritis Requiring Total Hip Replacement Rec 80 Adt Sep-09 Dec-11 University http://ClinicalTrials.gov/show/NCT01281891 Sen Hospital Orebro Hip Replacement; Postoperative Hemorrhage Rec 100 Pradaxa (Dabigatran Etexilate) VTE Prevention After Elective Total Hip or Knee Replacement Surgery Prospective, cohort study NCT01153698 Venous Thromboembolism; Arthroplasty, Replacement Term 167 Adt Dec-10 Dec-11 The First http://ClinicalTrials.gov/show/NCT01260818 Sen Affiliated Hospital, Guangzhou University of Traditional Chinese Medicine Adt Aug-10 Nov-11 Boehringer http://ClinicalTrials.gov/show/NCT01153698 Sen Ingelheim Pharmaceuticals Drug: dabigatran 177 Postoperative Pain Control After Hip Hemiarthroplasty: Intrathecal Morphine vs Periarticular Infiltration of Bupivacaine Phase IV: RCT, efficacy study NCT01219062 Use of Local Infiltration Analgesia Following Total Hip Arthroplasty Phase IV: RCT, efficacy study NCT01344395 Use of Local Analgesia With Epinephrine During Total Hip Arthroplasty (THA) Phase II: RCT, efficacy study NCT00980616 The Analgesic Efficacy of Periarticular Infiltration of Local Anaesthetic for Total Hip Replacement Phase IV: RCT, efficacy study NCT01312077 Extended Prophylaxis Comparing low molecular weight heparin (LMWH) to Aspirin in Total hip arthroplasty RCT ISRCTN11902170 Dabigatran Etexilate Compared With Enoxaparin in Prevention of Venous Thromboembolism (VTE) Following Total Hip Arthroplasty Phase III: RCT, safety/efficacy study NCT00657150 Morphine COnsumption in Joint Replacement Patients, With and Without GaBapentin Treatment, a RandomIzed ControlLEd Study RCT, efficacy study NCT00889148 Drug: Morphine or Femoral Neck 0.25 % Bupivacaine Fracture Rec 60 Adt Sep-10 Sep-11 Mahidol Sen University http://ClinicalTrials.gov/show/NCT01219062 Drug: ropivacaine Pain, Postoperative; and ketorolac; Drug: Pain Ketorolac Rec 80 http://ClinicalTrials.gov/show/NCT01344395 Drug: ropivacaine, physical serum and adrenalin Arthroplasty, Replacement, Hip Rec 150 Adt Mar-10 Sep-11 University of Sen Aarhus; Lundbeck Foundation Adt Sep-09 Sep-11 University Sen Hospital, ClermontFerrand Drug: Levobupivacaine; Drug: Intrathecal morphine Total Hip Arthroplasty Rec 50 Aspirin; Dalteparin; Placebo Elective total hip arthroplasty Comp 2222 Adt Sep-07 Mar-11 Dalhousie Sen University (Canada) Drug: Enoxaparin; Drug: Dabigatran etexilate Venous Thromboembolism Comp 2055 Adt Mar-08 Feb-11 Boehringer http://ClinicalTrials.gov/show/NCT00657150 Sen Ingelheim Pharmaceuticals Drug: Gabapentin; Other: Placebo Postoperative Pain; Total Hip Replacement Comp 103 178 http://ClinicalTrials.gov/show/NCT00980616 Adt Oct-10 Jun-11 Cork University http://ClinicalTrials.gov/show/NCT01312077 Sen Hospital http://www.controlledtrials.com/ISRCTN11902170 Adt Oct-07 Feb-11 Hamilton Health http://ClinicalTrials.gov/show/NCT00889148 Sen Sciences Corporation Dabigatran Etexilate in Extended Drug: dabigatran Venous Thromboembolism (VTE) etexilate; Drug: Prevention After Hip Replacement dabigatran etexilate; Surgery Drug: enoxaparin Phase III: RCT, efficacy study NCT00168818 Effects of Methylprednisolone After Drug: Total Hip Arthroplasty Methylprednisolone Phase IV: RCT, efficacy study NCT00968903 Management of Postoperative Drug: Bupivacaine; Pain After Total Hip Arthroplasty Drug: Placebo Phase II/III: RCT NCT01040273 Switching Drug Therapy for the Drug: Rivaroxaban Prevention of Blood Clot Formation From Enoxaparin to Rivaroxaban After Orthopedic Surgery for Either Total Hip or Total Knee Replacement Phase III: RCT, pharmacodynamics study NCT01094886 Ketamine Associated With Drug: KetamineMorphine PCA After Total Hip Morphine; Drug: Arthroplasty Morphine; Drug: RCT, efficacy study Postoperative PCA NCT00797264 of Ketamine and morphine A randomised controlled trial to Injection of local determine if local wound infiltration anaesthethic into reduces chronic pain after lower joint during joint limb arthroplasty replacement + RCT standard ISRCTN96095682 anaesthetic; standard anaesthetic alone Thromboembolism; Arthroplasty, Replacement, Hip Comp 3494 Adt Nov-04 Jan-11 Boehringer http://ClinicalTrials.gov/show/NCT00168818 Sen Ingelheim Pharmaceuticals LOS; Postoperative Pain; Postoperative Nausea and Vomiting; Sleeping Quality; Fatigue; Inflammatory Response Osteoarthritis of Hip Comp 48 Not yet Rec Adt Apr-10 Jan-11 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT00968903 Adt Dec-09 Dec-10 Chang Gung Sen Memorial Hospital http://ClinicalTrials.gov/show/NCT01040273 Arthritis; Comp Osteoarthritis, Knee; Osteoarthritis, Hip; Thromboembolism 56 Adt Feb-10 Dec-10 Ortho-McNeil http://ClinicalTrials.gov/show/NCT01094886 Sen Janssen Scientific Affairs, LLC Arthroplasty, Replacement, Hip Rec 100 Adt Nov-08 Nov-10 Assistance Sen Publique Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT00797264 Hip replacement; Knee replacement Comp 600 Adt Nov-09 Sep-10 Southmead Sen Hospital (UK) http://www.controlledtrials.com/ISRCTN96095682 179 Treatment of Postoperative Pain After Total Hip Arthroplasty Using Intravenous Lidocaine Infusion Phase I/II: RCT, efficacy study NCT01108562 Hemorrhage Risk Prescribed Arixtra Retrospective, cohort study NCT01064362 Drug: Lidocaine; Postoperative Pain Other: Normal Saline Management After Total Hip Arthroplasty Drug: Fondaparinux sodium; Drug: Low molecular weight heparin (LMWH) Effect of Local Infiltration Drug: Ropivacaine Analgesia in Total Hip Arthroplasty Phase IV: RCT, efficacy study NCT00968955 Clinical Trial for Fibrin Sealant in Knee Surgery RCT, efficacy study NCT00440921 A Study Evaluating Efficacy and Safety of YM150 Compared to Enoxaparin in Subjects Undergoing Hip Replacement Surgery Phase II/III: RCT, safety/efficacy study NCT00902928 Can Risedronate Prevent Periprosthetic Bone Loss After Total Hip Arthroplasty Phase IV: RCT, efficacy study NCT00772395 Randomised controlled trial to assess the difference of spinal anaesthesia versus general anaesthesia in hip replacement surgery RCT ISRCTN36381516 Drug: Single donor Allogenous Fibrin Sealant Knee Replacement Surgery; Haemorrhage; Thrombosis, Venous; Hip Replacement Surgery; Hip Fracture Surgery Post-operative Pain Total Kneereplacement; Total Hip-replacement Drug: YM150; Drug: Venous enoxaparin Thromboembolism; Arthroplasty, Replacement, Hip Drug: Risedronate; Drug: Placebo Bone Loss Spinal anaesthesia; Hip fracture; Hip General anaesthesia Replacement Adt Feb-08 Sep-10 Loma Linda http://ClinicalTrials.gov/show/NCT01108562 Sen University; Charles Lee MD; Michelle Schlunt MD Comp 1344 Adt Jan-10 Jun-10 GlaxoSmithKline http://ClinicalTrials.gov/show/NCT01064362 2 Sen Wdrwn 110 Comp 120 Adt Sep-09 Jun-10 Hvidovre http://ClinicalTrials.gov/show/NCT00968955 Sen University Hospital; Lundbeck Foundation Wdrwn 578 Adt Dec-08 Jun-10 Sanquin http://ClinicalTrials.gov/show/NCT00440921 Sen Research & Blood Bank Divisions; MDM Comp 1992 Adt Apr-09 Jun-10 Astellas Pharma http://ClinicalTrials.gov/show/NCT00902928 Sen Inc Active, NR 78 Adt Apr-06 May-10 Danderyd http://ClinicalTrials.gov/show/NCT00772395 Sen Hospital; SanofiAventis Comp 600 Adt Apr-07 Apr-10 Peterborough http://www.controlledSen and Stamford trials.com/ISRCTN36381516 Hospitals NHS Foundation Trust (UK) 180 A Study of DU-176b, Prevention of Venous Thromboembolism in Patients After Total Hip Arthroplasty Phase III: RCT, safety/efficacy study NCT01181167 Prevention of Venous Thromboembolism in Patients Undergoing Elective Total Hip Replacement Surgery Phase II/III: RCT, safety/efficacy study NCT00913120 Pharmacokinetic Study of the Penetration of Ceftobiprole in the Bone Phase I: RCT, pharmacokinetics study NCT00771524 Drug: edoxaban; Drug: enoxaparin sodium Comp 610 Adt May-09 Mar-10 Daiichi Sankyo http://ClinicalTrials.gov/show/NCT01181167 Sen Inc.; Daiichi Sankyo, Tokyo, LTD. Drug: YM150; Drug: Venous Placebo; Drug: Thromboembolism Enoxaparin Comp 610 Adt May-09 Mar-10 Astellas Pharma http://ClinicalTrials.gov/show/NCT00913120 Sen Inc Drug: Ceftobiprole Comp 22 Adt May-09 Feb-10 Ortho-McNeil http://ClinicalTrials.gov/show/NCT00771524 Sen Janssen Scientific Affairs, LLC Rec 400 Adt Apr-04 Jun-22 University http://ClinicalTrials.gov/show/NCT01118247 Sen Hospital of North Norway Rec 1000 Adt Nov-07 Oct-17 Massachusetts http://ClinicalTrials.gov/show/NCT00545285 Sen General Hospital; Biomet, Inc. Procedure Primary Uncemented Partly TiProcedure: coated Total Hip Prosthesis With Uncemented primary and Without HA, and Alumina-on- total hip arthroplasty alumina Articulation RCT, safety/efficacy study NCT01118247 Prevention; Venous Thromboembolism Hip Replacement, Total Survival of the Implants With Revision as Endpoint; Clinical Performance With HHS; Patients Satisfaction With the Hip Implant Long-Term Multi-center Evaluation Procedure: Total Hip Osteoarthritis of Hip; of E-Poly and Regenerex Arthroplasty Traumatic Arthritis of Non-randomized, parallel Hip assignment NCT00545285 Minimal Invasive Surgery in Total Procedure: Total hip Hip Osteoarthritis Hip Arthroplasty Patients; Short- replacement; and Long Term Results Procedure: Total hip Non-randomised, parallel replacement; assignment, efficacy study Procedure: Total hip NCT01506024 replacement Rec 60 181 Child Sep-11 Sep-16 Norwegian http://ClinicalTrials.gov/show/NCT01506024 Adt University of Sen Science and Technology; St. Olavs Hospital Study of Antibiotic Spacer Design to Treat Infection After Hip Replacement RCT, efficacy study NCT01373099 Procedure: Implantation of a static, nonarticulating cement spacer.; Procedure: Implantation of an articulating spacer. Hemi Artificial Hipjoint Versus Procedure: THA Total Artificial Hipjoint (Total hip Phase IV: RCT, safety/efficacy arthroplasty) versus study Hemi NCT01432691 (hemialloplastik) Minimal Invasive Anterior Procedure: TransApproach Versus Trans-gluteal gluteal approach, Approach for Hemi-arthroplasty in CLAS; Procedure: Femoral Neck Fractures Anterior minimal Phase IV: RCT, efficacy study invasive approach, NCT01408693 AMIS Cementless One-stage Revision of Procedure: the Chronic Infected Hip Cementless oneArthroplasty stage surgical Single group assignment, revision safety/efficacy study NCT01015365 Safety and Efficacy of the SL Procedure: primary PLUS and the SL PLUS MIA Hip total hip arthroplasty Stem Phase IV: RCT, safety/efficacy study NCT01435850 Anterolateral Versus Posterolateral Procedure: Approach to the Fractured Hip Anterolateral Arthroplasty approach Non-randomised, parallel assignment, efficacy study NCT01486641 Osteoarthritis; Hip Infection; Prosthetic Joint Infection; Complications; Arthroplasty, Infection or Inflammation; Complications; Arthroplasty Optimized Treatment Rec 80 Adt Aug-11 Aug-16 Rush University http://ClinicalTrials.gov/show/NCT01373099 Sen Medical Center; Thomas Jefferson University; Central DuPage Hospital Rec 70 Sen Jun-10 Jun-15 Hvidovre University Hospital Femoral Neck Fracture Rec 190 Adt Aug-11 Dec-14 University http://ClinicalTrials.gov/show/NCT01408693 Sen Hospital, Basel, Switzerland Infection; Hip Replacement Arthroplasty Rec 100 Adt Nov-09 Apr-14 University of Sen Aarhus Joint Replacement; Hip Rec 90 Adt Apr-09 Apr-14 Smith & Nephew http://ClinicalTrials.gov/show/NCT01435850 Sen Orthopaedics AG Femoral Neck Fracture Rec 160 Adt Feb-12 Jan-14 Sundsvall Sen Hospital 182 http://ClinicalTrials.gov/show/NCT01432691 http://ClinicalTrials.gov/show/NCT01015365 http://ClinicalTrials.gov/show/NCT01486641 Importance of Restoring Biomechanical Correct Hip Anatomy During Total Hip Arthroplasty RCT, efficacy study NCT01512550 Periprosthetic Bone Remodeling Around a Short and a Conventional Femoral Stem in Total Hip Arthroplasty RCT, efficacy study NCT01319227 Evaluation of Four Surgical Techniques in Primary Total Hip Arthroplasty RCT, efficacy study NCT01031732 Procedure: GF hip Osteoarthritis guide; Procedure: Stryker Navigation System; Device: ABG II modular femoral component; Device: ABG II femoral component Procedure: Hip Hip Arthroplasty replacement Procedure: MIS-2 THA; Procedure: MIS-WJ; Procedure: MIS-AL THA; Procedure: MIS-PL THA Follow up Study of Patients Procedure: Total Hip Undergoing Total Hip Arthroplasty Arthroplasty CERAFIT® Grafted With Poly Replacement Sodium Styrene Sulfonate Phase I/II: Single group assignment, safety study NCT01454271 Prospective Randomized Procedure: Total hip Comparison of Bipolar arthroplasty; Hemiarthroplasty and Total Hip Procedure: Arthroplasty With Large Femoral Hemiarthroplasty Heads for the Treatment of Displaced Intracapsular Femoral Neck Fractures in the Elderly Phase I: RCT, safety/efficacy study NCT01109862 A Comparison of Two Different Procedure: Surgical Surgical Techniques in Hip approach (ReCap Resurfacing Arthroplasty Hip Resurfacing RCT, efficacy study System) NCT00913679 Arthroplasty, Replacement, Hip Hip Arthroplasty Replacement Active, NR 75 Adt Jan-10 Dec-13 Region Skane Sen http://ClinicalTrials.gov/show/NCT01512550 Rec 50 Adt Oct-09 Dec-13 Danderyd Sen Hospital; Johnson & Johnson http://ClinicalTrials.gov/show/NCT01319227 Rec 120 Child Nov-09 Dec-13 Chang Gung Adt Memorial Sen Hospital; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01031732 Not yet Rec 50 Adt Dec-11 Dec-13 Laboratoire http://ClinicalTrials.gov/show/NCT01454271 Sen Ceraver-Osteal Femoral Neck Fractures Rec 80 Sen Apr-10 Dec-13 Wolfson Medical http://ClinicalTrials.gov/show/NCT01109862 Center Osteonecrosis; Femoral Neck Fracture; Implant Failure Rec 50 Adt Nov-08 Nov-13 University of http://ClinicalTrials.gov/show/NCT00913679 Aarhus; Aarhus University Hospital; Biomet, Inc. 183 A Trial Comparing Mini-posterior Approach and Direct Anterior Approach RCT, efficacy study NCT01024309 Procedure: MiniOsteoarthritis Posterior surgical approach for total hip arthroplasty; Procedure: Direct Anterior surgical approach for total hip arthroplasty Procedure: Hip Hip Osteoarthritis arthroplasty Rec 112 Obesity's Impact on the Effect of Rec 100 Hip Arthroplasty Prospective, cohort study NCT01496716 Benefit of Orthopedic Navigation in Procedure: Manual Osteoarthritis, Hip; Rec 80 the ARThroplasty of the Hip Intervention; Arthritis, Phase IV: RCT Procedure: Rheumatoid; Femur NCT01496300 Navigated Head Necrosis Intervention Study Comparing a Nerve Block Procedure: Analgesia Not yet 106 With Spinal Opiate to Provide Pain ultrasound guided Rec Relief for Hip Replacement fascia iliaca block; Surgery Procedure: spinal RCT, safety/efficacy study morphine NCT01217294 Compaction Total Hip Arthroplasty Procedure: Bone Coxarthrosis Active, 20 (THA) Bilateral preparation NR Single group assignment, technique: efficacy study compaction; NCT00317889 Procedure: Bone preparation technique: broaching A Randomised Trial Comparing Procedure: Minimally Osteoarthritis; Rec 50 Anterior Versus Posterior Invasive Anterior Rheumatoid Arthritis Approach in Total Hip Approach; Replacement Procedure: Standard RCT, efficacy study postero-lateral NCT01106560 approach Gait Analysis of Anterior Versus Procedure: Anterior Osteoarthritis Rec 64 Posterior Approach in Approach; Performance of Total Hip Procedure: Posterior Arthroplasty Approach Non-randomized, parallel assignment NCT00951951 184 Adt Nov-09 Jun-13 OrthoCarolina Sen Research Institute, Inc. http://ClinicalTrials.gov/show/NCT01024309 Adt Nov-11 Apr-13 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT01496716 Adt Nov-11 Apr-13 Aesculap AG Sen http://ClinicalTrials.gov/show/NCT01496300 Adt Apr-11 Apr-13 University of http://ClinicalTrials.gov/show/NCT01217294 Sen Glasgow; NHS Greater Glasgow and Clyde Adt Jan-04 Jan-13 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00317889 Adt Jan-10 Jan-13 Medacta http://ClinicalTrials.gov/show/NCT01106560 Sen International SA Adt Jun-09 Dec-12 Medacta USA; http://ClinicalTrials.gov/show/NCT00951951 Sen Medacta International SA Compaction Total Hip Arthroplasty (THA) Unilateral RCT, efficacy study NCT00318396 Procedure: Bone Coxarthrosis preparation technique: compaction; Procedure: Bone preparation technique: broaching Comparison of Hip Resurfacing to Procedure: Hip Osteoarthritis; Large Femoral Head Total Hip replacement Avascular Necrosis Arthroplasty Single group assignment, efficacy study NCT00175487 Comparison of Two Minimally Procedure: hip Osteoarthritis Invasive Surgical Techniques for surgery Hip Replacement Phase I: Single group assignment, efficacy study NCT00175461 A Telemedicine Solution for Procedure: remote Quality of Life; Remote Support of Rehabilitation, rehabilitation support Anxiety for Patients Undergoing, Total Hip Arthroplasty Surgery RCT, safety/efficacy study NCT00969020 Evaluation of the Wear of Vitamin Procedure: Hip Osteoarthritis of Hip; E Treated Polyethylene replacement Traumatic Arthritis of Components in Primary THA Using Hip RSA Single group assignment NCT00551967 A Randomized Controlled Trial of Procedure: Waiting Osteoarthritis Long Versus Short Wait For time (access time to Primary Total Hip and Knee Total joint Arthroplasty replacement) Phase IV: Single group assignment, efficacy study NCT00138892 Active, NR 40 Adt Sen Active, NR 108 Adt Sep-07 Dec-12 University of http://ClinicalTrials.gov/show/NCT00175487 British Columbia Active, NR 156 Adt Sep-05 Dec-12 University of http://ClinicalTrials.gov/show/NCT00175461 Sen British Columbia Rec 74 Rec 50 Child Sep-09 Nov-12 Regionshospital http://ClinicalTrials.gov/show/NCT00969020 Adt et Silkeborg; Sen Caretech Innovation; Lundbeck Foundation Adt Oct-07 Oct-12 Massachusetts http://ClinicalTrials.gov/show/NCT00551967 Sen General Hospital; Biomet, Inc. Active, NR 236 185 Dec-12 Northern Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00318396 Adt Aug-02 Oct-12 University of http://ClinicalTrials.gov/show/NCT00138892 Sen British Columbia Periprosthetic Bone Mineral Density After Total Hip Arthroplasty Performed Through a Minimally Invasive Anterior Approach (AMIS) With Either an AMIStem or a Quadra Femoral Component RCT, efficacy study NCT01285843 RSA for a Comparison of MIS vs. Standard Exposure in Total Hip Arthroplasty RCT NCT00405483 Mobility Assessment of Patients With Total Hip Arthroplasty Non-randomized, parallel assignment NCT00664508 Procedure: Anterior Osteoarthritis; Active, Minimally Invasive Arthritis; Avascular NR Approach (AMIS) Necrosis; Fracture of the Femoral Neck or Head; Congenital Hip Dysplasia 40 Procedure: Min Osteoarthritis Invasive vs standard exposure in hip arthroplasty; Procedure: Minimally Invasive Procedure: Motion Osteoarthritis; analysis; Procedure: Arthroplasty; Hip Motion analysis; Replacement Procedure: Motion analysis Active, NR 100 Rec 30 Efficacy of Preoperative Education Procedure: Osteoarthritis of the and Mini-invasive Surgery for Total preoperative Hip Hip Replacement education and total Phase III: RCT, efficacy study hip replacement NCT00449228 Effect of Prophylactic Antibiotics Procedure: Infection; Arthroplasty; Hip; on Intra-Operative Culture Results Prophylactic Knee Phase IV: RCT, efficacy study Antibiotics; NCT01174212 Procedure: Control Antibiotics The Influence of Anesthetic Procedure: spinal Primary Total Hip Technique on Post-operative Pain anesthesia vs lumbar Arthroplasty Scores and Range of Motion in plexus block with Primary Total Hip Arthroplasty general anesthesia RCT, safety/efficacy study NCT01359865 Child Sep-10 Sep-12 Medacta http://ClinicalTrials.gov/show/NCT01285843 Adt International SA Sen Adt Oct-05 Aug-12 Dalhousie University; Wright Medical Technology Adt Nov-07 Jul-12 Ottawa Hospital Sen Research Institute; Canadian Institutes of Health Research Rec 215 Adt Apr-07 Jul-12 Assistance Sen Publique Hôpitaux de Paris; Cochin Hospital Rec 200 Adt Jul-10 Jul-12 Rush University Sen Medical Center; Rothman Institute Orthopaedics Not yet 70 Child Jul-11 Jul-12 Milton S. Rec Adt Hershey Medical Sen Center 186 http://ClinicalTrials.gov/show/NCT00405483 http://ClinicalTrials.gov/show/NCT00664508 http://ClinicalTrials.gov/show/NCT00449228 http://ClinicalTrials.gov/show/NCT01174212 http://ClinicalTrials.gov/show/NCT01359865 Rec 80 Adt Apr-09 Apr-12 Assistance Sen Publique Hopitaux De Marseille http://ClinicalTrials.gov/show/NCT00894218 Rec 100 http://ClinicalTrials.gov/show/NCT01443975 Procedure: Total hip Primary Arthrosis; arthroplasty Osteoarthritis Active, NR 50 Procedure: Bipolar hemiarthroplasty; Procedure: Internal fixation Femoral Neck Fractures Active, NR 222 Hip Arthroplasty Active, NR 50 Adt Sep-11 Mar-12 Northern Sen Orthopaedic Division, Denmark; Medichanical Engineering Adt 39783 Feb-12 Lovisenberg Diakonale Hospital; Helse Sor-Ost; Biomet, Inc.; Ullevaal University Hospital Adt Oct-02 Dec-11 Ullevaal Sen University Hospital; Norwegian Foundation for Health and Rehabilitation; The Research Council of Norway Adt Oct-01 Dec-11 Ottawa Hospital Sen Research Institute; Stryker Nordic New Tool of Subjective and Objective Functional Evaluation and the Quality of Life After Arthroplastic Surgery of the Hip and the Knee Assisted or Not by Computer and Mini-invasive Arthroplasty RCT NCT00894218 Clinical Evaluation on the Use of the X-pander Device Prospective, cohort study NCT01443975 Procedure: Arthroplasty Wear Measurements of E-Poly in an Uncemented THA With Either 32 or 36 mm Caput of Ceramics. RCT, safety/efficacy study NCT00804388 Hemiarthroplasty or Internal Fixation for Displaced Femoral Neck Fractures - 5 Years Follow up RCT, efficacy study NCT00764153 Hip Arthritis; Knee Arthritis Procedure: x-pander Osteoarthrosis; Total Hip Arthroplasty A Comparison of Two Type of Procedure: BMD; Stems in Revision Hip Arthroplasty Procedure: BMD Phase IV: RCT, safety/efficacy study NCT00253838 187 http://ClinicalTrials.gov/show/NCT00804388 http://ClinicalTrials.gov/show/NCT00764153 http://ClinicalTrials.gov/show/NCT00253838 Metal Ion Release From an FDA- Procedure: Total Hip Non-inflammatory Approved Metal-on-Metal Total Hip Replacement Degenerative Joint Replacement Implant Disease RCT NCT00962351 Active, NR 120 Evaluation of Functional Procedure: THA Osteoarthritis, Hip Comp 104 Rehabilitation in Patients Physiotherapy; Undergoing Physiotherapy After Procedure: No Total Hip Arthroplasty physiotherapy after RCT, efficacy study THA NCT01491048 A Randomised Multi-centre Study Procedure: DePuy Osteoarthritis(Primar Term 61 to Compare the Short-term MI System; y) Outcomes of Minimally Invasive Procedure: and Conventional Surgery in Conventional Primary Total Hip Replacement surgical technique Phase IV: RCT, safety/efficacy study NCT00208416 Acupuncture for Pain Management Procedure: Pain; Postoperative Wdrwn 90 After Hip or Knee Arthroplasty Acupuncture; Complications RCT, efficacy study Procedure: Sham NCT00455182 Acupuncture; Procedure: Standard medical care Total Hip Arthroplasty Compared Procedure: Internal Femoral Neck Active, 100 to Internal Fixation for Displaced fixation; Procedure: Fracture NR Intracapsular Fractures of the Total hip arthroplasty Femoral Neck RCT, efficacy study NCT01344772 A Clinical Evaluation of Metal Ion Procedure: metal on Osteoarthritis; Term 86 Release From Metal-on-Metal metal hip Avascular Necrosis; Cementless Total Hip Arthroplasty arthroplasty Traumatic Arthritis; Single group assignment, safety Rheumatoid Arthritis study NCT00757354 188 Adt Oct-03 Dec-11 Anderson http://ClinicalTrials.gov/show/NCT00962351 Sen Orthopaedic Research Institute; University of Western Ontario, Canada; DePuy Orthopaedics Adt Jul-09 Oct-11 Hospital de http://ClinicalTrials.gov/show/NCT01491048 Sen Clinicas de Porto Alegre Adt Oct-05 Sep-11 DePuy Sen International http://ClinicalTrials.gov/show/NCT00208416 Adt Mar-07 Jun-11 HealthEast Care http://ClinicalTrials.gov/show/NCT00455182 Sen System (US) Adt Feb-90 Jun-11 Danderyd Sen Hospital http://ClinicalTrials.gov/show/NCT01344772 Adt Mar-06 Jun-11 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT00757354 Sen Biomet U.K. Ltd. Local Anesthetic Infiltration and Infusion for Pain Control After Hip Replacement RCT, efficacy study NCT01409278 Minimally Invasive Surgery of the Hip Versus Standard Approach RCT NCT00261040 Effect of Cemented Stem Design on Periprosthetic Bone Mass Following Primary Total Hip Arthroplasty Prospective, case-only study NCT00293605 Pelvic Alignment Level (PAL™) Instrument Evaluation RCT NCT01312428 Procedure: Osteoarthritis Ropivacaine infiltration and saline infusion.; Procedure: Ropivacaine infiltration and infusion.; Procedure: Normal Saline Procedure: minimally Hip Arthroplasty; invasive total hip Osteoarthritis arthroplasty; Procedure: Standard Procedure: Total Hip Osteoarthritis Replacement Comp 105 Adt Aug-09 Jun-11 Saint Francis Sen Care Comp 40 Comp 120 Adt Jun-03 May-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00261040 Sen Research Institute; Zimmer, Inc. Adt Jan-04 Apr-11 Sheffield http://ClinicalTrials.gov/show/NCT00293605 Sen Teaching Hospitals NHS Foundation Trust Procedure: Pelvic Arthroplasty, Alignment Level Replacement, Hip (PAL) Instrument; Procedure: Total Hip Replacement Procedure: Mini Osteoarthritis Incision Approach; Procedure: 2 Incision Approach Term 60 Adt Feb-11 Mar-11 Stryker Sen Orthopaedics Active, NR 90 Adt Jun-06 Dec-10 Rush University http://ClinicalTrials.gov/show/NCT00594893 Sen Medical Center; Zimmer, Inc. Femoral Neck Fractures Active, NR 230 Sen Sep-04 Dec-10 Ullevaal University Hospital; Asker & Baerum Hospital http://ClinicalTrials.gov/show/NCT00491673 Femoral Neck Fractures Wdrwn 100 Sen Oct-04 Dec-10 Northern Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00317837 Study Comparing Mini-Incision Versus 2-Incision Approach for Total Hip Replacement RCT, efficacy study NCT00594893 A Prospective Randomized Trial of Procedure: Uncemented Versus Cemented Uncemented primary Hemiarthroplasty for Displaced bipolar Femoral Neck Fractures hemiarthroplasty of RCT, efficacy study the hip; Procedure: NCT00491673 Cemented primary bipolar hemiarthroplasty of the hip Bipolar Versus Unipolar Procedure: Unipolar Hemiarthroplasty for Patients With Hemiarthroplasty of a Hip Fracture the hip joint; RCT, efficacy study Procedure: bipolar NCT00317837 hemiarthroplasty 189 http://ClinicalTrials.gov/show/NCT01409278 http://ClinicalTrials.gov/show/NCT01312428 Study on Cemented Versus Noncemented Hemiarthroplasty in Elderly With Hip Fractures RCT, safety/efficacy study NCT00800124 Procedure: Hip Fracture cemented Landos prosthesis vs. uncemented Landos prosthesis Active, NR 300 Prospective randomised study comparing the Furlong uncemented total hip replacement with the Birmingham resurfacing prosthesis RCT, efficacy study ISRCTN00324631 Can the Femoral Nerve Block be Improved by Ultrasound Guidance? Phase IV: RCT, efficacy study NCT00696150 Furlong uncemented Hip replacement total hip replacement; Birmingham resurfacing prosthesis Comp 100 Procedure: determination of method with highest efficacy (ultrasound or nerve stimulator); Procedure: nerve stimulator; Procedure: loss of resistance Femoral Versus Psoas Continuous Procedure: Femoral Peripheral Nerve Blocks Following Nerve Block vs. Hip Arthroplasty Psoas Compartment Phase IV: RCT, efficacy study Nerve Block NCT00967980 The Warwick Arthroplasty Trial Total Hip RCT, efficacy study Arthroplasty; Hip ISRCTN33354155 Resurfacing Arthroplasty Pain; hip arthroplasty Not yet 269 Rec Sen Jun-05 Oct-10 Sykehuset Innlandet HF; Rikshospitalet University Hospital; Sykehuset Buskerud HF N/K Sep-00 Sep-10 Department of Health (UK) Adt Sen http://ClinicalTrials.gov/show/NCT00800124 http://www.controlledtrials.com/ISRCTN00324631 Jul-08 Aug-10 NHS Greater http://ClinicalTrials.gov/show/NCT00696150 Glasgow and Clyde; Golden Jubilee National Hospital Hip Arthroplasty; Hip Comp Pain 50 Adt Sep-09 Aug-10 University of Sen California, San Diego Osteoarthritis of the hip joint Comp 172 Rec 100 Adt Jun-07 May-10 University http://www.controlledSen Hospitals trials.com/ISRCTN33354155 Coventry and Warwickshire NHS Trust (UK) Adt Jun-07 Apr-10 Tennessee http://ClinicalTrials.gov/show/NCT00738803 Sen Orthopedic Alliance Comp 80 Restoration of Leg Length, Offset, Procedure: Total hip Arthritis and Center of Rotation in Total Hip replacement Replacement Single group assignment NCT00738803 Preheating of Femur Component Procedure: Total hip Osteoarthritis, Hip in Hybrid Total Hip Arthroplasty replacement Phase II: RCT, efficacy study (Preheating of femur NCT00319085 stem) 190 Sen May-06 Apr-10 Northern Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00967980 http://ClinicalTrials.gov/show/NCT00319085 Computer-assisted Minimally Invasive total hip Surgery (MIS): a randomised controlled trial into the effectiveness compared to traditional total hip arthroplasty RCT ISRCTN52538512 Other Genetics Informatics Trial (GIFT) of Warfarin to Prevent DVT Phase III: RCT, safety/efficacy study NCT01006733 Computer-assisted minimally invasive total hip surgery; total hip arthroplasty Total hip replacement due to primary or secondary osteoarthritis Other: Thromboembolism; Arthroplasty, Knee; Pharmacogenetic Arthroplasty, Hip Warfarin Initiation; Other: Clinical Warfarin Initiation (nonpharmacogenetic); Other: Pharmacogenetic Warfarin Initiation; Other: Clinical Warfarin Initiation (nonpharmacogenetic) Epsilon Aminocaproic Acid (EACA) Other: EACA; Other: Degenerative Joint for the Reduction of Blood Loss in Placebo arm Disease; Total Hip Arthroplasty (THA) Osteoarthritis RCT, safety study NCT01391182 Cell Saver Use in Bilateral Total Other: Cell Saver One-stage Bilateral Hip Arthroplasty (THA) Total Hip NCT01468129 Replacement Total Hip Arthroplasty (THA): Early Other: Early loading; Primary Total Hip Load Versus Load Late Other: Late loading Arthroplasty Non-randomized, parallel assignment, efficacy study NCT01495546 Liberal Versus Restrictive Other: Red blood cell Arthroplasty, Hip Transfusion During Symptomatic transfusion; Drug: Moderate Anemia After Hip Voluven Arthroplasty RCT, efficacy study NCT01452581 Comp Rec Rec 132 Adt Jan-07 Jan-10 University http://www.controlledSen Medical Center trials.com/ISRCTN52538512 Groningen (The Netherlands) 1600 Adt Mar-11 Aug-15 Washington http://ClinicalTrials.gov/show/NCT01006733 Sen University School of Medicine; Intermountain Health Care, Inc.; University of Utah; Hospital for Special Surgery, New York; National Heart, Lung, and Blood Institute (NHLBI) 120 Adt Jul-11 Jul-13 Mayo Clinic http://ClinicalTrials.gov/show/NCT01391182 Sen Rec N/K Rec 40 Rec 70 191 Adt Nov-11 Dec-12 Rothman http://ClinicalTrials.gov/show/NCT01468129 Sen Institute Orthopaedics Adt Dec-11 Dec-12 University of Sao http://ClinicalTrials.gov/show/NCT01495546 Paulo Adt Oct-11 Dec-12 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01452581 POMX (Post Operative Morbidity): Randomized controlled trial of chewing gum to reduce postoperative morbidity in elective orthopaedic surgery RCT, efficacy study ISRCTN20301599 Group Exercise After Hip Replacement Surgery RCT, efficacy study NCT01253798 Preoperative Resistance Training in Patients Scheduled for Total Hip Arthroplasty RCT NCT01164111 Optimising patient function following elective Total Hip Replacement (THR) surgery RCT ISRCTN13019951 Rehabilitation After Total Hip Arthroplasty - the Effect of Taskoriented Exercises RCT, efficacy study NCT00808483 Prospective Study Deltamotion DAA THA Study Prospective, cohort study NCT01474031 Preoperative Exercise in Patients Undergoing Total Hip or Knee Replacement RCT NCT01003756 Chewing gum Elective orthopaedic hip and knee arthroplasty procedures Active 106 Adt Sep-11 Sep-12 University http://www.controlledSen College London trials.com/ISRCTN20301599 (UK) Other: Group training Hip Osteoarthritis; Exercise; Hydrotherapy Rec 54 http://ClinicalTrials.gov/show/NCT01253798 Other: Preoperative Osteoarthritis; Hip resistance training Arthroplasty Rec 80 Training exercises in Total hip the pre-assessment replacement clinic & postoperatively and given information sheets + home visit by physiotherapist; Routine in- & outpatient physiotherapy + standard information leaflets Other: Task-oriented Total Hip exercises Arthroplasty; Taskoriented Exercises Comp 50 Child Nov-10 Jul-12 Norwegian Adt University of Sen Science and Technology Adt Oct-10 Jun-12 University of Sen Southern Denmark; University of Copenhagen N/K Mar-10 Mar-12 Bangor University (UK) Active, NR 72 Adt Oct-08 Dec-11 University of Sen Oslo http://ClinicalTrials.gov/show/NCT00808483 Rec 40 Comp 165 Adt Oct-11 Aug-11 Universitaire http://ClinicalTrials.gov/show/NCT01474031 Sen Ziekenhuizen Leuven; DePuy International Adt Nov-09 Aug-11 University of http://ClinicalTrials.gov/show/NCT01003756 Sen Southern Denmark; Odense University Hospital Other: biomechanics Arthroplasty, Replacement, Hip; Biomechanics Other: Preoperative Osteoarthritis neuromuscular exercise 192 http://ClinicalTrials.gov/show/NCT01164111 http://www.controlledtrials.com/ISRCTN13019951 Time to Total Hip Replacement After Supervised Exercise and Patient Education RCT, efficacy study NCT01338532 Transfusion Requirements in Orthopedic Surgery (PHASE 2) Prospective, cohort study NCT00726349 Wound closure following hip arthroplasty RCT, efficacy study ISRCTN70685656 Cost-Effectiveness of Web-Based Follow Ups RCT, safety/efficacy study NCT01079572 Other: A 12 week Hip Osteoarthritis supervised exercise program and patient education; Other: Patient education Other: No Total Hip or Knee intervention Arthroplasty Active, NR 109 Adt Mar-05 May-11 Oslo University Sen Hospital http://ClinicalTrials.gov/show/NCT01338532 Comp 305 http://ClinicalTrials.gov/show/NCT00726349 Standard absorbent dressing; DERMABOND® tissue adhesive Other: in-person; Other: web-based Comp 219 Adt May-08 May-11 Centre Sen hospitalier de l'Université de Montréal Adt Apr-10 Apr-11 NHS Greater Sen Glasgow and Clyde (UK) Elective Total Hip Replacemen Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Effects of a Late Phase Exercise Other: home based Program Following Total Hip exercise and Arthroplasty education program Prospective, case control study NCT00896259 Total Hip Arthroplasty Prophylactic Anticoagulation for Other: prophylactic Preventing Deep Vein Thrombosis anticoagulation After Total Hip Arthroplasty Phase II/III: RCT, safety/efficacy study NCT01446887 Deep Vein Thrombosis Miscellaneous observational studies Restoration® Anatomic Dual Mobility (ADM) X3® Acetabular System Prospective, cohort study NCT01420237 Rejuvenate Modular Outcomes Study Prospective, cohort study NCT01257568 http://www.controlledtrials.com/ISRCTN70685656 Rec 1000 Child Feb-10 Mar-11 University of http://ClinicalTrials.gov/show/NCT01079572 Adt Western Ontario, Sen Canada; The Physicians' Services Incorporated Foundation Comp 60 Adt Mar-09 Feb-11 Capital District http://ClinicalTrials.gov/show/NCT00896259 Sen Health Authority, Canada; Canadian Orthopaedic Foundation Comp Adt Jan-07 Feb-11 JIANG Qing http://ClinicalTrials.gov/show/NCT01446887 Sen Arthroplasty, Replacement, Hip Rec 350 Adt Jun-11 Aug-24 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT01420237 Arthroplasty, Replacement, Hip Rec 240 Adt Nov-10 Nov-22 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT01257568 193 A Clinical Investigation of ArComXL® Polyethylene in Total Hip Replacement Prospective, cohort study NCT00698152 Hospital for Special Surgery Hip Arthroplasty Cohort Prospective, cohort study NCT00454506 Osteoarthritis; Active, Avascular Necrosis; NR Rheumatoid Arthritis LFIT™ Anatomic CoCr Femoral Heads With X3® Polyethylene Insert Study Prospective, cohort study NCT00510458 Short-Term Clinical Outcome of Total Hip Arthroplasty Using Larger Diameter of 4th Generation Ceramic Bearing Prospective, cohort study NCT01103882 Vitamin D and Functional Outcomes After Total Hip Arthroplasty (THA) Prospective, cohort study NCT01397383 Length of Stay and Complications in High-risk Patients Receiving Fast-track Total Hip (THA) or Knee- Alloplasty (TKA) Prospective, cohort study NCT01515670 Alberta Hip Improvement Project Phase IV: Prospective, cohort study NCT00293774 Determination of Metal Ion Serum Levels and Cytokines in Total Hip Replacement Prospective, case control study NCT01394744 Arthroplasty, Replacement, Hip OR Arthroplasty Hip Arthroplasty 149 Child Jan-06 Apr-18 Biomet Adt Orthopedics, Sen LLC http://ClinicalTrials.gov/show/NCT00698152 Rec 3000 Adt Apr-07 Apr-17 Hospital for http://ClinicalTrials.gov/show/NCT00454506 Sen Special Surgery, New York; Agency for Healthcare Research and Quality (AHRQ) Active, 95 Adt Apr-07 Dec-15 Stryker http://ClinicalTrials.gov/show/NCT00510458 NR Sen Orthopaedics Arthropathy of Hip Rec 277 Adt May-10 May-15 Biomet, Inc. Sen Vitamin D Deficiency Rec 200 Adt Mar-10 Mar-15 Hospital for http://ClinicalTrials.gov/show/NCT01397383 Sen Special Surgery, New York Arthroplasty Complications; Preoperative Comorbidity; Postoperative Morbidity Arthroplasty, Replacement, Hip Rec 3000 Adt Feb-10 Jan-15 Rigshospitalet, 0 Sen Denmark Rec 1000 Adt Total Hip Replacement Rec 30 194 http://ClinicalTrials.gov/show/NCT01103882 http://ClinicalTrials.gov/show/NCT01515670 Jun-04 Sep-14 Alberta Bone http://ClinicalTrials.gov/show/NCT00293774 and Joint Health Institute Adt Aug-11 Jan-14 University of Sen Munich (German) http://ClinicalTrials.gov/show/NCT01394744 Evaluation of Weight Bearing After Total Hip and Knee Replacement Prospective, cohort study NCT01135160 Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery Prospective, cohort study NCT00847301 Postoperative Anemia and Functional Outcomes After Fasttrack Primary Hip Arthroplasty Prospective, cohort study NCT01514006 Arthroplasty, Replacement, Hip; Total Knee Arthroplasty Arthroplasty, Replacement; Thromboembolism Not yet 200 Child Aug-12 Dec-13 Kantonsspital Rec Adt Münsterlingen Sen Arthroplasty, Hip Replacement; Anemia Not yet 125 Rec Metal Ions in Ceramic on Metal Total Hip Arthroplasty Prospective, cohort study NCT01437124 Osteoarthritis; Not yet Avascular Necrosis; Rec Rheumatoid Arthritis; Developmental Dysplasia of the Hip Coxarthrosis Active, NR 83 Knee Replacement; Hip Replacement; Hyperglycemia Active, NR 200 Rec 60 Migration Pattern of C-stem AMT Versus Exeter in Total Hip Arthroplasty Prospective, case control study NCT00722982 Perioperative Hyperglycaemia in Primary Total Hip and Knee Replacement Prospective, cohort study NCT01021826 Functional Recovery After Partial Hip Arthroplasty: Anterior or Posterolateral Approach? Prospective, case control study NCT01520961 Hip Arthroplasty; Femoral Neck Fractures Rec 500 70 195 http://ClinicalTrials.gov/show/NCT01135160 Adt Apr-09 Apr-13 Boehringer http://ClinicalTrials.gov/show/NCT00847301 Sen Ingelheim Pharmaceuticals Adt Jan-12 Feb-13 Rigshospitalet, Sen Denmark; University Hospital, Gentofte, Copenhagen; Vejle Hospital Adt Oct-11 Dec-12 Hussain Kazi Sen Adt Sen Jul-08 http://ClinicalTrials.gov/show/NCT01514006 http://ClinicalTrials.gov/show/NCT01437124 Jul-12 Ullevaal http://ClinicalTrials.gov/show/NCT00722982 University Hospital; Ringerike hospital HF, Hønefoss Norway; Ortomedic AS, Lysaker Norway; Helse Sor-Ost Adt Dec-09 Jul-12 Coxa, Hospital http://ClinicalTrials.gov/show/NCT01021826 Sen for Joint Replacement; University of Tampere Adt Dec-11 May-12 Hôpital http://ClinicalTrials.gov/show/NCT01520961 Sen Ambroise Paré Serum Metal Ion Concentrations Following Primary Hip Arthroplasty Cross-sectional, case-only study NCT00714610 Stem Cells Predicting Orthopedic Outcomes Prospective study NCT01366911 Preoperative Pain, Function, and Activity for Total Hip and Knee Arthroplasty Patients Prospective, cohort study NCT01248039 Thigh Swelling, Hip-muscle Strength, and Functional Performance Following Total Hip Arthroplasty Prospective, cohort study NCT01246674 Surgical Field Bacterial Contamination in Primary Total Hip (THA) and Knee (TKA) Arthroplasty Prospective, cohort study NCT01493375 Tissue Culture Versus Swab Culture in Prosthetic Joint Infections Prospective, cohort study NCT01482533 Cognition in Postoperative Total Hip Arthroplasty and Total Hip Resurfacing Patients Prospective, cohort study NCT01079468 Medium and Long Term Outcome of Total Hip Arthroplasty Using Accolade TMZF Femoral Stem Case-only study NCT00951145 Healthy Active, NR 110 Adt Jun-07 May-12 University of Sen Utah http://ClinicalTrials.gov/show/NCT00714610 Invite 50 Child Apr-11 Apr-12 University of Adt Nebraska Sen http://ClinicalTrials.gov/show/NCT01366911 Arthroplasty Rec 100 http://ClinicalTrials.gov/show/NCT01248039 Osteoarthrosis Patients With Total Hip Arthroplasty Rec 30 Adt Jan-11 Jan-12 Hvidovre Sen University Hospital; Lundbeck Foundation Adt Jan-11 Jan-12 Hvidovre Sen University Hospital; Lundbeck Foundation Comp 60 Adt Jun-10 Dec-11 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT01493375 Hip Arthroplasty Prosthetic Infections http://ClinicalTrials.gov/show/NCT01246674 Revision Total Hip Not yet N/K Arthroplasty; Rec Revision Total Knee Arthroplasty Adt Sen Nov-11 Rothman Institute Orthopaedics http://ClinicalTrials.gov/show/NCT01482533 Cognition Comp 100 Adt Jan-10 Nov-11 Rothman Sen Institute Orthopaedics http://ClinicalTrials.gov/show/NCT01079468 Osteoarthritis of the Hip Active, NR N/K Child Adt Sen Nov-11 Rothman Institute Orthopaedics; Stryker Orthopaedics http://ClinicalTrials.gov/show/NCT00951145 196 N/K N/K Postoperative Sleep Disturbances Role in Cognitive Test Results After Fast-track Hip and Knee Arthroplasty Prospective study NCT01383369 Pradaxa (Dabigatran Etexilate 220 mg/q.d. in the General Population After Hip or Knee Replacement Surgery Prospective, cohort study NCT00846807 Outcomes Following Anterior Approach to Total Hip Arthroplasty Prospective, cohort study NCT01353885 Impact of Spontaneous Breathing on Ventilation Distribution in Obese Patients Prospective, case control study NCT01382927 Dual Energy X-rayY Absorptiometry (DXA) Comparison Hip Resurfacing Versus Total Hip Arthroplasty (THA) Prospective, case control study NCT01359527 Femoral Remodeling Following Total Hip Arthroplasty With Omni Apex Modular™, OMNI Apex ARC™ Stem, and Omni Apex "Conical Stem" Compared to Competitive Designs Prospective, case control study NCT01359540 Effect of Rivaroxaban on Coagulation Parameters- an ex Vivo Study Retrospective, cohort study NCT00986635 Postoperative Cognitive Abilities Comp 20 Adt Feb-11 Aug-11 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01383369 Arthroplasty, Replacement; Thromboembolism Comp 5476 Adt Feb-09 Jul-11 Boehringer http://ClinicalTrials.gov/show/NCT00846807 Sen Ingelheim Pharmaceuticals Osteoarthritis, Hip Not yet 700 Rec Jul-11 Jul-11 McMaster University; DePuy Orthopaedics Adt Apr-11 Jun-11 Dresden Sen University of Technology http://ClinicalTrials.gov/show/NCT01353885 Adt Sen Obesity; Hip Arthroplasty; General Anesthesia; Spinal Anesthesia; Atelectasis Total Hip Replacement; Osteoarthritis; Bone Loss Rec 16 Rec 25 Child Dec-08 May-11 Spokane Joint Adt Replacement Sen Center http://ClinicalTrials.gov/show/NCT01359527 Osteoarthritis of the Hip Rec 75 Child Nov-09 May-11 Spokane Joint Adt Replacement Sen Center http://ClinicalTrials.gov/show/NCT01359540 100 Adt Sep-09 Apr-11 Johann Sen Wolfgang Goethe University Hospitals http://ClinicalTrials.gov/show/NCT00986635 Hip or knee Comp replacement surgery 197 http://ClinicalTrials.gov/show/NCT01382927 Effect of Dabigatran on Coagulation parameters-an ex Vivo Study Retrospective, cohort study NCT01112202 Recovery at the Post Anaesthetic Care Unit After Hip and Knee Arthroplasty Prospective, cohort study NCT01178489 Why in Hospital - Factors Determining Time to Discharge Readiness After Arthroplasty Surgery Prospective, case-only study NCT01047371 Cardiovascular Changes and Changes in Tissue Oxygenation During Early Postoperative Mobilization in Total Hip Arthroplasty (THA) Patients Prospective, cohort study NCT01089946 Physical Functioning Following Total Hip Arthroplasty Prospective, cohort study NCT00651430 Study to evaluate the safety and efficacy of pradaxar for the prevention of venous thromboembolism in the Mexican population undergoing elective total hip or knee replacement surgery Prospective, cohort study NCT00967447 Hip or knee Comp replacement surgery 70 PACU Stay After THA or TKA Under Spinal Anaesthesia Comp 170 Arthroplasty, Hip; Arthroplasty, Knee Comp Arthroplasty Adt Apr-10 Apr-11 Johann Sen Wolfgang Goethe University Hospitals Adt Aug-10 Jan-11 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01112202 200 Adt Jan-10 Aug-10 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT01047371 Comp 26 Adt Mar-10 Jun-10 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01089946 Osteoarthrosis, Comp Balance Control, Voluntary Movement Control Thromboembolism; Term Arthroplasty, Replacement, Hip 30 Adt Mar-08 May-10 Soroka Sen University Medical Center http://ClinicalTrials.gov/show/NCT00651430 N/K Adt Feb-09 Mar-10 Boehringer http://ClinicalTrials.gov/show/NCT00967447 Sen Ingelheim Pharmaceuticals 198 http://ClinicalTrials.gov/show/NCT01178489 A8D: OTHER Title Phases: trial design (control) CT ID Behavioural Supporting Decision Making for Musculoskeletal PreferenceSensitive Care RCT NCT01345123 EMPART - Exercise and Manual Physiotherapy Arthritis Research Trial Phase III: RCT NCT00709566 Hip Osteoarthritis: Effects of Exercise Programs on Pain and Disability RCT, efficacy study NCT00682617 Device 10 Year Clinical Evaluation of Primoris Hip Component Prospective, cohort study NCT01326832 Tritanium® Primary Acetabular Shell Study Single group assignment NCT01063751 Interventions Conditions Behavioral: Provision Knee Pain Chronic; of condition specific Arthritis (Hip); DVD and Pamphlet Arthritis (Knee); to support Shared Back Pain Decision Making; Behavioral: Telephonic outreach and support by Health Coach; Behavioral: No condition specific telephonic outreach Behavioral: Exercise Hip Osteoarthritis therapy; Behavioral: Combined exercise and manual therapy Recruit n Age Start (Grp) Date End Sponsors Date URL Active, 18000 Adt Feb-11 Mar-12 Health Dialog; http://ClinicalTrials.gov/show/NCT01345123 NR Sen Foundation for Informed Medical Decision Making; University of Massachusetts, Boston Active, NR 150 Adt Apr-08 Dec-10 Royal College of http://ClinicalTrials.gov/show/NCT00709566 Sen Surgeons, Ireland Behavioral: Hip Osteoarthritis Structured exercise program; Behavioral: Waitlist, delayed intervention Rec 30 Adt Aug-06 Jul-10 Oregon Health Sen and Science University Device: Primoris Rec 400 Adt Sep-11 Dec-24 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT01326832 Biomet Denmark A/S Rec 240 Adt Sen Coxarthrosis Device: Tritanium® Osteoarthritis; Primary Acetabular Traumatic Arthritis; Shell; Device: Avascular Necrosis Tritanium® Primary Acetabular Shell with Periapatite 199 Jul-11 Jul-24 Stryker Orthopaedics http://ClinicalTrials.gov/show/NCT00682617 http://ClinicalTrials.gov/show/NCT01063751 The Metaphyseal Hip Prosthesis Total Hip RCT, safety/efficacy study NCT01501955 A Clinical Investigation of the C2aTaper™ Acetabular System Single group assignment NCT00578851 Device: Metaphyseal Hip Prosthesis; Device: Stanmore hip prosthesis Device: C2a Taper™ Acetabular System Osteoarthritis of the Hip Not yet Rec 50 Adt Mar-12 Mar-23 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01501955 Osteoarthritis; Active, Avascular Necrosis; NR Congenital Hip Dysplasia; Traumatic Arthritis Trilogy AB Acetabular Hip System Device: Trilogy AB Osteoarthritis; Rec Post Approval Study Acetabular Ceramic Avascular Necrosis; Phase IV: Single group Hip System Congenital Hip assignment, safety/efficacy Dysplasia; Traumatic study Arthritis NCT00715026 ReCap Total Hip Resurfacing Device: ReCap Total Arthritis Rec Prospective Data Collection Hip Resurfacing Prospective, cohort study NCT00758472 A Safety and Efficacy Study of the Device: Birmingham Arthritis Rec Birmingham Hip Resurfacing Hip Resurfacing System System Single group assignment, safety/efficacy study NCT00611585 Post-PMA Approval Study: 10 Device: Cormet Hip Osteoarthritis; Invite Year Follow-Up IDE Subjects Resurfacing System Avascular Necrosis; Prospective, cohort study Rheumatoid Arthritis NCT00721994 A Prospective Clinical Study On A Device: ReCap Total Arthritis; Avascular Rec Total Hip Resurfacing System Hip Resurfacing Necrosis Single group assignment, System safety/efficacy study NCT00604734 A Prospective Clinical Study On A Device: ReCap Total Arthritis; Avascular Active, Total Hip Resurfacing System Hip Resurfacing Necrosis NR Single group assignment, System safety/efficacy study NCT00603395 34 Adt Apr-06 Apr-22 Biomet Sen Orthopedics, LLC http://ClinicalTrials.gov/show/NCT00578851 250 Adt Apr-09 Apr-21 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT00715026 500 Adt Mar-05 Mar-20 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT00758472 Sen Biomet U.K. Ltd. 400 Adt Sep-06 Sep-18 Smith & Sen Nephew, Inc. http://ClinicalTrials.gov/show/NCT00611585 450 Child May-08 May-18 Corin Adt Sen http://ClinicalTrials.gov/show/NCT00721994 500 Child Oct-04 Oct-17 Biomet, Inc. Adt Sen http://ClinicalTrials.gov/show/NCT00604734 300 Child Sep-04 Sep-17 Biomet, Inc.; Adt Knowledge Sen Center for Orthopedic Surgery, St. Anna Hospital, Geldrop, Netherlands http://ClinicalTrials.gov/show/NCT00603395 200 Cementless Alumina-Alumina Device: Total Hip and Hybrid Alumina/Alumina; Phase III: RCT, safety/efficacy Device: Standard study NCT00764530 Evaluation of the Trabecular Device: Zimmer Metal™ Revision Hip Cup Using Trabecular Metal Bone Mineral Density (DEXA) Revision Cup; Phase IV: RCT, efficacy study Device: Zimmer NCT01183260 Modular Cup A Migration and Bone Density Device: Hi-Fatigue Study Comparing Hi-Fatigue Bone Bone Cement; Cement and Palacos Bone Device: Palacos Cement Bone Cement Phase II: RCT, safety/efficacy study NCT01289834 Local Gentamicin Application to Device: CollagenReduce Postoperative Infection gentamicin sponge Rate Phase III: RCT, efficacy study NCT01287780 Post PMA-Approval Study: New Device: Cormet Hip Enrollment Post PMA-Approval Resurfacing Study Post-approval Study Group (New Enrollment) Phase IV: Single group assignment, safety/efficacy study NCT00722007 Study of Low-Magnitude, HighDevice: LowFrequency Vibration Treatment on magnitude high Osteoporotic Hip Fracture Healing frequency vibration Phase II/III: RCT, safety/efficacy treatment study NCT01293721 Comparison of Conventional and Device: Large Large Diameter Femoral Heads for Diameter Femoral the Prevention of Hip Dislocation Head RCT, efficacy study NCT00175500 Rheumatoid Arthritis; Active, Osteoarthritis; PostNR traumatic Arthritis; Avascular Necrosis 342 Adt Nov-03 Nov-14 Encore Medical, http://ClinicalTrials.gov/show/NCT00764530 Sen L.P. Revision, Joint Rec 20 Adt Aug-10 Aug-14 The Cleveland Sen Clinic; Zimmer, Inc. Hip Arthritis Rec 50 Sen Aug-10 Aug-13 University of http://ClinicalTrials.gov/show/NCT01289834 Aarhus; Aarhus University Hospital; Zimmer, Inc. Surgical Wound Infection Rec 800 Child Jan-11 Dec-12 Oslo University Adt Hospital Sen http://ClinicalTrials.gov/show/NCT01287780 Osteoarthritis; Avascular Necrosis; Rheumatoid Arthritis Rec 160 Child Apr-08 Dec-12 Corin Adt Sen http://ClinicalTrials.gov/show/NCT00722007 Hip Fracture Rec 40 Adt May-07 Dec-12 Chinese Sen University of Hong Kong Fonly http://ClinicalTrials.gov/show/NCT01293721 Active, NR 400 Adt Sep-07 Dec-12 University of http://ClinicalTrials.gov/show/NCT00175500 Sen British Columbia Hip Dislocation 201 http://ClinicalTrials.gov/show/NCT01183260 Balloon Assisted Hip Arthroscopy Clinical Evaluation of a New Tool for Hip Arthroscopy Single group assignment, safety/efficacy study NCT01429805 Multi-Center Comparative Trial of the ASR™-XL Acetabular Cup System vs. the Pinnacle™ Metalon- Metal Total Hip System Phase IV: RCT, safety/efficacy study NCT00561600 A Randomised Study to Compare Metal Ion Release and Long-term Performance of the Pinnacle™ Cup With a Ceramic-on-Metal or a Metal-on-Metal Bearing Phase IV: RCT, safety/efficacy study NCT00873444 Study Performance of The Plexur P™ Bone Void Filler Device in Patients Undergoing Iliac Crest Harvesting Procedures Single group assignment, safety/efficacy study NCT00837473 Clinical Study on BiHapro Total Hip System With Different Surface Coatings Prospective, cohort study NCT00755001 Bone Remodeling Around HAcoated Acetabular Cups. Phase IV: RCT, efficacy study NCT00159497 Device: HipJack Balloon Spacer Hip Arthroscopy Rec 40 Adt Sep-11 Feb-12 Pivot Medical Sen Inc. http://ClinicalTrials.gov/show/NCT01429805 Device: ASR™-XL Osteoporosis; Modular Acetabular Arthritis; Trauma Cup System; Device: Pinnacle™ acetabular shell Comp 300 Adt Aug-06 Jan-12 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00561600 Device: Pinnacle™ Acetabular System; Device: Pinnacle™ Acetabular System Term 190 Adt Sen Active, NR 15 Adt Jan-09 Oct-11 Osteotech, Inc Sen http://ClinicalTrials.gov/show/NCT00837473 Term 40 Child May-07 May-11 Biomet, Inc.; Adt Biomet Spain Sen Orthopaedics S.L. http://ClinicalTrials.gov/show/NCT00755001 Comp 100 Adt Oct-98 Jan-11 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT00159497 Osteoarthritis; Posttraumatic Arthritis; Collagen Disorders; Avascular Necrosis; Congenital Hip Dysplasia; Slipped Capital Femoral Epiphysis Device: Plexur-P Iliac Crest used as a Bone Void Harvesting Filler in Iliac Crest Procedure-Bone Harvesting Void Filler; Procedures Device: BiHapro hip Osteoarthritis stem with PPS Ti+Plasma HA; Device: BiHapro hip stem with PPS Ti+BoneMaster HA Device: porous Coxarthrosis coated Trilogy®; Device: Trilogy Calcicoat® 202 Jul-06 Jan-12 DePuy International http://ClinicalTrials.gov/show/NCT00873444 Metal on Metal Versus Metal on Highly Crossed Linked Polyethylene Sytem Phase IV: RCT, safety/efficacy study NCT01422564 Device: Metal on Metal Hip System; Device: Highly Cross Linked Polyethylene cup System Osteoarthritis; Term Avascular Necrosis; Rheumatoid Arthritis; Congenital Dysplasia of the Hip; Ankylosing Spondylitis; Posttraumatic; Arthrosis; Injury of Hip and Thigh Aortic Diseases; Active, Osteoarthritis, Hip NR 41 Adt Jan-07 Dec-10 Capital District http://ClinicalTrials.gov/show/NCT01422564 Sen Health Authority, Canada; University Health Network, Toronto 20 Adt Nov-09 May-10 Sykehuset i Sen Vestfold HF; Oslo University Hospital; Astra Tech AB http://ClinicalTrials.gov/show/NCT00851149 Comp 150 Adt Feb-09 Jan-10 Hopital de Sen l'Enfant-Jesus http://ClinicalTrials.gov/show/NCT01469871 Rec 24 Child Aug-09 Aug-15 University of Adt Aarhus http://ClinicalTrials.gov/show/NCT00964639 Invite 342 Adt Jan-12 Jan-15 University of Sen Utah http://ClinicalTrials.gov/show/NCT01539447 Drug: Placebo; Drug: Degenerative Joint Gapabentin Disease of Hip and Knee. Rec 90 Drug: Zoledronic Osteonecrosis Acid; Drug: Placebo Rec 120 Adt Mar-12 Dec-14 University of http://ClinicalTrials.gov/show/NCT01546857 Sen Medicine and Dentistry New Jersey Adt Aug-09 Dec-13 University of http://ClinicalTrials.gov/show/NCT00781261 Sen Sydney; Novartis Pro-inflammatory Cytokines in Device: Sangvia Blood From Orthopedic Surgery blood sampling Compared to Abdominal Aneurysm system Repair Prospective, case control study NCT00851149 Evaluation of Three Types of Device: Dressing of Tape Blisters; Hip Dressings After Hip Surgery wound; Device: Surgery Phase IV: RCT, efficacy study Dressing of wound; NCT01469871 Device: Dressing of wound Drugs including biologics Postoperative Pain in Children With Cerebral Palsy After Pelvic and Femoral Osteotomies Phase IV: RCT NCT00964639 Influence of Naproxen on Heterotropic Bone Formation Following Hip Arthroscopy RCT, efficacy study NCT01539447 Effect of Gabapentin on Orthopedic Pain Phase IV: RCT, efficacy study NCT01546857 Osteonecrosis of the Hip and Bisphosphonate Treatment Phase II: RCT, efficacy study NCT00781261 Drug: Ropivacaine; Drug: Saline Postoperative Pain; Cerebral Palsy Drug: Naproxen; Drug: placebo Hip Arthroscopy 203 Autologous Chondrocyte Intraarticular Implantation in Patients With Severe Hip Osteoarthritis Phase I: Single group assignment, safety study NCT01500811 Efficacy of Zoledronic Acid in Preventing Collapse of the Osteonecrotic Femoral Head Phase III: RCT, safety/efficacy study NCT00939900 Evaluate the Effect of Bone Marrow Derived Cd133+ Cells in Patient With Osteonecrosis of Femoral Head Phase I: Single group assignment, safety study NCT01198080 Bisphosphonates and Impaction Grafting in Hip Revision Phase II: RCT, efficacy study NCT00658268 Efficacy and safety of autologous conditioned serum (ACS/Orthokine®) compared with Triamcinolone in the treatment of symptomatic hip osteoarthritis. RCT, safety/efficacy study ISRCTN16719506 Perioperative Pregabalin Use, Rehabilitation, Pain Outcomes and Anxiety Following Hip Surgery Phase IV: RCT NCT00762099 Transversalis Fascial Plane Nerve Block in Iliac Crest Bone Graft RCT, efficacy study NCT01133730 Biological: cell injection Hip Osteoarthritis Rec 6 Adt Mar-11 Jun-13 Royan Institute http://ClinicalTrials.gov/show/NCT01500811 Drug: zoledronic acid Avascular Necrosis (aclasta) of Femoral Head Rec 104 Adt Jul-09 Dec-12 Seoul National University Bundang Hospital; Novartis Korea Ltd. Adt Aug-09 May-12 Royan Institute http://ClinicalTrials.gov/show/NCT00939900 Biological: CD133+ cells Osteonecrosis Rec 10 Drug: Clodronate; Drug: Placebo Aseptic Loosening of the Hip Prosthesis Rec 32 Adt Mar-08 Mar-12 Region Skane Sen http://ClinicalTrials.gov/show/NCT00658268 ACS / Orhtokin® injection; Tramcinolone injection Osteoarthritis of the hip Comp 130 Adt Mar-10 Dec-11 Orthogen AG Sen (Germany) http://www.controlledtrials.com/ISRCTN16719506 Drug: Pregabalin; Drug: Placebo Anxiety Rec 184 Adt May-09 Dec-11 Sunnybrook http://ClinicalTrials.gov/show/NCT00762099 Sen Health Sciences Centre; Pfizer Drug: Active treatment; Drug: Placebo Arm Upper Limb Surgery; Not yet Iliac Crest Bone Rec Harvest 56 Adt Aug-10 Nov-11 University Health http://ClinicalTrials.gov/show/NCT01133730 Sen Network, Toronto 204 http://ClinicalTrials.gov/show/NCT01198080 Treatment of early stage osteonecrosis of the femoral head with implantation of autologous bone marrow-derived and cultured mesenchymal stem cells RCT ISRCTN18167626 Bone marrowOsteonecrosis of the Comp derived femoral head at mesenchymal stem early stage cell; utologous bone marrow mononuclear cells 100 Adt Mar-04 Sep-11 Dalian University http://www.controlledZhongshan trials.com/ISRCTN18167626 Hospital (China) Memantine for Post-Operative Pain Control Phase IV: RCT, safety/efficacy study NCT01041313 Antiemetic Prophylaxis for Postdischarge Nausea and Vomiting After Hip Arthroscopy Phase IV: RCT, efficacy study NCT00878228 Efficacy of Zoledronic Acid in Enhancement of Early Stability of Cementless Primary Hip Prosthesis Phase IV: RCT, efficacy study NCT01218035 Mesenchymal Stem Cell Transplantation in Osteoarthritis of Hip Joint Phase I: Single group assignment, safety study NCT01499056 Steroid versus hyaluronic acid injections for hip arthritis RCT ISRCTN04950164 Drug: Memantine; Drug: Placebo Rec 120 Adt Jan-10 Sep-11 University of Sen Washington; Forest Laboratories Drug: Ondansetron; Nausea and Drug: Placebo Vomiting, Postoperative Active, NR 76 Adt Drug: zoledronic acid Hip Osteoarthritis Comp 49 Biological: stem cell Hip Osteoarthritis injection Comp 6 Adt May-07 Jun-11 Turku University http://ClinicalTrials.gov/show/NCT01218035 Sen Hospital; Academy of FFinland; only Novartis; Stryker Nordic Adt Jun-10 Mar-11 Royan Institute http://ClinicalTrials.gov/show/NCT01499056 Kenalog® Hip osteoarthritis (triamcinolone) intraarticular injection; Hyaluronic acid intraarticular injection Comp Pain, Post-operative; THR; TKR; lumbar spinal fusion http://ClinicalTrials.gov/show/NCT01041313 Apr-09 Aug-11 Hospital for http://ClinicalTrials.gov/show/NCT00878228 Special Surgery, New York 110 Child Jul-09 Dec-10 Dorset County http://www.controlledAdt Hospital NHS trials.com/ISRCTN04950164 Sen Foundation Trust (UK) 205 Modulation of the Surgical Inflammatory Response by Etoricoxib Phase II: RCT, pharmacokinetics/dynamics study NCT00746720 Drug: Etoricoxib 60 Pain; Osteoarthritis, mg; Drug: Placebo Hip; Analgesia for Etoricoxib 60 mg; Drug: Etoricoxib 60 mg; Drug: Placebo for Etoricoxib 60 mg Postoperative Analgesia With Drug: Ropivacaine; Local Infiltration After Drug: Placebo Periacetabular Osteotomy Phase IV: RCT, safety/efficacy study NCT00815503 Effect of Local Administration of Drug: morphine Morphine for Analgesia After Iliac Bone Graft Harvest Phase IV: RCT NCT01037335 Procedure Pivotal, Multicentre, Randomised, Procedure: Core Double-blind Controlled Study to decompression Evaluate the Efficacy and Safety of Autologous Osteoblastic Cells (PREOB®) Implantation in Early Stage Non Traumatic Osteonecrosis of the Femoral Head Phase III: RCT, safety/efficacy study NCT01529008 Hip Impingement - Understanding Procedure: MRI, Cartilage Damage qCT, motion Non-randomized, parallel analysis; Procedure: assignment MRI, qCT, motion NCT01546493 analysis; Procedure: MRI, qCT, motion analysis Term 52 Periacetabular Osteotomy; Pain Comp 70 Autogenous Bone Grafts Rec 60 Adt Apr-09 Mar-10 Outcomes http://ClinicalTrials.gov/show/NCT01037335 Sen Research Consortium; The Cleveland Clinic; Haydarpasa Numune Training and Research Hospital Avascular Necrosis of Femur Head Rec 130 Adt Nov-11 Nov-16 Bone Therapeutics S.A Femoroacetabular Impingement Rec 75 Adt Sep-10 Sep-15 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01546493 Sen Research Institute; Canadian Institutes of Health Research 206 Adt May-06 Dec-10 University of http://ClinicalTrials.gov/show/NCT00746720 Sen ErlangenNürnberg Medical School; HELIOS Kliniken GmbH; Rush University Medical Center; Merck Adt Jan-09 Dec-10 Odense http://ClinicalTrials.gov/show/NCT00815503 Sen University Hospital http://ClinicalTrials.gov/show/NCT01529008 UK FASHIoN: Feasibility study of a Hip Arthroscopic Femoroacetabular Active trial of Arthroscopic Surgery for Hip Surgery; Nonimpingement (FAI) Impingement compared with Non- operative care operative care RCT ISRCTN09754699 Efficacy and Patient Satisfaction Procedure: Postop Wound Healing; Rec With AQUACEL® Ag Surgical Dressing; Procedure: TKA; THA Dressing Compared to Standard Postop Dressing Surgical Dressing RCT, safety/efficacy study NCT01258270 Acetabular Labral Tear in Procedure: labrum Developmental Rec Dysplastic Hips Dysplasia of the Hip; Prospective, case control study Labrum NCT01345838 The Effect of Perthes' Disease on Procedure: MRI Perthes' Disease Susp Hip Cartilage Cross-sectional, case-only study NCT00958464 Movement Pattern in Patients With Procedure: Minimally Hip Dysplasia Rec Hip Dysplasia invasive approach for Prospective, cohort study Periacetabular NCT01344421 osteotomy Dynamic Imaging of the Hip for Procedure: Motion Femoroacetabular, Active, Pre-operative Planning analysis; Procedure: Impingement NR Non-randomized, parallel Motion analysis assignment NCT00605969 Identification of Microcirculation Procedure: PCCP; Level of Pain Rec and Inflammation After MinimalProcedure: DHS; invasive Osteosynthesis of the Procedure: Proximal Femur Osteosynthesis with RCT nails NCT01264172 Local Infiltration Analgesia for Hip Procedure: Infiltration Pain Rec Arthroscopy of local anesthetic; RCT, efficacy study Procedure: Normal NCT01454518 Saline Injection 60 Adt Mar-12 Sep-13 University Hospitals Coventry & Warwickshire (UK) http://www.controlledtrials.com/ISRCTN09754699 300 Adt Dec-10 Aug-13 OrthoCarolina Sen Research Institute, Inc.; ConvaTec Inc. http://ClinicalTrials.gov/show/NCT01258270 100 Child Feb-10 Jun-13 University of Adt Aarhus Sen 20 http://ClinicalTrials.gov/show/NCT01345838 Child Jan-08 Apr-13 University of http://ClinicalTrials.gov/show/NCT00958464 Adt British Columbia 60 Adt Mar-11 Jan-13 Aarhus University Hospital 30 Adt May-07 Dec-12 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00605969 Research Institute 90 Adt Dec-10 Dec-12 RWTH Aachen Sen University http://ClinicalTrials.gov/show/NCT01264172 36 Adt Oct-11 Sep-12 Saint Francis Sen Care http://ClinicalTrials.gov/show/NCT01454518 207 http://ClinicalTrials.gov/show/NCT01344421 The Effect of a Pre- and Postoperative Orthogeriatric Service RCT, efficacy study NCT01009268 Procedure: Orthogeriatric intervention Dementia; Delirium Rec Osteoarthritis; TKA; Procedure: PeriRec articular injection of THA marcaine/epinephrin e; Procedure: Periarticular injection of marcaine alone Retrospective Follow-up Study Procedure: Follow-up Congenital Deformity Comp After Periacetabular Osteotomy in of Hip Joints Adults Retrospective, cohort study NCT01348178 Bone Repair Cell (BRC) Treatment Procedure: Core Osteonecrosis Active, of Patients With Osteonecrosis of decompression NR the Femoral Head Phase III: RCT, safety/efficacy study NCT00505219 Lumbar Plexus Block for Procedure: Lumbar Postoperative Pain Active, Postoperative Pain Control After Plexus Blockade; NR Hip Arthroscopy. A Randomized Procedure: Control Controlled Trial Phase IV: RCT NCT01286805 Controlled Study of Stage 3 Procedure: core Non Traumatic Comp Osteonecrosis Treatment by Bone decompression with Osteonecrosis of the Marrow autologous bone Femoral Head (Hip) RCT, safety/efficacy study marrow implantation; NCT01544712 Procedure: core decompression of the femoral head Local Analgesia in Knee- and Procedure: Position Rheumatoid Arthritis; Rec Hipatroplastic Surgery in Patients of catheter Orthopedic Surgery; With Rheumatic Disease: ExtraAnalgesia vs. Intracapsulare Position of Catheter RCT, efficacy study NCT01050738 Study Comparing Peri-articular Injection of Bupivacaine With and Without Epinephrine RCT, efficacy study NCT00737139 400 Child Sep-09 Sep-12 Ullevaal http://ClinicalTrials.gov/show/NCT01009268 Adt University Sen Hospital; The Research Council of Norway 240 Adt Sep-08 Sep-12 Rush University http://ClinicalTrials.gov/show/NCT00737139 Sen Medical Center 401 Child Mar-10 Nov-11 University of Adt Aarhus Sen http://ClinicalTrials.gov/show/NCT01348178 120 Adt Sep-07 Jun-11 Aastrom Sen Biosciences http://ClinicalTrials.gov/show/NCT00505219 82 Adt May-10 May-11 Hospital for http://ClinicalTrials.gov/show/NCT01286805 Special Surgery, New York; New York Presbyterian Hospital Adt Aug-04 Sep-10 University http://ClinicalTrials.gov/show/NCT01544712 Sen Hospital of Liege 50 72 208 Child Jan-10 Aug-10 Spenshult Adt Hospital Sen http://ClinicalTrials.gov/show/NCT01050738 Other Shared Decision Making in Other: Shared Patients With Osteoarthritis of the Decision Making Hip and Knee Intervention RCT NCT01492257 Galileo-Hip Whole Body Vibration /Conventional Physiotherapy /Coxarthrosis Phase IV: RCT, efficacy study NCT01279174 Do Hip Injections Improve ShortTerm Biomechanical Outcomes In Patients With Hip Pain Prospective, case-only study NCT01390103 Exercise Therapy and Patient Education for Individuals With Hip Osteoarthritis. Long-term Followup. RCT, efficacy study NCT01063777 Conservative Treatment for Hip Osteoarthritis RCT, efficacy study NCT01039337 Rec 120 Not yet Rec 40 Rec Other: A 12 week Hip Osteoarthritis exercise therapy program and patient education.; Other: Patient education Other: Hip School; Other: Hip School and Manual Treatment; Other: Minimal control intervention Other: Conventional Coxarthrosis physiotherapy Other: Assessment Hip Pain following hip injection Miscellaneous observational studies A Clinical Investigation of the M2aMagnum™ Hip System Prospective, cohort study NCT00698347 Outcome in Hip Preservation Patients Prospective, cohort study NCT01550263 Hip Osteoarthritis; Knee Osteoarthritis Osteoarthritis, Hip Jul-14 University of California, San Francisco; Stanford University; Robert Wood Johnson Foundation Adt Apr-11 Oct-12 University of Sen Cologne http://ClinicalTrials.gov/show/NCT01492257 30 Adt Mar-11 Mar-12 University of Sen Florida http://ClinicalTrials.gov/show/NCT01390103 Active, NR 109 Adt Jan-09 Dec-11 Ullevaal Sen University Hospital http://ClinicalTrials.gov/show/NCT01063777 Active, NR 120 Adt Oct-08 Jun-11 Nordic Institute Sen of Chiropractic and Clinical Biomechanics (Denmark) http://ClinicalTrials.gov/show/NCT01039337 Osteoarthritis, Hip; Active, Arthritis; Rheumatoid NR Arthritis; Joint Disease; Bone Disease Hip Pain Invite Adt Sen Jul-11 http://ClinicalTrials.gov/show/NCT01279174 249 Child Nov-04 Nov-18 Biomet Adt Orthopedics, Sen LLC http://ClinicalTrials.gov/show/NCT00698347 200 http://ClinicalTrials.gov/show/NCT01550263 209 Adt Jan-12 Jan-18 University of Sen Utah Mini Stem Radiostereometric Analysis Study Prospective, cohort study NCT01064531 A Clinical Investigation of the Taperloc® Microplasty™ Hip System Prospective, cohort study NCT00699309 Mini Stem DEXA (Dual Energy Xray Absorptiometry) Prospective, cohort study NCT01066936 Discovering the Gene(s) Causing Developmental Dysplasia of the Hip Cross-sectional, case-only study NCT01193673 R3® Acetabular System in Patients With Degenerative Hip Disease Prospective study NCT01407029 A Clinical Investigation of the Balance® Microplasty™ Hip System Prospective, cohort study NCT00699088 Systemic Effects of Chronic Metal Ion Exposure From Metal-on Metal Hip Resurfacing Prospective, cohort study NCT01493141 Osteoarthritis, Hip 4 Child Jun-09 Sep-15 Smith & Adt Nephew, Inc. Sen http://ClinicalTrials.gov/show/NCT01064531 Osteoarthritis; Active, Rheumatoid Arthritis; NR Avascular Necrosis 98 Adt Aug-05 Jun-15 Biomet Sen Orthopedics, LLC http://ClinicalTrials.gov/show/NCT00699309 Osteoarthritis, Hip 20 Child Aug-09 Apr-15 Smith & Adt Nephew, Inc. Sen http://ClinicalTrials.gov/show/NCT01066936 Focus on Patients Who Have Hip Dysplasia and Their Family Rec Rec 200 Child Jan-10 Jan-15 University of Adt Utah Sen http://ClinicalTrials.gov/show/NCT01193673 158 Adt Oct-09 Dec-14 Smith & Sen Nephew, Inc. http://ClinicalTrials.gov/show/NCT01407029 Osteoarthritis, Hip; Active, Rheumatoid Arthritis; NR Avascular Necrosis 70 Adt Jan-05 Jun-14 Biomet Sen Orthopedics, LLC http://ClinicalTrials.gov/show/NCT00699088 Osteoarthritis 70 Adt Nov-09 Apr-14 Sheffield http://ClinicalTrials.gov/show/NCT01493141 Sen Teaching Hospitals NHS Foundation Trust; NIHR Biomedical Research Unit for Musculoskeletal Disease Osteoarthritis Active, NR Rec Active, NR 210 Genetic Factors Affecting Risks for Rotator Cuff Disease Cross-sectional, case-only study NCT01193647 THRA_hematologic Variables Retrospective, case-only study NCT01521858 Studying the Genetic Invite Relationship of Rotator Cuff Tears 400 Adt Sen Avascular Necrosis of Hip Rec 73 Measured Hypocretin Levels and Recovery After Hip Surgery Prospective, case-only study NCT01009710 Psychological, Sexually and Social Consequences of Osteoarthritis Treatment With THA or TKA and Joint Preserving Surgery Prospective, cohort study NCT01305759 Osteoarthritis, Hip Invite 50 Adt Jan-12 Jan-13 Seoul National Sen University Bundang Hospital Adt Jul-09 Nov-12 Stanford Sen University Total Hip Registry Prospective, cohort study NCT01133249 Osteoarthritis Study of Brain and Spinal Cord Tumor Growth and Cyst Development in Patients With Von Hippel Lindau Disease NCT00005902 Avascular Necrosis (AVN) LongTerm Follow-up NCT00833430 Digital Sizing for Orthopaedic Hip Implants Prospective, case-only study NCT00665210 Hemangioblastoma; Hippel Lindau Disease Active, NR Avascular Necrosis; Femoral Head Collapse Hip Arthritis Term 35 Rec 100 Child Oct-07 Oct-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00665210 Adt Research Sen Institute Osteoarthritis; Depression; Hip Dysplasia Active, NR Invite Jul-09 Jul-13 University of Utah http://ClinicalTrials.gov/show/NCT01193647 http://ClinicalTrials.gov/show/NCT01521858 http://ClinicalTrials.gov/show/NCT01009710 250 Child Apr-10 Apr-12 Hvidovre http://ClinicalTrials.gov/show/NCT01305759 Adt University Hospital; Frederiksberg University Hospital; Aarhus University Hospital; University Hospital Koge 942 Adt Jul-05 Feb-12 Heekin http://ClinicalTrials.gov/show/NCT01133249 Sen Orthopedic Research Institute; Stryker Orthopaedics; DePuy Orthopaedics; ConforMIS, Inc. 250 Child Jun-00 Jan-12 National Institute http://ClinicalTrials.gov/show/NCT00005902 Adt of Neurological Sen Disorders and Stroke (NINDS) 211 Adt Jun-06 Dec-11 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT00833430 Clinical Outcome of Birmingham Hip Resurfacing (BHR) Using VISIONAIRE Femoral Alignment Guide Prospective study NCT01427361 Osteoarthritis Rec 25 Mesenchymal Stromal Cells and Osteoarthritis Prospective, case control study NCT01038596 Osteoarthritis Rec 30 Modified Triple Osteotomy for Acetabular Dysplasia Retrospective, case-only study NCT01285154 Sharp Angle; Center Rec Edge Angle; Femoral Head Extrusion Index; Center Head Distance Discrepancy Staphylococcal Not yet Infections; Rec Prosthesis; hip, knee and shoulder Prosthetic Joint Infection (PJI) Daptomycin With Rifampin for Treatment of Staphylococcal Prosthetic Joint Infection Prospective, cohort study NCT01144000 Predictive Factors for the Development of Osteonecrosis After the Treatment of the Developmental Dislocated Hip Retrospective, cohort study NCT01133938 Predictors of Comp Osteonecrosis of the Femoral Head After Treatment of the Dislocated Hip 2 60 79 212 Adt Oct-09 Aug-11 Smith & http://ClinicalTrials.gov/show/NCT01427361 Sen Nephew, Inc.; Jason Jones, MS, Group Director, Clinical Affairs, Smith&Nephew Adt Jan-09 Jun-11 Dresden http://ClinicalTrials.gov/show/NCT01038596 Sen University of Technology; German Federal Ministry of Education and Research; Center for Regenerative Therapies Dresden (CRTD) Child Feb-11 Jun-11 National Taiwan http://ClinicalTrials.gov/show/NCT01285154 Adt University Sen Hospital Adt Sep-10 Jun-11 Centre http://ClinicalTrials.gov/show/NCT01144000 Sen Hospitalier Universitaire Vaudois; University of Lausanne Hospitals; Kantonsspital Liestal; Schulthess Klinik Child Jan-09 May-10 Orthopedic http://ClinicalTrials.gov/show/NCT01133938 Hospital Vienna Speising A9. KNEE A9A: PAEDIATRICS Title Phases: trial design (control) CT ID Device Stapling Versus 8plate for Correction of Genu Valgus RCT, safety/efficacy study NCT01528553 Efficacy of Instrumental Chiropractic Treatment Using Activator Methods for Pain and Dysfunction in Juvenile Athletes RCT, efficacy study NCT01449994 Interventions Conditions Recruit n Age Start (Grp) Date Device: 8plate; Device: Staples (Richards, Smith & Nephew) Device: Activator IV (Activator Methods Int. Phoenix, Arizona) Deformity; Genu Valgus Active NR 20 Child Aug-09 Aug-12 University of Aarhus http://ClinicalTrials.gov/show/NCT01528553 Pain in Leg, Unspecified; Knee Sprain Comp 26 Child Jul-10 Feb-12 Medical University of Graz http://ClinicalTrials.gov/show/NCT01449994 50 Child Dec-10 Apr-13 University of http://ClinicalTrials.gov/show/NCT00175630 British Columbia 64 Child Dec-09 Apr-12 Capio Research http://www.controlledFoundation trials.com/ISRCTN39959729 (Sweden) Procedure The Effect of Femoral Nerve Block Procedure: Pain, Postoperative Rec on Postoperative Opioid Use After Administration of a Anterior Cruciate Ligament (ACL) femoral nerve block Reconstruction (bupivacaine HCL) Phase I: RCT, safety/efficacy study NCT00175630 Conservative versus arthroscopic Conservative Dislocation of Patella Active refixation of the Medial (orthosis) treatment; PatelloFemoral Ligament (MPFL) arthroscopic after traumatic first time dislocation refixation of the of the patella in children MPFL with the use of RCT, efficacy study anchors ISRCTN39959729 213 End Sponsors Date URL A9B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Procedure Effect of Low-Magnitude, High Frequency Vibration Treatment on Femoral Shaft Fracture Healing Phase II/III: RCT, efficacy studyNCT01386749 Interventions Conditions Recruit n Rec 50 Adt Feb-11 Dec-13 Chinese University of Hong Kong Intra-articular Knee Fractures Active, NR 40 Adt Dec-06 Mar-12 Greenville http://ClinicalTrials.gov/show/NCT00591929 Sen Hospital System University Medical Center; Orthopaedic Trauma Association Conditions Recruit n Rec 60 Procedure: vibration Fracture, Closed, platform provide low Comminuted, magnitude and high Healing frequency vibration treatment, which is self-developed by our research team Other Use of Continuous Passive Motion Other: Continuous in the Post-Operative Treatment of Passive Motion Intra-articular Knee Fractures RCT NCT00591929 Age Start (Grp) Date End Sponsors Date URL http://ClinicalTrials.gov/show/NCT01386749 A9C: ARTHROSCOPY Title Phases: trial design (control) CT ID Device Intra-articular Hyaluronan After Arthroscopic Meniscal Surgery RCT, safety/efficacy study NCT01482624 Interventions Device: Hyaluronan Arthroscopic (0.5%, 5 mg/10 ml); Meniscal Surgery Procedure: Standard arthroscopic meniscal surgery 214 Age Start (Grp) Date End Sponsors Date URL Adt Dec-11 Jan-13 TRB Chemedica http://ClinicalTrials.gov/show/NCT01482624 Sen AG Autologous Chondrocyte Device: Arthroscopic Tear; Knee, Transplantation For Articular matrix encapsulated Cartilage, Articular Cartilage Regeneration chondrocyte Phase I/II: Single group implantation assignment, safety/efficacy study NCT01503970 The treatment of medial KineSpring™ Medial Knee OA compartmental knee osteoarthritis Unicompartmental (OA) symptoms with the Knee Arthroplasty KineSpring™ Unicompartmental (UKA) System Knee Arthroplasty (UKA) System Single group assignment (historical control) ISRCTN63048529 A Prospective Randomized Study Device: Vanguard Total Knee on Vanguard Cruciate Retaining PS Knee; Device: Arthroplasty Versus Vanguard High Flex Vanguard CR Knee Posterior Stabilized Total Knee System in the Early Range of Motion RCT, safety/efficacy study NCT00763113 Effects of TENS Therapy Following Device: TENS Meniscus Tear Arthroscopic Knee Surgery Treatment with RCT, efficacy study functional or disabled NCT01528228 unit Temperature Sensitive Release of Device: Cooling and Knee Arthroscopy; PGE2 and Diminished Energy compression Meniscus; Requirements in Synovial Tissue Inflammation; With Postoperative Cryotherapy Hydrops; Cooling A Prospective Randomised Study After Knee Arthroscopy RCT, efficacy study NCT01247376 Active, NR 10 Adt Dec-08 Dec-12 Instituto http://ClinicalTrials.gov/show/NCT01503970 Nacional de MRehabilitacion; only National Council of Science and Technology, Mexico Adt Sep-09 Jun-12 Moximed Inc. http://www.controlledSen (USA) trials.com/ISRCTN63048529 Active 30 Active, NR 173 Child Jun-07 Jun-12 Biomet, Inc. Adt Sen http://ClinicalTrials.gov/show/NCT00763113 Invite 20 Adt Jul-11 Apr-12 A.T. Still http://ClinicalTrials.gov/show/NCT01528228 University of Health Sciences Comp 40 Adt Jan-08 Jun-10 Karolinska Institutet 215 http://ClinicalTrials.gov/show/NCT01247376 Comparison of a Pain Pump Versus Injectable Medication for Analgesia in Knee Arthroscopy Phase II: RCT NCT01242644 Device: pain pump Pain containing ropivacaine; Device: saline pain pump with injectable medication; Drug: ropivacaine, ketorolac , morphine sulfate Drugs including biologics Pot-Kast: Thrombosis Prophylaxis Drug: LMWH After Knee Arthroscopy RCT, efficacy study NCT01542723 Comp 49 Deep Venous Thrombosis; Pulmonary Embolism Adt Oct-06 Jun-10 University of http://ClinicalTrials.gov/show/NCT01242644 Sen South Alabama Not yet 1500 Adt Apr-12 Apr-16 Suzanne C. http://ClinicalTrials.gov/show/NCT01542723 Rec Sen Cannegieter, MD PhD; ZonMw: The Netherlands Organisation for Health Research and Development Autologous Tolerogenic Dendritic Drug: TolDC; Drug: Rheumatoid Arthritis Not yet 12 Adt Aug-11 Aug-13 Newcastle http://ClinicalTrials.gov/show/NCT01352858 Cells for Rheumatoid Arthritis Arthroscopy & saline Rec Sen University; (AutoDECRA) irrigation alone Arthritis Phase I: RCT, safety study Research UK NCT01352858 (funder); Newcastle-uponTyne Hospitals NHS Trust Safety and Efficacy of Drug: OMS103HP-S; Meniscal Tear Rec 330 Adt Aug-11 Jun-12 Omeros http://ClinicalTrials.gov/show/NCT01406561 OMS103HP-S Administered in Drug: Vehicle Sen Corporation Joint Irrigation Solution to Subjects Undergoing Arthroscopic Meniscectomy Phase III: RCT, safety/efficacy study NCT01406561 Safety and Effectiveness of Drug: extendedPostoperative Pain Not yet 100 Adt Dec-09 Dec-11 Shaare Zedek http://ClinicalTrials.gov/show/NCT01024348 Tramadex-OD After Knee release tramadol; Rec Medical Center Arthroscopy Drug: paracetamol RCT, safety/efficacy study NCT01024348 216 Infrapatellar Nerve Block for Postoperative Knee Arthroscopy Pain Control Phase IV: RCT, efficacy study NCT01279447 Selective Unilateral Spinal Anesthesia Versus Selective Sensory Spinal Anesthesia for Knee Arthroscopy Surgery Phase IV: RCT, safety/efficacy study NCT01356797 The Analgesic Effect of Intrathecal Hydromorphone Injection on Spinal Anesthesia RCT, efficacy study NCT01172782 Procedure Development of Knee Osteoarthritis After Arthroscopic Partial Resection of Degenerative Meniscus Tear Phase IV: RCT, efficacy study NCT01052233 Surgical or Exercise Therapy on Patients With Degenerative Meniscus Tears NCT01002794 Drug: 0.25% Bupivacaine; Drug: Normal Saline Knee Pain; Knee Derangement Syndrome; Knee Arthroscopy Rec 70 Adt Jan-11 Oct-11 Northwestern Sen University Drug: hypobaric Pain levobupivacaine with fentanyl; Drug: hyperbaric bupivacaine 0,5% Comp 54 Adt May-11 Sep-11 USP Hospital La http://ClinicalTrials.gov/show/NCT01356797 Sen Colina Drug: Hydromorphone Pain Measurement; Visual Analog Pain Scale; knee arthroscopic surgery Comp 60 Adt Sen Procedure: Arthroscopic partial meniscectomy; Procedure: Arthroscopy (diagnostic) Osteoarthritis of the Knee; Arthroscopy; Meniscal Tear Rec 160 Adt 340 Adt May-08 Aug-16 Brigham and Sen Women's Hospital Procedure: Degenerative Arthroscopic partial Meniscus Tear menisectomy; Other: Supervised neuromuscular and strength training Comparing Knee Cartilage Surgery Procedure: Osteoarthritis Versus Standard Physical Therapy Arthroscopic partial in Treating People With a Meniscal menisectomy; Other: Tear and Osteoarthritis Standard physical Phase II: RCT therapy; Other: NCT00597012 Postoperative rehabilitative physical therapy Rec Active, NR 217 Jul-09 http://ClinicalTrials.gov/show/NCT01279447 Jul-10 Korea University http://ClinicalTrials.gov/show/NCT01172782 Anam Hospital; Korea University Jan-10 Jan-24 University of http://ClinicalTrials.gov/show/NCT01052233 Tampere; Helsinki University Central Hospital; Turku University Hospital; Kuopio University Hospital; Central Finland Hospital District Adt Nov-09 Dec-16 Oslo University http://ClinicalTrials.gov/show/NCT01002794 Hospital; University of Southern Denmark http://ClinicalTrials.gov/show/NCT00597012 The Benefit of Arthroscopic Partial Meniscectomy in Middle-Aged Patients RCT, efficacy study NCT01264991 Arthroscopic Debridement for Chondral Lesions in the Knee RCT NCT01527201 Arthroscopy in the Treatment of Degenerative Medial Meniscus Tear Phase II/III: RCT, efficacy study NCT00549172 Procedure: Arthroscopic partial meniscectomy; Procedure: Sham procedure Procedure: Arthroscopic debridement Degenerative Meniscus Tear Rec 150 Meniscal Tear; Chondromalacia Rec 190 Active, NR 140 Rec 150 Rec 72 Adt Nov-10 Apr-12 Glostrup Sen University Hospital, Copenhagen Active, NR 10 Comp 21 Adt Feb-06 Feb-12 State University http://ClinicalTrials.gov/show/NCT00643487 Sen of New York Upstate Medical University Adt Jun-11 Jan-12 Northern http://ClinicalTrials.gov/show/NCT01509729 Sen Orthopaedic Division, Denmark Procedure: Operative Degenerative Tear (partial arthroscopy); of the Medial Procedure: Meniscus of Knee Conservative (diagnostic arthroscopy) Is a Knee Arthroscopy of Any Procedure: Knee Injury;Meniscus;Chr Benefit for the Middleaged Patient arthroscopy onic With Meniscal Symptoms? RCT, efficacy study NCT01288768 The Efficacy of Adductor-CanalProcedure: Adductor- Meniscus Lesion; Block (ACB) in Patients After Knee Canal-Block, Pain (Knee); Arthroscopy Ropivacain; Diagnostic Knee Phase IV: RCT, safety/efficacy Procedure: Adductor Artroscopy; Minor study Canal Block, Placebo Knee Surgery NCT01254825 (saline) In Vivo Arthroscopic Behavior of Procedure: Patellofemoral Pain the Infrapatellar Plica of the Knee observation of the Syndrome Prospective, case-only study behavior of the NCT00643487 infrapatellar plica Topical Lidocaine After Major Procedure: Sham Fracture of Patella; Arthroscopic Knee Surgery operation; Pain RCT, efficacy study Procedure: Knee NCT01509729 arthroscopic surgery 218 Adt Dec-10 Nov-15 Slagelse http://ClinicalTrials.gov/show/NCT01264991 Hospital; University of Southern Denmark Adt Jan-12 Jan-15 State University http://ClinicalTrials.gov/show/NCT01527201 Sen of New York at Buffalo Adt Oct-07 Jan-14 University of http://ClinicalTrials.gov/show/NCT00549172 Tampere; Helsinki University Central Hospital; Kuopio University Hospital; Turku University Hospital; Central Finland Hospital District Adt Mar-10 Dec-12 University http://ClinicalTrials.gov/show/NCT01288768 Hospital, Linkoeping http://ClinicalTrials.gov/show/NCT01254825 HTO With and Without Arthroscopy Phase II: RCT, safety/efficacy study NCT00284622 Evaluation of MRI Diagnosed Meniscal Lesions RCT, safety/efficacy study NCT01492855 Procedure: Arthroscopy Medial Compartment Not yet Osteoarthritis of the Rec Knee 98 Adt Dec-09 Dec-11 Fowler Kennedy http://ClinicalTrials.gov/show/NCT00284622 Sen Sport Medicine Clinic Procedure: Arthroscopy; Behavioral: Noninvasive treatment Meniscus Lesion Comp 324 Adt Jan-08 Dec-10 Northern Sen Orthopaedic Division, Denmark Rec 30 Adt May-11 May-11 University of http://ClinicalTrials.gov/show/NCT01359553 Sen Oulu; Oulu University Hospital; University of Eastern Finland; Kuopio University Hospital Term 32 Adt May-08 May-10 National Institute http://ClinicalTrials.gov/show/NCT00752271 Sen on Aging (NIA) Other Clinical Study of Novel Diagnostic Other: Intra-articular Knee Osteoarthritis; Techniques for Knee Osteoarthritis ultrasound imaging Knee Injuries Cross-sectional, case-only of knee joint during study arthroscopy; Other: NCT01359553 Non-invasive ultrasound imaging of knee; Other: Quantitative MRI imaging of knee; Other: Contrastenhanced CT imaging of knee Miscellaneous observational studies AMS Study: Inflammatory and Biomechanical Contributors to Arthritis Development Following Arthroscopic Meniscectomy Prospective, case control study NCT00752271 Osteoarthritis 219 http://ClinicalTrials.gov/show/NCT01492855 A9D: CRUCIATE LIGAMENT PATHOLOGIES Title Interventions Phases: trial design (control) CT ID Device Safety and Efficacy Study of the Z- Device: Z-Lig; Lig Medical Device Compared to Device: Allograft Allograft RCT, safety/efficacy study NCT01245400 Conditions Recruit n Age Start (Grp) Date Ruptured Anterior Cruciate Ligaments Rec 60 Safety and Efficacy of the Knee-T- Device: Knee-T-Nol Anterior Cruciate nol Anterior Cruciate Ligament Ligament Rupture (ACL) Prosthesis Single group assignment, safety/efficacy study NCT01450332 Therapeutic Effects of Cryotherapy Device: cryotherapy Anterior Cruciate and Transcutaneus Nerves Ligament Injury Stimulation on Arthrogenic Muscle Inhibition in Patients With Anterior Cruciate Ligament Reconstruction Single group assignment NCT01273649 Evaluation of Biocleanse Allografts Device: ACL Cruciate Ligament, For ACL Reconstruction reconstruction Anterior; Allograft Phase IV: Prospective, caseonly study NCT00187876 Weight-bearing Measuring Device Device: Smart_Step Weight-bearing Following Anterior Cruciate weight bearing insole Deficits Ligament Reconstruction Phase I: Single group assignment, efficacy study NCT01127685 Rec 20 Adt Nov-10 Aug-13 Aperion Biologics, Inc.; MedPass International; Contract Research Organization Adt Mar-11 Jan-13 Tavor Ltd. Rec 30 Adt Monly End Sponsors Date URL http://ClinicalTrials.gov/show/NCT01245400 http://ClinicalTrials.gov/show/NCT01450332 Jan-11 Dec-11 National Taiwan http://ClinicalTrials.gov/show/NCT01273649 University Hospital Comp 138 Adt Feb-04 Jul-11 University of Florida http://ClinicalTrials.gov/show/NCT00187876 Comp 30 Adt May-10 Jul-11 Meir Medical Sen Center http://ClinicalTrials.gov/show/NCT01127685 220 SeriACL™ Device (Gen IB) Trial for Anterior Cruciate Ligament (ACL) Repair Phase I/II: Single group assignment, safety/efficacy study NCT00775892 Triathlon Cruciate Retaining (CR) Outcomes Study Single group assignment NCT00957723 Device: SeriACL Device ACL Reconstruction Anterior Cruciate Ligament Reconstruction Comp 30 Adt Sep-08 May-10 Serica Technologies, Inc. http://ClinicalTrials.gov/show/NCT00775892 Device: Triathlon (CR) Total Knee System Arthropathy of Knee Joint; Osteoarthritis, Knee; Avascular Necrosis of Bone Active, NR 500 Adt Feb-05 Apr-10 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00957723 Anterior Cruciate Ligament Injury; Osteoarthritis Rec 24 Adt Mar-09 Jun-14 Mesoblast, Ltd. http://ClinicalTrials.gov/show/NCT01088191 Pain Rec 120 Adt Feb-09 Apr-13 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01186887 Sen Research Institute; Pfizer Rupture of the Anterior Cruciate Ligament With Instability of the Knee Joint. Rec 75 Adt Sen Drugs including biologics Safety and Efficacy Study of MSB- Biological: MSBCAR001 in Subjects 6 Weeks Post CAR001 Combined an Anterior Cruciate Ligament With Hyaluronan; Reconstruction Drug: Hyaluronan Phase I/II: RCT, safety/efficacy study NCT01088191 A Trial Assessing the Outcome of Drug: Celecoxib; Celecoxib Administration Versus Drug: Placebo Placebo Following Anterior Cruciate Ligament (ACL) Reconstruction RCT, efficacy study NCT01186887 Evaluation of Arthroscopic Drug: injection in the Reconstruction of the Anterior knee joint with 20 ml Cruciate Ligament by One Night of chirocaine Hospital Stay or by Day Surgery: a 0.125%; Drug: Randomised, Prospective Clinical injection in the knee Trial joint with 20 ml of Phase IV: RCT physiological fluid NCT00620477 Efficacy and Safety of OMS103HP Drug: OMS103HP; in Patients Undergoing Allograft Drug: Vehicle Anterior Cruciate Ligament (ACL) Reconstruction Phase III: RCT, safety/efficacy study NCT00226759 Knee Injuries Comp Jul-08 Dec-11 University http://ClinicalTrials.gov/show/NCT00620477 Hospital, Ghent 280 Child Nov-04 Mar-11 Omeros Adt Corporation 221 http://ClinicalTrials.gov/show/NCT00226759 Efficacy and Safety of OMS103HP in Patients Undergoing Autograft Anterior Cruciate Ligament (ACL) Reconstruction Phase III: RCT, safety/efficacy study NCT00226772 Safety of OMS103HP in Patients Undergoing Anterior Cruciate Ligament (ACL) Reconstruction Phase III: RCT, safety study NCT00245271 Perioperative Administration of Pregabalin in Patients Undergoing Arthroscopic Anterior Cruciate Ligament Reconstruction Phase IV: RCT, safety/efficacy study NCT01242332 A Randomized, Double Blind, Placebo-controlled Study to Assess the the Preemptive Benefit of Etoricoxib in Patients Receiving Anterior Cruciate Ligament Reconstruction Phase IV: RCT, safety/efficacy study NCT00554346 Procedure Comparison of Three Methods for Anterior Cruciate Ligament Reconstruction RCT NCT00529958 Drug: OMS103HP; Drug: Vehicle Knee Injuries Comp 280 Child Jun-05 Mar-11 Omeros Adt Corporation http://ClinicalTrials.gov/show/NCT00226772 Drug: OMS103HP; Drug: Vehicle Anterior Cruciate Ligament Reconstruction Comp 480 Child Oct-04 Mar-11 Omeros Adt Corporation http://ClinicalTrials.gov/show/NCT00245271 Drug: Pregabalin Postoperative Pain Management Comp 60 http://ClinicalTrials.gov/show/NCT01242332 Drug: Arcoxia (Etoricoxib 90 mg/tablet) Post-operational Pain Comp 64 Procedure: Patellar Tendon; Procedure: Hamstring Tendon; Procedure: DoubleBundle Anterior Cruciate Ligament Rupture; Deficiency of Anterior Cruciate Ligament; Chronic Instability of Knee; Anterior Cruciate Ligament Injury Active, NR 231 Child Sep-07 Dec-20 University of Adt Calgary; Workers' Compensation Board - Alberta 222 Adt Aug-09 Oct-10 Prince of Songkla University Child May-08 Jun-10 National Taiwan http://ClinicalTrials.gov/show/NCT00554346 Adt University Hospital; Merck http://ClinicalTrials.gov/show/NCT00529958 Single- vs. Double-Bundle ACL Reconstruction Phase II: RCT, efficacy study NCT01319409 Procedure: Anatomic Anterior Cruciate Double-Bundle ACL Ligament Injury Reconstruction; Procedure: Anatomic Single-Bundle ACL Reconstruction Rec Anterior Cruciate Ligament Reconstruction: Residual Rotational Laxity for Single Versus Double Bundle Techniques RCT, efficacy study NCT01377129 Procedure: Single bundle anterior cruciate ligament reconstruction; Procedure: Double bundle anterior cruciate ligament reconstruction Procedure: ACL reconstruction Anterior Cruciate Ligament Injury Rec Anterior Cruciate Ligament; Injury Rec Comparison of Doubled Quadrupled Versus Quadrupled Allograft Tissue Constructs for Anterior Cruciate Ligament (ACL) Reconstruction RCT NCT01148784 Initial Graft Tension and ACL Surgery RCT, efficacy study NCT00434837 Femoral Neuropathy After Anterior Cruciate Ligament Reconstruction: Femoral Nerve Block vs Patientcontrolled Analgesia (PCA) RCT NCT01321138 Anterior Cruciate Ligament (ACL) Reconstruction Using Different Grafts and Surgical Techniques Phase IV: RCT NCT00300300 160 Child Mar-11 Feb-16 University of http://ClinicalTrials.gov/show/NCT01319409 Adt Pittsburgh; National Institute of Arthritis and Musculoskeletal and Skin Diseases 54 Adt Oct-11 Oct-15 Centre http://ClinicalTrials.gov/show/NCT01377129 Sen Hospitalier Universitaire de Nīmes 100 Adt Jun-10 Jun-14 Oregon Health Sen and Science University http://ClinicalTrials.gov/show/NCT01148784 Procedure: Initial Anterior Cruciate Active, graft tension during Ligament Rupture NR ACL reconstruction surgery Procedure: Femoral Femoral Neuropathy Rec nerve block; Procedure: PCA morphine 168 Child Feb-04 May-14 Rhode Island Adt Hospital (US) http://ClinicalTrials.gov/show/NCT00434837 120 Child Apr-11 Nov-13 Centre Adt Hospitalier Universitaire Vaudois http://ClinicalTrials.gov/show/NCT01321138 Procedure: Computer-assisted surgery 125 http://ClinicalTrials.gov/show/NCT00300300 Anterior Cruciate Ligament Reconstruction Susp 223 Adt Sep-09 Sep-13 Queen's University Anterior Cruciate Ligament (ACL) Reconstruction: Single Bundle Versus Double Bundle Phase IV: RCT NCT01025895 Procedure: acl reconstruction double bundle technique; Procedure: acle reconstruction single bundle technique Lumbar Plexus Catheter Versus Procedure: lumbar Femoral Nerve Catheter for plexus catheter; Postoperative Pain After Anterior Procedure: femoral Cruciate Ligament (ACL) Repair nerve catheter; RCT, efficacy study Procedure: singleNCT01068275 shot femoral block The effect of prehabilitation on the Prehabilitation outcome of anterior cruciate exercise group; ligament reconstruction standard pre- and RCT, efficacy study post-operative care ISRCTN60779921 Double Bundle Anterior Cruciate Procedure: Single Ligament Reconstruction Bundle; Procedure: RCT, efficacy study double bundle NCT01033188 Pain Evaluation After Anterior Procedure: “AllCruciate Ligament (ACL) inside"; Procedure: Ligamentoplasty “Classical technique" Phase IV: RCT NCT01448278 Single Bundle Anterior Cruciate Procedure: anterior Ligament Reconstruction in Active cruciate ligament Young Men reconstruction RCT NCT01533025 Comparison of Infiltration Procedure: Analgesia With Femoral Nerve applicationsite Block After Hamstrings Anterior Cruciate Ligament Reconstruction RCT, efficacy study NCT01260363 Anterior Cruciate Ligament Tear Postoperative Pain Not yet Rec Rec 60 Child Jan-10 Jan-13 Assaf-Harofeh Adt Medical Center http://ClinicalTrials.gov/show/NCT01025895 114 Child Apr-10 Sep-12 Seattle Adt Children's Hospital http://ClinicalTrials.gov/show/NCT01068275 30 Jan-11 Jun-12 Cappagh National MOrthopaedic only Hospital (Ireland) 150 Adt Nov-09 Jun-12 Ullevaal University Hospital http://www.controlledtrials.com/ISRCTN60779921 Anterior cruciate ligament tear Active Knee Instability Rec Arthroscopic Anterior Cruciate Ligament Reconstruction Rec 45 Adt Nov-10 May-12 Hôpital Sen Ambroise Paré http://ClinicalTrials.gov/show/NCT01448278 Anterior Cruciate Ligament Rupture Comp 72 Adt Aug-08 Jan-12 National Police Hospital Monly http://ClinicalTrials.gov/show/NCT01533025 Anterior Cruciate Ligament Recontruction Rec 60 Adt Nov-10 Jan-12 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT01260363 224 Adt http://ClinicalTrials.gov/show/NCT01033188 Anterior Cruciate Ligament Reconstruction Using Single Bundle and Double Bundle Techniques RCT, efficacy study NCT01358656 Procedure: Single Anterior Cruciate bundle anterior Ligament Injury cruciate ligament reconstruction; Procedure: Double bundle anterior cruciate ligament reconstruction Preservation technique of ruptured Semitendinosus Ruptured Anterior anterior cruciate ligament (ACL) transplant; Dynamic Cruciate Ligament RCT, efficacy study intraligamentary ISRCTN89368687 stabilisation technique Use of Graft Tensioner Device in Procedure: ACL Torn Anterior ACL (Knee) Repair surgery Cruciate Ligament RCT, efficacy study (Knee) NCT00221273 The Efficacy of Adductor-CanalProcedure: Anterior Cruciate Block (ACB) in Patients After Ropivacain; Ligament Anterior Cruciate Ligament (ACL) Procedure: Saline Reconstruction Reconstruction Phase IV: RCT, efficacy study NCT01212666 Femoral Tunnel Position on Transtibial technique; Anterior Cruciate Conventional MRI After Anterior Transportal Ligament Rupture Cruciate Ligament Reconstruction- technique; anterior Transtibial Technique Versus cruciate ligament Transportal Technique reconstruction RCT, bio-equivalence study NCT01513434 Clinical Outcome of Posterior Procedure: PCL, Knee Injuries Cruciate Ligament (PCL) posterolateral Posterolateral Reconstruction reconstruction Single group assignment NCT00991588 Prospective Evaluation of Femoral Procedure: Sciatic Anterior Cruciate Versus Femoral and Sciatic Nerve Block; Procedure: Ligament Block for Ambulatory Anterior Femoral Block only Reconstruction Cruciate Ligament (ACL) Reconstruction RCT, efficacy study NCT01447277 Rec 40 Adt Jan-10 Jan-12 Vita Care http://ClinicalTrials.gov/show/NCT01358656 Comp 100 Active, NR 130 Adt Aug-08 Jan-12 Swiss National http://www.controlledSen Insurance trials.com/ISRCTN89368687 Association (SUVA) (Switzerland) Adt Dec-10 Dec-11 University of http://ClinicalTrials.gov/show/NCT00221273 Sen British Columbia Rec 50 Adt May-10 Nov-11 Glostrup Sen University Hospital, Copenhagen http://ClinicalTrials.gov/show/NCT01212666 Comp 64 Child Jul-08 Nov-11 National Police Adt Hospital http://ClinicalTrials.gov/show/NCT01513434 Monly Invite 20 Rec 225 Child Oct-09 Oct-11 Cincinnati http://ClinicalTrials.gov/show/NCT00991588 Adt Sportsmedicine Sen Research and Education Foundation Adt Oct-11 Oct-11 University of http://ClinicalTrials.gov/show/NCT01447277 Sen California, San Francisco; Joshua Cohen MD Simultaneous Multiple Cruciate Procedure: cruciate Rupture of Posterior Ligament Reconstructions Using a ligament Cruciate Ligament; Single Achilles Allograft reconstruction Rupture of Anterior Phase IV: Single group Cruciate Ligament assignment NCT01440348 Hamstrings Autograft Versus Procedure: autograft Rupture of the Tibialis Allograft for Reconstruction tendon; Procedure: Anterior Cruciate of Anterior Cruciate Ligament allograft tendon Ligament With RCT, efficacy study Instability of the NCT00510848 Knee Joint Stability of the Knee Joint After Procedure: Rupture of Anterior Single and Double Bundle Anterior 'biomechanic of the Cruciate Ligament Cruciate Ligament Reconstruction knee' RCT, efficacy study NCT01391650 Computer assisted surgery versus Arthroscopic ACL Rupture, anterior conventional arthroscopic anterior reconstruction with cruciate ligament cruciate ligament reconstruction: a computer assisted prospective randomised clinical surgery; conventional trial Arthroscopic ACL RCT (active), efficacy study reconstruction ISRCTN40231111 Clinical Trial Comparing Three Procedure: Three Knee Injuries Anterior Cruciate Ligament anterior cruciate Reconstructive Procedures ligament RCT, efficacy study reconstructive NCT00418964 procedures Evaluation of Tibial and Femoral Procedure: Anterior Anterior Cruciate Tunnel Position After Arthroscopic cruciate ligament Ligament Rupture Reconstruction of the Anterior reconstruction Cruciate Ligament Phase II: Single group assignment NCT01267435 Comp 51 Child May-11 Sep-11 National Police Adt Hospital Sen http://ClinicalTrials.gov/show/NCT01440348 Monly Adt Aug-07 Aug-11 University http://ClinicalTrials.gov/show/NCT00510848 Sen Hospital, Ghent Rec 40 Comp 60 Adt Mar-10 May-11 Hospital Znojmo; http://ClinicalTrials.gov/show/NCT01391650 Masaryk University Comp 90 Adt Dec-06 Dec-10 Erasmus Sen Medical Centre (The Netherlands) http://www.controlledtrials.com/ISRCTN40231111 Rec 42 Adt Dec-06 Nov-10 Chinese University of Hong Kong http://ClinicalTrials.gov/show/NCT00418964 Comp 40 226 Child Oct-08 Mar-10 Isfahan Adt University of Sen Medical Sciences (Iran) http://ClinicalTrials.gov/show/NCT01267435 Other Dynamic Stability of the Anterior Cruciate Ligament (ACL) Deficient Knee Non-randomised, parallel assignment, efficacy study NCT00696319 Exercise protocol Knee Injury with perturbation exercises; Exercise protocol with traditional exercises for stability and balance. Ultrasound Guided Obturator Other: Sciatic, Anterior Cruciate Nerve Block for Anterior Cruciate femoral, obturator Ligament; Surgery Ligament Reconstruction (ACL) nerve blocks; Other: RCT, safety/efficacy study Sciatic nerve block, NCT01194505 posterior lumbar plexus block BioCleanse Tibialis Tendon Other: BioCleanse Anterior Cruciate Anterior Cruciate Ligament (ACL) Tibialis tendon; Ligament Rupture Study Other: Tibialis Phase IV: RCT, efficacy study Tendon Allograft NCT00975845 from donor 65-75 years of age Changes in Muscle Morphology Other: Autograft STG Isolated Anterior Resulting From Anterior Cruciate harvest from ACL- Cruciate Ligament Ligament Reconstruction deficient leg; Other: Rupture RCT Autograft harvest NCT01537588 contralateral to ACLdeficient leg The Effect of Early Whole Body Other: Whole body Rupture of Anterior Vibration Therapy After Anterior vibration therapy; Cruciate Ligament Cruciate Ligament Reconstruction Other: Control RCT, efficacy study NCT01300182 Proprioceptive Function, Postural Other: conventional Ruptured Anterior Stability & Clinical Outcome After ACL rehabilitation Cruciate Ligament; Stump Preserving Anterior program Partial Tear Cruciate Ligament Reconstruction Ligament Surgery RCT NCT01348945 Susp 150 Child Jan-07 Jun-13 Ullevaal Adt University Hospital; University of Delaware http://ClinicalTrials.gov/show/NCT00696319 Rec 100 Adt http://ClinicalTrials.gov/show/NCT01194505 Rec 40 Adt Dec-09 Apr-13 RTI Biologics http://ClinicalTrials.gov/show/NCT00975845 Active, NR 30 Adt http://ClinicalTrials.gov/show/NCT01537588 Rec 48 Active, NR 48 227 Jun-10 May-13 Larissa University Hospital Jul-09 Jul-12 Panam Clinic Child Nov-10 Jun-12 Chinese Adt University of Sen Hong Kong; Hospital Authority Adt May-11 Feb-12 Chinese Sen University of Hong Kong http://ClinicalTrials.gov/show/NCT01300182 http://ClinicalTrials.gov/show/NCT01348945 Quadriceps Function Prior to Anterior Cruciate Ligament Reconstruction RCT, efficacy study NCT00971451 Other: cryotherapy; Other: TENS Miscellaneous observational studies Multicenter Orthopaedics Outcomes Network for ACL Reconstructions Prospective, cohort study NCT00463099 Rupture of Anterior Cruciate Ligament Rec Rupture of Anterior Cruciate Ligament Invite Multicenter Orthopaedic Outcomes Network (MOON) ACL Reconstruction (ALCR): Onsite Follow-up Prospective, cohort study NCT00478894 Rupture of Anterior Cruciate Ligament; Osteoarthritis Results of Knee Arthroscopic Surgery for Treatment of Cruciate Ligament and Meniscus Retrospective NCT01453673 Multicenter ACL Revision Study (MARS) Prospective, cohort study NCT00625885 Anterior Cruciate Ligament (ACL) Reconstruction- Bioabsorbable Screw Prospective, cohort study NCT01069588 Knee Arthroscopic Surgery 50 Child Nov-07 Dec-11 University of Adt Virginia http://ClinicalTrials.gov/show/NCT00971451 5000 Child Jan-07 Dec-16 Vanderbilt http://ClinicalTrials.gov/show/NCT00463099 Adt University; National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases Invite 400 Child Aug-07 Aug-14 Vanderbilt http://ClinicalTrials.gov/show/NCT00478894 Adt University; National Institutes of Health; National Institute of Arthritis and Musculoskeletal and Skin Diseases Active, 210 Adt May-11 May-13 Taipei Medical http://ClinicalTrials.gov/show/NCT01453673 NR Sen University WanFang Hospital Anterior Cruciate Ligament Invite 800 Child Feb-07 Nov-12 Vanderbilt Adt University ACL Reconstruction Invite 100 Child Dec-09 Feb-12 Vanderbilt http://ClinicalTrials.gov/show/NCT01069588 Adt University; Smith & Nephew, Inc. 228 http://ClinicalTrials.gov/show/NCT00625885 Follow up of Patients Operated With Anterior Cruciate Ligament Reconstruction Prospective NCT01279759 Investigation into patient characteristics and treatment factors associated with short-term and medium-term outcome following Anterior Cruciate Ligament Reconstruction ISRCTN30554985 Normal management; Measures to reduce swelling Anterior Cruciate Ligament Reconstruction Rec 35 Child Oct-10 Dec-11 Haraldsplass Adt Deaconess Sen Hospital http://ClinicalTrials.gov/show/NCT01279759 Anterior cruciate ligament reconstruction (Arthroscopic) Comp 100 Adt Apr-06 Mar-10 Department of Sen Health (UK) http://www.controlledtrials.com/ISRCTN30554985 Recruit n Age Start (Grp) Date Rec 92 Child Oct-11 Oct-14 Exactech Adt Taiwan, Ltd.; Exactech, Inc. Rec 40 Adt Rec 99 Adt Sep-10 Mar-13 The Hawkins http://ClinicalTrials.gov/show/NCT01256788 Sen Foundation; Ferring Pharmaceuticals A9E: MENISCUS/CARTILAGE PATHOLOGIES Title Phases: trial design (control) CT ID Device BiPhasic Cartilage Repair Implant (BiCRI) IDE Clinical Trial - Taiwan Phase III: RCT, safety/efficacy study NCT01477008 Interventions Conditions Device: BiPhasic Cartilage Repair Implant; Procedure: Marrow Stimulation Chondral or Osteochondral Lesion of Medial Femoral Condyle; Chondral or Osteochondral Lesion of Lateral Femoral Condyle; Chondral or Osteochondral Lesion of Trochlea Device: INSTRUCT Articular Cartilage Lesion of the Knee INSTRUCT for Repair of Knee Cartilage Defects Single group assignment, safety/efficacy study NCT01041885 Post-op Treatment With Hyaluronic Device: Euflexxa; Acid Injections Other: Saline Phase IV: RCT, efficacy study NCT01256788 Meniscus Tear; Chondropathy/Dege nerative Joint Disease (DJD) 229 End Sponsors Date URL http://ClinicalTrials.gov/show/NCT01477008 Jan-10 Mar-14 CellCoTec B.V. http://ClinicalTrials.gov/show/NCT01041885 A Prospective, Post-market, Multicenter Feasibility Study of the BioDuct® Meniscal Repair Device Single group assignment NCT01270919 ChonDux for Filling Full Thickness Cartilage Defects in the Femoral Condyle of the Knee RCT, safety/efficacy study NCT01110070 Knee Articular Cartilage Debridement in Conjunction With Partial Meniscectomy Phase IV: RCT, efficacy study NCT00613535 Device: BioDuct Meniscal Repair Device Meniscal Repair Term 35 Adt Nov-10 Jan-13 Stryker Orthopaedics http://ClinicalTrials.gov/show/NCT01270919 Device: ChonDux; Device: ChonDux Cartilage Defect Susp 60 Adt Jul-10 Jan-13 Biomet, Inc. http://ClinicalTrials.gov/show/NCT01110070 Rec 165 Adt Apr-08 Dec-12 ArthroCare Corporation http://ClinicalTrials.gov/show/NCT00613535 Not yet Rec 5 Adt Jul-11 Sep-11 Capital District http://ClinicalTrials.gov/show/NCT01290991 Health Authority, Canada Comp 80 Adt Dec-05 May-11 Piramal Healthcare Canada Ltd http://ClinicalTrials.gov/show/NCT00314236 Rec 76 Adt Aug-10 Dec-13 SK Chemicals Sen Co.,Ltd. http://ClinicalTrials.gov/show/NCT01293955 Active, NR 50 Adult Jun-08 Apr-11 Osiris Therapeutics http://ClinicalTrials.gov/show/NCT00702741 Device: Mechanical Torn Meniscus; debridement; Device: Articular Cartilage Paragon T2; Defect Procedure: Lavage debridement; Device: Mechanical Debridement; Device: RF- based Debridement Device: Augment Defect of Articular Bone Graft Cartilage A Study to Evaluate the Safety of Augment™ Bone Graft Single group assignment, safety study NCT01290991 Trial Comparing BST-CarGel and Device: BST-CarGel; Knee Injuries Microfracture in Repair of Articular Device: BST-CarGel Cartilage Lesions in the Knee RCT, safety/efficacy study NCT00314236 Drugs including biologics Assessment of Protective Effect of JOINS on Cartilage in Knee Osteoarthritis Phase IV: RCT, safety/efficacy study NCT01293955 Follow-up Study of Chondrogen® Delivered by Intra-Articular Injection Following Meniscectomy Phase I/II: RCT, safety/efficacy study NCT00702741 Drug: JOINS 200mg; Knee Osteoarthritis Drug: Placebo Drug: Chondrogen; Drug: Chondrogen; Drug: Placebo Recovery Following Partial Medial Meniscectomy 230 Autologous Transplantation of Mesenchymal Stem Cells (MSCs) and Scaffold in Full-thickness Articular Cartilage Phase I: Single group assignment, safety/efficacy study NCT00850187 Changes in Knee Articular Cartilage Volume in Women on Aromatase Inhibitors Phase IV: Cross-sectional, cohort study NCT00111241 Articular Cartilage Resurfacing With Mesenchymal Stem Cells In Osteoarthritis Of Knee Joint Phase I: Single group assignment, safety study NCT01207661 Procedure ACI-C Versus AMIC. A Randomized Trial Comparing Two Methods for Repair of Cartilage Defects in the Knee Phase II/III: RCT, efficacy study NCT01458782 Mesenchymal Stem Cells in a Clinical Trial to Heal Articular Cartilage Defects Phase I: RCT NCT00885729 Cartilage Autograft Implantation System (CAIS) for the Repair of Knee Cartilage Through Cartilage Regeneration RCT, safety/efficacy study NCT00881023 Biological: Bone marrow derived mesenchymal stem cells Knee Osteoarthritis Comp 6 Drug: aromatase Arthralgia inhibitors (letrozole, anastrozole) Active, NR 170 Biological: Mesenchymal Injection Osteoarthritis Comp Procedure: Treatment of cartilage defects in the knee Osteochondritis Dissecans; Osteoarthritis; Cartilage Injury; Osteonecrosis Procedure: stem cells; Procedure: Chondrocytes Procedure: Microfracture; Device: Cartilage Autograft Implantation System Adt Aug-08 Dec-10 Royan Institute; http://ClinicalTrials.gov/show/NCT00850187 Tehran University of Medical Sciences Adt May-05 Dec-10 Monash University Fonly http://ClinicalTrials.gov/show/NCT00111241 6 Adt Aug-09 Nov-10 Royan Institute http://ClinicalTrials.gov/show/NCT01207661 Rec 80 Adt Oct-11 Oct-24 University http://ClinicalTrials.gov/show/NCT01458782 Hospital of North Norway; University of Tromso Focal Articular Fullthickness Cartilage Defect of the Knee Rec 50 Adt Apr-09 Jul-18 Oslo University Hospital http://ClinicalTrials.gov/show/NCT00885729 Defect of Articular Cartilage; Osteochondritis Dissecans Rec 364 Adt Jul-10 Dec-16 DePuy Mitek http://ClinicalTrials.gov/show/NCT00881023 231 Efficacy and Safety Study of co.Don Chondrosphere to Treat Cartilage Defects Phase III: RCT, safety/efficacy study NCT01222559 Autologous Chondrocyte Transplantation/Implantation Versus Existing treatments RCT ISRCTN48911177 Extension Study for Patients Who Comp Previous Study MACI00206 [NCT00719576] of MACI® Implant for the Treatment of Symptomatic Articular Cartilage Defects of the Femoral Condyle Phase III: RCT, safety/efficacy study NCT01251588 Confirmatory Study of NeoCart in Knee Cartilage Repair Phase III: RCT, safety/efficacy study NCT01066702 Study for the Treatment of Knee Chondral and Osteochondral Lesions Phase IV: RCT, efficacy study NCT01282034 Knee Articular Cartilage Repair: Cartilage Autograft Implantation System Versus Conventional Microfracture Phase II: RCT NCT01498029 Procedure: Articular Cartilage Microfracture; Drug: Lesion of the co.don Femoral Condyle chondrosphere® Rec 150 Adt Oct-10 Jul-16 co.don AG http://ClinicalTrials.gov/show/NCT01222559 Autologous chondrocyte implantation (ACI); 'conventional' treatment (Debridement; Abrasion; Drilling; Microfracture; Mosaicplasty) Procedure: Microfracture; Biological: MatrixInduced Autologous Chondrocyte Implant (MACI® Implant) Symptomatic chondral defect(s) on medical or lateral femoral condyle or trochlea Active 660 N/K Dec-04 Mar-16 Keele University http://www.controlled(UK) trials.com/ISRCTN48911177/ Repair of Articular Cartilage Defects Invite 144 Adt Dec-10 May-15 Genzyme http://ClinicalTrials.gov/show/NCT01251588 Procedure: Microfracture; Biological: NeoCart Cartilage Defects of the Femoral Condyle Rec 245 Adt May-10 Mar-15 Histogenics Corporation http://ClinicalTrials.gov/show/NCT01066702 Procedure: Marrow stimulation - Drilling or Microfractures; Device: MaioRegen Surgery Procedure: Microfracture; Device: Cartilage Autograft Implantation System (CAIS) Knee Chondral Lesion; Knee Osteochondral Lesion Rec 150 Adt Jan-11 Dec-14 Fin-Ceramica Faenza Spa http://ClinicalTrials.gov/show/NCT01282034 36 Adt Jan-12 Dec-14 Singapore http://ClinicalTrials.gov/show/NCT01498029 General Hospital Other Articular Not yet Cartilage Disorders; Rec Osteochondritis Dissecans 232 Transplantation of Bone Marrow Stem Cells Stimulated by Proteins Scaffold to Heal Defects Articular Cartilage of the Knee Single group assignment, safety/efficacy study NCT01159899 Peripheral Blood-drived Stem Cell Trial on Damaged Knee Cartilage RCT NCT01076673 Evaluation of the CR Plug (Allograft) for the Treatment of a Cartilage Injury in the Knee. Phase III: Single group assignment, safety/efficacy study NCT00793104 Treatment of Cartilage Lesions in Flanders Today RCT, efficacy study NCT01421290 Assessment of Outcome of Meniscus Repair With or Without Platelet Rich Plasma Single group assignment NCT00961597 Comparison of Microfracture Treatment and CARTIPATCH® Chondrocyte Graft Treatment in Femoral Condyle Lesions Phase III: RCT, efficacy study NCT00945399 Procedure: Transplantation of Bone Marrow Stem Cells Activated in Knee Arthrosis Osteoarthritis; Knee Arthrosis; Osteochondral Defects; Osteochondritis Dissecans; Osteonecrosis Genetic: Peripheral Damaged Articular Blood derived Stem Cartilage Cell and Hyaluronic Acid; Genetic: Hyaluronic Acid Procedure: Knee Injury Placement of allograft CR Plug in primary injury site Rec 50 Adt Sen Active, NR 50 Adt Nov-09 Apr-12 Kuala Lumpur http://ClinicalTrials.gov/show/NCT01076673 Sports Medicine Centre Active, NR 20 Adt Nov-08 Mar-12 RTI Biologics Sen Procedure: Surgery; Lesion of Joint Other: Conservative Capsule of Knee comparator Region Not yet Rec 40 Adt Mar-12 Mar-12 University http://ClinicalTrials.gov/show/NCT01421290 Hospital, Ghent Procedure: Meniscus Cartilage Disease repair for red/white tears without PRP; Procedure: Meniscus repair with PRP Procedure: Knee Chondral; Microfracture; Osteochondral Procedure: Defect autologous chondrocyte implantation (CARTIPATCH® procedure) Invite 25 Rec 64 Child Sep-09 Dec-11 Cincinnati http://ClinicalTrials.gov/show/NCT00961597 Adt Sportsmedicine Sen Research and Education Foundation Adt Oct-08 Dec-11 TBF Genie http://ClinicalTrials.gov/show/NCT00945399 Tissulaire 233 Jul-10 Jun-12 University of Marseille http://ClinicalTrials.gov/show/NCT01159899 http://ClinicalTrials.gov/show/NCT00793104 Study to Compare the Efficacy and Procedure: Cartilage Injury; Safety of Cartistem® and Microfracture Osteoarthritis Microfracture in Patients With treatment; Biological: Knee Articular Cartilage Injury or Cartistem Defect Phase III: RCT, safety/efficacy study NCT01041001 RCT of ChondroCelect® (in an ACI Procedure: Articular Cartilage Procedure) vs Microfracture in the Microfracture; Drug: Lesion of the Repair of Cartilage Defects of the ChondroCelect Femoral Condyle Knee implantation Phase III: RCT, safety/efficacy study NCT00414700 Rec 104 Adt Feb-09 May-11 Medipost Co Ltd. http://ClinicalTrials.gov/show/NCT01041001 Sen Comp 118 Adt Feb-02 Jan-10 TiGenix n.v. http://ClinicalTrials.gov/show/NCT00414700 Other: DeNovo NT, Degenerative Lesion Rec Natural Tissue Graft of Articular Cartilage of Knee; Osteochondritis Dissecans Clinical Application of BioCleanse Other: BioCleanse Damaged Meniscus Active, Meniscus Meniscus NR Phase IV: Single group assignment, efficacy study NCT00659880 Novel One-step Repair of Knee Other: No PRF Meniscal Injuries Invite Meniscal Tear Using Platelet-rich Fibrin Parallel assignment NCT01211119 Resistance Exercise and Knee Other: normal Knee Osteoarthritis Rec Osteoarthritis Pain, Functional activities and clinical Impairment and Cartilage Turnover care; Other: RCT, efficacy study Concentric Focused NCT01245283 Resistance Exercise; Other: Eccentric Focused Resistance Exercise 400 Adt Feb-11 Sep-18 Zimmer Sen Orthobiologics, Inc. http://ClinicalTrials.gov/show/NCT01329445 10 Adt Apr-08 Sep-13 RTI Biologics Sen http://ClinicalTrials.gov/show/NCT00659880 18 Adt http://ClinicalTrials.gov/show/NCT01211119 90 Adt Nov-10 Nov-12 University of Sen Florida Other DeNovo NT Longitudinal Data Collection (LDC) Knee Study Cohort study NCT01329445 234 Jan-11 Dec-13 Taipei Medical University WanFang Hospital http://ClinicalTrials.gov/show/NCT01245283 Autologous Mesenchymal Stem Cells vs. Chondrocytes for the Repair of Chondral Knee Defects Phase I/II: RCT, safety/efficacy study NCT01399749 Other: Implantation of autologous cells Miscellaneous observational studies Follow-Up Trial Comparing BSTCarGel and Microfracture in Repair of Articular Cartilage Lesions in the Knee Prospective, case control study NCT01246895 Chondrocyte Maturation and Cartilage Loss Following Meniscal Injury Prospective, cohort study NCT00595803 Effects of Osteotomies Around the Knee on Cartilage Glycosaminoglycan Content Using dGEMRIC Non-invasive Imaging Prospective, cohort study NCT01269944 Articular Cartilage Lesion of the Femoral Condyle Articular Cartilage Lesions of the Knee Meniscal Tear Not yet Rec 30 Adt Sep-11 Jun-12 Fundacion para http://ClinicalTrials.gov/show/NCT01399749 la Investigacion Biomedica del Hospital Universitario la Paz Rec 80 Adt Dec-10 Mar-14 Piramal Healthcare Canada Ltd http://ClinicalTrials.gov/show/NCT01246895 Active, NR 42 Adt Aug-06 Aug-13 University of Rochester; National Institutes of Health; VirtualScopics, Inc. Adt Jul-07 Feb-11 UMC Utrecht; Sen Orthopaedics department, University Medical Center Utrecht http://ClinicalTrials.gov/show/NCT00595803 Medial Compartment Active, Osteoarthritis of the NR Knee 10 Conditions Recruit n Rec 100 http://ClinicalTrials.gov/show/NCT01269944 A9F: ARTHROPLASTY Title Interventions Phases: trial design (control) CT ID Behavioural Adding Value in Knee Arthroplasty Behavioral: Care Post-total Knee Replacement Navigator (TKR) Care Navigator Trial RCT, efficacy studyNCT01540851 Osteoarthritis; Degenerative Joint Disease 235 Age Start (Grp) Date Adt Sen End Sponsors Date Jul-11 Sep-13 Brigham and Women's Hospital URL http://ClinicalTrials.gov/show/NCT01540851 Weight Loss Intervention Before Behavioral: 8 weeks Osteoarthritis, Knee; Total Knee Replacement weight loss program, Obesity RCT, efficacy study Cambridge. NCT01469403 Guided Imagery Response in Total Behavioral: GUIDED Osteoarthritis Knee Replacement IMAGERY; Phase II: RCT, efficacy study Behavioral: NCT01491750 PLACEBO Rec 102 Rec 82 Pre-operative Rehabilitation Exercise Program for Total Knee Arthroplasty RCT, efficacy study NCT00493142 Behavioral: Exercise Osteoarthritis; Rheumatoid Arthritis Rec Comparison of Ways to Prepare Patients for Decisions About Joint Replacement Surgery Phase III: RCT NCT00911638 Behavioral: Patient decision aid and referral onward.; Behavioral: Patient education and referral onward Behavioral: Exercise Osteoarthritis; Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Active, NR Osteoarthritis, Knee Comp 38 Adt Sep-09 Dec-11 Helen Hays Sen Hospital Behavioral: Nurse dispensed oral morphine.; Behavioral: Patient self medication of oral morphine. Arthroplasty, Knee Replacement; Pain Control Rec 144 Adt Oct-10 Jun-11 The Royal http://ClinicalTrials.gov/show/NCT01226186 Sen Bournemouth Hospital; Royal Bournemouth and Christchurch Hospitals NHS Foundation Trust A Comparative Analysis of Two Types of Exercise on Outcomes Following Total Knee Arthroplasty RCT, efficacy study NCT01545986 Self Medication With Oral Morphine After Total Knee Arthroplasty. RCT, safety/efficacy study NCT01226186 Adt Aug-11 Aug-13 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT01469403 Adt Jun-11 Jan-13 Kent State http://ClinicalTrials.gov/show/NCT01491750 Sen University; National Center for Complementary and Alternative Medicine (NCCAM) 230 Adt Jul-08 Dec-12 University of http://ClinicalTrials.gov/show/NCT00493142 Sen Alberta; Alberta Heritage Foundation for Medical Research; Canadian Institutes of Health Research 340 Child May-08 Jan-12 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00911638 Adt Research Sen Institute (Canada) 236 http://ClinicalTrials.gov/show/NCT01545986 Perioperative Intervention to Improve Post-TKR Support and Function Phase II: RCT, efficacy study NCT00566826 Device A Study to Determine the Performance of the Press Fit Condylar (P.F.C.) Sigma RP-F Knee System Phase IV: Single group assignment, safety/efficacy study NCT00761410 A Prospective, Randomized Study Comparing Cemented and Cementless Total Knee Replacement RCT NCT01194817 Gender Solutions Natural Knee Post-Market Study Prospective, case-only study NCT01463566 LPS Flex Porous Femoral Components Prospective, case-only study NCT01462240 Behavioral: Patient support sessions; Behavioral: Treatment as usual Osteoarthritis; Arthroplasty, Replacement, Knee Device: P.F.C. Sigma RP-F Total Knee Replacement Osteoarthritis Rec 180 Adt Jun-08 Jun-11 National Institute http://ClinicalTrials.gov/show/NCT00566826 Sen of Arthritis and Musculoskeletal and Skin Diseases Active, NR 150 Adt Oct-04 Jan-29 DePuy Sen International Device: High-Flexion Knee Osteoarthritis Invite 100 Child Apr-10 Dec-26 Knee Replacement Adt System using Sen Cemented Fixation; Device: High-Flexion Knee Replacement System using Cementless Fixation Device: Zimmer Osteoarthritis; Not yet 300 Adt Jan-12 Jan-25 Gender(R) Inflammatory Rec Sen Solutions(TM) Arthritis; PostNatural-Knee(R) Flex traumatic Arthritis; System Rheumatoid Arthritis; Osteonecrosis; Varus or Valgus Deformities Device: LPS Flex Osteoarthritis; Not yet 300 Adt Dec-11 Dec-24 Porous Femoral Rheumatoid Arthritis; Rec Sen Components Traumatic Arthritis; Poly Arthritis; Collagen Disorders; Avascular Necrosis of Femoral Condyle; TKA 237 http://ClinicalTrials.gov/show/NCT00761410 Anderson Orthopaedic Research Institute; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01194817 Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01463566 Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01462240 A Study to Determine the Survivorship of the Press Fit Condylar (P.F.C.) Sigma Fixed Bearing Knee With a Cobalt Chrome Tibial Tray Phase IV: Single group assignment, safety/efficacy study NCT00734019 A Prospective, Clinical Investigation of the Vanguard 360 Revision Knee Phase IV: Single group assignment, safety/efficacy study NCT01542580 The Press Fit Condylar (P.F.C.) Sigma Rotating Platform (RP) TC3 Revision Knee in Revision Knee Arthroplasty Phase IV: Single group assignment, safety/efficacy study NCT00733681 Patello-Femoral Joint Post Market Clinical Follow-up Within the Knee Registry Prospective, case-only study NCT01469806 Long-Term Study of the DePuy Low Contact Stress (LCS) Complete Total Knee System Phase IV: Single group assignment, safety study NCT00733915 Sigma CR150 Versus Sigma CR Knee RCT Phase IV: RCT, efficacy study NCT01418378 Device: P.F.C. Sigma Knee Knee Osteoarthritis 700 Adt Oct-05 Oct-24 DePuy Sen International http://ClinicalTrials.gov/show/NCT00734019 Device: VANGUARD Osteoarthritis 360 Not yet 255 Rec Adt Mar-12 Apr-24 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01542580 Device: PFC Sigma Osteoarthritis RP TC3 Revision knee system Active, NR 181 Adt Mar-04 Nov-23 DePuy Sen International http://ClinicalTrials.gov/show/NCT00733681 Device: Zimmer Primary Partial Knee Not yet 120 Gender Solutions Arthroplasty; Rec PFJ Knee Prosthesis Patellofemoral Joint Adt Nov-11 Oct-23 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT01469806 250 Child Jan-02 Dec-22 DePuy Adt International Sen http://ClinicalTrials.gov/show/NCT00733915 170 http://ClinicalTrials.gov/show/NCT01418378 Device: L.C.S. Arthroplasty, Complete Knee Replacement, Knee (DePuy Low Contact Stress Complete Knee System) Device: Sigma CR150; Device: Sigma CR Osteoarthritis Active, NR Active, NR Rec 238 Adt Sen Jul-11 Sep-22 DePuy International PFC Sigma Fixed and Mobile Knee Study Phase IV: RCT, safety/efficacy study NCT00208325 Study of Knee Replacements for Patellofemoral Osteoarthritis Phase IV: RCT, safety/efficacy study NCT01326156 Signature Personalised Patient Care System With the Vanguard Knee System Study RCT NCT01092312 Device: P.F.C Sigma Osteoarthritis, Knee Fixed Bearing total knee system; Device: P.F.C Sigma RP Mobile Bearing knee system Device: Knee Osteoarthritis, Knee arthroplasty Device: Vanguard Knee System with Signature Knee Guide; Device: Vanguard Knee System with conventional Instruments Postmarketing Study for Determine Device: SIGMA HP Performance of the SIGMA HP® PARTIAL KNEE PARTIAL KNEE SYSTEM Phase IV: Single group assignment, safety study NCT01529099 Comparison of haptic assisted MAKOplasty® versus non-assisted uniunicondylar knee compartmental knee arthroplasty arthroplasty; RCT, efficacy study OXFORD® Partial ISRCTN77119437 Knee Arthroplasty Post-Market Study of the EPIK Device: EPIK™ uniKnee System compartmental knee Prospective, cohort study NCT01464632 Triathlon® PKR Outcomes Study Device: Triathlon Single group assignment PKR NCT00966979 Active, NR 684 Adt May-99 Jul-22 DePuy Sen International Rec 100 Adt Jun-07 Jun-22 University of http://ClinicalTrials.gov/show/NCT01326156 Sen Aarhus; Stryker Nordic; DePuy Orthopaedics Arthroplasty, Replacement, Knee Rec 628 Adt Mar-10 May-22 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01092312 Osteoarthritis; Posttraumatic Arthritis; Gout; Pseudo-gout Rec 200 Adt Nov-11 Apr-22 DePuy Sen International http://ClinicalTrials.gov/show/NCT01529099 Early-mid stage osteoarthritis of the knee Active 150 Adt Apr-10 Oct-21 NHS Greater Sen Glasgow and Clyde (UK) http://www.controlledtrials.com/ISRCTN77119437 Osteoarthritis; Post Traumatic Degenerative Disease Osteoarthritis; Post Traumatic Arthritis Rec 100 Adt Nov-11 Dec-20 Encore Medical, http://ClinicalTrials.gov/show/NCT01464632 L.P. Rec 184 Adt Dec-09 Dec-20 Stryker Sen Orthopaedics 239 http://ClinicalTrials.gov/show/NCT00208325 http://ClinicalTrials.gov/show/NCT00966979 A Study to Determine the Device: LCS Osteoarthritis Difference in Low Contact Stress Complete Duofix; (LCS) Duofix Versus Low Contact Device: 2 - LCS Stress (LCS) Porocoat Knee Complete Porocoat Systems Phase IV: RCT, safety/efficacy study NCT00733499 Comparing X-3 To N2vac Device: X-3 Osteoarthritis Polyethylene With the Triathlon polyethylene; Device: Total Knee System N2Vac polethylene Phase IV: RCT NCT00665964 Functional outcome of the P.F.C. P.F.C.®Sigma RP-F Osteoarthritis of the Sigma® RP-F knee system and knee system; knee the P.F.C. Sigma® knee system: A P.F.C.®Sigma knee prospective, randomised controlled system trial RCT ISRCTN64287972 Post-Market Study of the Device: 3DKnee™ Degenerative Joint 3DKnee™ System System Disease; Phase IV: Prospective, cohort Osteoarthritis; study Rheumatoid Arthritis; NCT00819481 Traumatic Arthritis A Clinical Investigation of the Device: Oxford® Osteoarthritis; Oxford® Meniscal Meniscal Avascular Necrosis Unicompartmental Knee System Unicompartmental Single group assignment Knee System NCT00578994 Prophecy Guide Outcomes in Total Device: Prophecy Osteoarthritis of the Knee Replacement Surgery Technique; Device: Knee; Total Knee Phase IV: RCT, bio-equivalence Navigation System Replacement study) NCT01163708 Total Knee Replacement Using Device: Simplex® Osteoarthritis; Simplex® or Cobalt™ Bone Bone Cement; Rheumatoid Arthritis; Cement Device: Cobalt™ Traumatic Arthritis; Prospective, cohort study Bone Cement Knee Arthritis NCT00589485 Active, NR 204 Adt Jun-07 Nov-20 DePuy Sen International http://ClinicalTrials.gov/show/NCT00733499 Wdrwn 384 Adt May-08 May-20 Dalhousie http://ClinicalTrials.gov/show/NCT00665964 Sen University; Stryker Canada LP Active 84 Adt Mar-08 Mar-19 South Tees Sen Hospitals NHS Trust (UK) Active, NR 300 Adt Feb-09 Dec-17 Encore Medical, http://ClinicalTrials.gov/show/NCT00819481 Sen L.P. Active, NR 388 Adt Mar-06 Dec-17 Biomet Sen Orthopedics, LLC Not yet 188 Rec Term 100 240 http://www.controlledtrials.com/ISRCTN64287972 http://ClinicalTrials.gov/show/NCT00578994 Adt Aug-10 Dec-17 Global http://ClinicalTrials.gov/show/NCT01163708 Sen Orthopaedic Technology; LSS Surgical Pty Ltd Adt Nov-06 Nov-17 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT00589485 Sen Lexington Clinic Oxford Partial Knee Replacement. A Randomized Clinical Trial of Three Implant Types RCT, safety/efficacy study NCT00679120 Device: Oxford Uni Osteoarthritis, Knee Knee; Device: Oxford Uni Knee; Device: Oxford Uni Knee I-beam and Cruciate Tibial Components Used in Total Knee Replacement Prospective, cohort study NCT00588783 Triathlon Total Stabilizer (TS) Outcomes Study Single group assignment NCT00958789 Prospective Multicenter Post Approval Study of the LPS-Flex Mobile Bearing Knee RCT, safety study NCT00854295 Device: I-beam design; Device: Cruciate design Clinical Outcomes and Costeffectiveness Analysis of ShapeMatch Technology Phase IV: RCT, efficacy study NCT01483066 Scorpio Cruciate Retaining (CR) Outcomes Study Single group assignment NCT00965146 Serum Metal Ion Concentration After Total Knee Arthroplasty (TKA) RCT NCT00862511 Biomechanics of Gait Pattern Adaptation in Patients After Total Knee Arthroplasty RCT NCT01412814 Device: Triathlon Total Stabilizer Rec 75 Degenerative Term Arthritis; Osteoarthritis; Rheumatoid Arthritis; Knee Arthritis Arthroplasty, Rec Replacement, Knee 100 Device: NexGen LPS-Flex Mobile Bearing Knee Osteoarthritis; Traumatic Arthritis; Avascular Necrosis of the Femoral Condyle; Moderate Varus; Valgus; Flexion Deformities Device: ShapeMatch Total Knee Technology Arthroplasty Rec 181 Adt May-09 Oct-17 University of http://ClinicalTrials.gov/show/NCT00679120 Sen Aarhus; Aarhus University Hospital; Vejle Hospital; Biomet, Inc. Adt Aug-06 Sep-17 Biomet http://ClinicalTrials.gov/show/NCT00588783 Sen Orthopedics, LLC; Lexington Clinic Adt Sen Jul-09 Jul-17 Stryker Orthopaedics 400 Child Apr-09 Dec-16 Zimmer, Inc. Adt Sen Not yet 150 Rec http://ClinicalTrials.gov/show/NCT00958789 http://ClinicalTrials.gov/show/NCT00854295 Adt Feb-12 Sep-16 Lauren Beaupre; http://ClinicalTrials.gov/show/NCT01483066 Sen Stryker Canada LP Device: Scorpio® Cruciate Retaining (CR) Total Knee System Device: Total Knee Arthroplasty (TKA) Arthroplasty, Replacement, Knee Term 228 Adt Jun-01 Jun-16 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00965146 Osteoarthritis; Metal Ion Levels Rec 120 Child Mar-09 Dec-15 Dresden Adt University of Sen Technology; Aesculap AG http://ClinicalTrials.gov/show/NCT00862511 Device: AposTherapy Biomechanical System; Other: Physical Therapy Program Knee Arthroplasty; Knee Arthritis Osteoarthritis; Osteoarthritis; Osteoarthritis, Knee; Musculoskeletal Diseases Rec 60 http://ClinicalTrials.gov/show/NCT01412814 241 Adt Sen Jul-11 Sep-15 Tel-Aviv Sourasky Medical Center A Study to Compare the Press Fit Condylar (P.F.C.) Sigma Rotatingplatform High-flexion (RP-F) Versus The Press Fit Condylar (P.F.C.) Sigma Rotating-platform (RP) Knee Implants Phase IV: RCT, safety/efficacy study NCT00733369 A Study to Evaluate the DePuy Minimally Invasive Unicompartmental Knee Phase IV: Single group assignment, safety/efficacy study NCT00734084 A Study to Evaluate the Performance of the DePuy Low Contact Stress (LCS®) Complete Anterior-Posterior Glide (APG) Mobile Bearing Knee Phase IV: Single group assignment, safety/efficacy study NCT00733486 A prospective imaging study of cruciate retaining and substituting knee replacement, in osteoarthritis and healthy aging - the PICKLeS study RCT, efficacy study ISRCTN75076749 Triathlon Posteriorly Stabilized (PS) Total Knee System Outcomes Study Non-randomized, parallel assignment NCT00957021 Device: PFC Sigma Knee Osteoarthritis RPF; Device: PFC Sigma RP Active, NR 106 Adt Nov-07 Aug-15 DePuy Sen International http://ClinicalTrials.gov/show/NCT00733369 Device: Preservation Osteoarthritis Unicompartmental Knee Active, NR 120 Adt Apr-02 Jun-15 DePuy Sen International http://ClinicalTrials.gov/show/NCT00734084 Device: L.C.S. APG Osteoarthritis Knee Anterior Posterior Glide knee Active, NR 300 Adt Aug-05 Jan-15 DePuy Sen International http://ClinicalTrials.gov/show/NCT00733486 Rotating bearing knee, retaining the posterior cruciate ligament; Posterior stabilised knee that sacrifices the posterior cruciate ligament. Device: Triathlon Posterior Stabilized (PS) Total Knee System; Device: Triathlon Posterior Stabilized (PS) Total Knee System Knee osteoarthritis, awaiting total knee replacement; Healthy agematched; Healthy Active 120 Adt Jan-12 Dec-14 Canberra Sen Hospital (Australia) http://www.controlledtrials.com/ISRCTN75076749 Arthroplasty, Replacement, Knee Active, NR 502 Adt Dec-05 Dec-14 Stryker Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00957021 242 Long-term Study of The Press Fit Device: P.F.C. Knee Osteoarthritis Condylar (P.F.C.) Sigma Total Sigma Total Knee Knee Replacement System System Phase IV: Single group assignment, safety/efficacy study NCT00734110 Multi-center, Non-comparative Device: Total Knee Noninflammatory Study of Primary Total Knee Replacement Degenerative Joint Arthroplasty (TKA) Functional Disease Performance Phase IV: Single group assignment, safety/efficacy study NCT01497730 Roentgen Stereophotogrammetric Device: Trabecular Osteoarthritis Analysis (RSA) Trial Comparing Metal Modular Tibial Trabecular Metal Monoblock and Total Knee Modular Tibial Components Component Phase IV: RCT, safety/efficacy study NCT01180595 The Fixed Bearing Lateral Fixed Bearing Lateral Osteoarthritis or Stabilised DJO 3D Knee™ versus Stabilised DJO 3D rheumatoid arthritis the Finsbury Medial Rotation Knee™; Finsbury affecting the knee Knee™ System versus the Stryker Medial Rotation Triathlon® knee in primary total Knee™ System; knee replacement for osteoarthritis Stryker Triathlon® and rheumatoid arthritis knee RCT, efficacy study ISRCTN60834248 Signature Versus Computer Device: Signature Joint Disease Assisted Surgery Study Custom Cutting Non-randomized, parallel Guides; Other: assignment Computer Assisted NCT01256216 Surgery Randomized Trial to Compare Device: Total Knee Osteoarthritis of the Axial Alignment in TKA With Use Arthroplasty Knee of Standard Instruments or Visionaire Cutting Block System. Phase III: RCT, safety/efficacy study NCT01224522 Active, NR 731 Child Oct-00 Oct-14 DePuy Adt International Sen http://ClinicalTrials.gov/show/NCT00734110 Rec 840 Adt Oct-11 Oct-14 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT01497730 Rec 50 Adt Feb-11 Sep-14 Dalhousie Sen University; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01180595 Actve 90 Adt Aug-11 Jul-14 Joint http://www.controlledSen UCL/UCLH/Roy trials.com/ISRCTN60834248 al Free Biomedical Research Unit (UK) Invite 306 Adt Sep-10 Dec-13 Biomet, Inc. Sen Rec 70 Adt Mar-11 Jul-13 Smith & Nephew http://ClinicalTrials.gov/show/NCT01224522 Sen Orthopaedics AG 243 http://ClinicalTrials.gov/show/NCT01256216 The Efficacy and Cost Analysis of Device: Hemovac Total Joint Rec Arthroplasty; Hip, Reinfusion Drains Versus drain; Device: Knee Tranexamic Acid in Total Joint OrthoPAT drain; Arthroplasty Drug: Tranexamic Phase IV: RCT, efficacy study acid NCT01514474 A Comparison Between Signature Device: Signature Arthroplasty, Rec Personalised Patient Care to Knee Guide; Device: Replacement, Knee Conventional Total Knee Conventional Arthroplasty (TKA) and Computer Instrumentation; Assisted Navigation Device: Computer RCT, safety/efficacy study Assisted Navigation NCT01145157 Roentgen Stereophotogrammetric Device: Triathlon Osteoarthritis, Knee Active, Analysis (RSA) and Dual Energy Periapatite (PA)NR X-ray Absorptiometry (DEXA) to coated Tibial Evaluate Fixation of Periapatite Component Coated Triathlon Total Knee Arthroplasty (TKA) Components Single group assignment NCT01180582 Compare the Effects of a Standard Device: Kneehab XP; Total Knee Not yet Therapy Protocol With a 12-week Device: quadriceps Replacement Rec Peri-Operative Program of TENS (at a minimal Kneehab XP Neuromuscular sensory input) using Electrical Stimulation Compared to Kneehab XP a Control Treatment in Patients Undergoing Total Knee Replacement Phase IV: RCT, efficacy study NCT01548040 Roentgen Stereophotogrammetric Device: Advance Osteoarthritis Active, Analysis (RSA) to Evaluate Biofoam porous NR Fixation of Biofoam Advance Total metal backed tibial Knee Arthroplasty Components component with or RCT, safety/efficacy study without screw NCT00657956 augmentation Long Term Foundation Knee Study Device: cruciateTotal Knee Invite Prospective, case-only study retaining Foundation Replacement NCT01274546 Knee system 234 Adt Jan-12 Jun-13 OrthoCarolina Sen Research Institute, Inc. http://ClinicalTrials.gov/show/NCT01514474 150 Adt Sen http://ClinicalTrials.gov/show/NCT01145157 30 Adt Apr-09 Apr-13 Dalhousie http://ClinicalTrials.gov/show/NCT01180582 Sen University; Stryker Orthopaedics; Capital District Health Authority, Canada 118 Adt Mar-12 Mar-13 Bio-Medical Sen Research, Ltd. http://ClinicalTrials.gov/show/NCT01548040 50 Adt Apr-08 Jan-13 Dalhousie Sen University; Wright Medical Technology http://ClinicalTrials.gov/show/NCT00657956 Jul-10 Jun-13 Biomet, Inc. 450 Child Aug-10 Jan-13 Encore Medical, http://ClinicalTrials.gov/show/NCT01274546 Adt L.P. Sen 244 Functional Performance of the Device: Total Knee Knee Arthroplasty Journey Deuce Bicompartmental Replacement; Versus the Genesis II Total Knee Device: Deuce System Phase IV: RCT, safety/efficacy study NCT01140815 Oxford Partial Knee Kinematics Device: Oxford Medial Knee Gait Analysis Study Partial Knee Compartment Single group assignment Arthritis NCT01454908 Oxford® Partial Knee Kinematics Device: Oxford® Medial Compartment Gait Analysis Study Partial Knee Arthritis Single group assignment NCT00576966 A Prospective, Randomized, Device: The Zimmer Total Knee Controlled Study Comparing Three NexGen Legacy Arthroplasty Tibial Component Designs in Total Knee System, Knee Arthoplasty modular cemented RCT, safety/efficacy study tibia; Device: The NCT00589147 Zimmer NexGen Legacy Knee System, non-modular cemented tibia.; Device: The Zimmer NexGen Legacy Knee System, nonmodular uncemented tibia Investigator Initiated Depuy PFC sigma and Knee replacement Replacement knee In-Vivo CR150 implants Evaluation Study RCT, efficacy study ISRCTN26541777 Prospective Data Collection on Device: Cementless Arthroplasty, Cementless Oxford Partial Knee Oxford Partial Knee Replacement, Knee Prospective, cohort study NCT00760188 Comparative Outcomes Device: Otto Bock C- Amputation Assessment of the C-Leg With a Leg; Device: Otto New Knee Prosthesis Bock Genium RCT, safety/efficacy study NCT01473992 Active, NR 50 Adt Sep-07 Jan-13 Anderson http://ClinicalTrials.gov/show/NCT01140815 Orthopaedic Research Institute; Smith & Nephew, Inc. Active, NR 18 Adt Apr-06 Dec-12 The CORE Sen Institute Susp 18 Adt Apr-06 Dec-12 The CORE http://ClinicalTrials.gov/show/NCT00576966 Sen Institute; Biomet, Inc. Active, NR 408 Adt Aug-03 Dec-12 Mayo Clinic; Sen Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00589147 Active 40 Adt Nov-10 Sep-12 University of Sen Leeds (UK) http://www.controlledtrials.com/ISRCTN26541777 Wdrwn 0 Adt Sen Jul-04 Sep-12 Biomet, Inc. http://ClinicalTrials.gov/show/NCT00760188 Rec 25 Adt Jan-11 Jul-12 University of South Florida; Otto Bock Healthcare; State of Florida http://ClinicalTrials.gov/show/NCT01473992 245 http://ClinicalTrials.gov/show/NCT01454908 Rehabilitation After Total Knee Device: P.F.C. Arthroplasty (TKA) - PFC Rotating Sigma knee Versus Fixed Bearing arthroplasty RCT NCT01150929 Osteoarthritis Knee Arthroplasty Performed With Device: Customized Conventional and Customized Patient Instrumentation Instrumentation; Phase IV: RCT Device: Traditional NCT01124305 Instrumentation Use of Pulsed Electromagnetic Device: Active Fields for Postoperative Knee Pain Device (Torino II); Phase II: RCT, efficacy study Device: Sham NCT01415856 Device (Torino II) Effect of TENS for Pain and Device: Placebo Function After Total Knee TENS; Device: Replacement Intense TENS (EMPI RCT, efficacy study Select TENS) NCT01364870 Impact of Noninvasive Targeted Device: Ivivi Torino Pulsed Electromagnetic Field II; Device: Ivivi (tPEMF) on Opioid Use, Pain, and Torino II Joint Function Following Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01475604 Knee Arthroplasty Registry Device: any knee Prospective, cohort study joint arthroplasty NCT01132365 device Knee Arthroplasty Uniglide™ Mobile Bearing Unicondylar Knee System vs the Uniglide™ Fixed Bearing Unicondylar Knee System Phase III: RCT, safety/efficacy study NCT00740376 Rec 50 Active, NR 52 Osteoarthritis Rec 40 Unilateral Primary Osteoarthritis of Knee; Primary Osteoarthritis of Knee Nos Osteoarthritis, Knee Rec 340 Rec 100 Osteoarthritis, Knee Invite Device: Uniglide Osteoarthritis Mobile Bearing Unicondylar Knee System; Device: Uniglide Fixed Bearing Unicondylar Knee System Rec Adt Mar-07 Jul-12 University of http://ClinicalTrials.gov/show/NCT01150929 Sen Aarhus; Regionshospital et Silkeborg; Gigtforeningen; Protesekompagniet Child May-10 Jun-12 Anderson http://ClinicalTrials.gov/show/NCT01124305 Adt Orthopaedic Sen Research Institute Adt Oct-10 May-12 Center for Joint http://ClinicalTrials.gov/show/NCT01415856 Sen Surgery and Sports Medicine, Maryland Adt May-08 May-12 University of http://ClinicalTrials.gov/show/NCT01364870 Sen Iowa Adt Nov-11 Apr-12 Amp http://ClinicalTrials.gov/show/NCT01475604 Sen Orthopedics, Inc. 3156 Adt Apr-05 Feb-12 Heekin http://ClinicalTrials.gov/show/NCT01132365 Sen Orthopedic Research Institute; DePuy Orthopaedics; Stryker Orthopaedics; ConforMIS, Inc. 420 Adt Aug-08 Feb-12 Corin http://ClinicalTrials.gov/show/NCT00740376 Sen 246 Use of Cold and Compression Therapy With Total Knee Replacement Patients Phase IV: RCT, efficacy study NCT00712816 Computer-Assisted Total Knee Arthroplasty (TKA) With Zimmer LPS Flex Knee System Phase IV: RCT NCT00300326 Optetrak Posterior Stabilized Versus Optetrak Hi-Flex Phase IV: Non-randomised, parallel assignment, efficacy study NCT00808613 Device: Game Ready Osteoarthritis; Total Injury Treatment Knee Arthroplasty System (CoolSystems Inc.); Other: Ice with compressive bandages Device: LPS Flex Total Knee knee system Arthroplasty for Knee Osteoarthritis Rec 224 Wdrwn 7 Adt Jan-06 Jan-12 Queen's Sen University; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00300326 Device: Optetrak PS; Total Knee Susp Device: Optetrak Hi- Replacement Due to Flex Osteoarthritis, Osteonecrosis, Rheumatoid; Arthritis and/or Posttraumatic Degenerative Problems Device: Standard Arthroplasty, Active, cutting guide for Replacement, Knee NR TKA; Device: Otismed MRI generated cutting guide for TKA Device: Total knee Osteoarthritis Comp arthroplasty 90 Adt Dec-08 Jan-12 Exactech Sen http://ClinicalTrials.gov/show/NCT00808613 120 Adt Jan-08 Jan-12 Department of http://ClinicalTrials.gov/show/NCT00837772 Sen Veterans Affairs 80 Adt Jan-06 Jan-12 Heekin http://ClinicalTrials.gov/show/NCT01132378 Sen Orthopedic Research Institute; Stryker Orthopaedics 35 Adt Nov-11 Dec-11 BioPoly LLC Sen Total Knee Replacement Study Using Standard Cutting Guide vs Otismed MRI Generated Cutting Guide RCT, safety/efficacy study NCT00837772 Midvastus Versus Medial Parapatellar Approach for Minimally Invasive Total Knee Arthroplasty RCT, efficacy study NCT01132378 BioPoly RS Knee Registry Study Device: BioPoly RS for Cartilage Defect Replacement Partial Resurfacing Single group assignment, Knee Implant efficacy study NCT01473199 Cartilage Injury; Defect of Articular Cartilage; Cartilage Damage Rec 247 Adt Sen Jul-08 Jan-12 CoolSystems, Inc. http://ClinicalTrials.gov/show/NCT00712816 http://ClinicalTrials.gov/show/NCT01473199 Computer-Assisted Total Knee Replacement Kinematics: DePuy Sigma Posterior Cruciate Substituting Knee and the DePuy Sigma RP Rotating Platform Knee Phase IV: RCT, efficacy study NCT00375856 Evaluation of Orthopedic Knee Measurement Using Lunar iDXA Phase I/II: Single group assignment, efficacy study NCT01348958 Comparison of High Flex and Standard Rotating Platform Total Knee Arthroplasty (TKA) RCT NCT01176292 Device: DePuy P.F.C.® Sigma Rotating Platform Knee Osteoarthritis, Knee Device: iDXA knee software Device: Rotating Platform High-Flex Cruciate Substituting TKA; Device: Rotating Platform Cruciate Substituting TKA PEAK PlasmaBlade 4.0 Versus Device: PEAK Traditional Electrosurgery in Total PlasmaBlade 4.0; Knee Replacement. Device: Traditional RCT Electrosurgery with NCT01081886 scalpel X-3 Polyethylene Survival Device: Stryker X3 Outcomes Study crosslink Phase IV: RCT, efficacy study NCT00493792 The Effectiveness of Antibiotic Device: Simplex™ P Cement (ABC) Compared to with Tobramycin; Regular Cement in Reducing the Device: Simplex™ P Rate of Infection Following Total Knee Arthroplasty: The ABC Trial Phase III: RCT, efficacy study NCT01079559 Evaluation of the Safety and Device: zirconia Effectiveness of the Kinamed Gem femoral component; Ceramic Femoral Component for Device: cobalt Total Knee Replacement chrome femoral Phase II: RCT, safety/efficacy component study NCT00743717 Rec 140 Adt Oct-06 Dec-11 Queen's Sen University; DePuy Orthopaedics http://ClinicalTrials.gov/show/NCT00375856 Hemi Knee Active, Arthroplasty; Patello- NR femoral Osteoarthritis 40 Adt May-11 Dec-11 GE Healthcare Sen http://ClinicalTrials.gov/show/NCT01348958 Knee Osteoarthritis Active, NR 142 Adt Aug-07 Dec-11 Anderson http://ClinicalTrials.gov/show/NCT01176292 Sen Orthopaedic Research Institute; DePuy Orthopaedics Degenerative Joint Disease; Osteoarthritis; Total Knee Arthroplasty Term 40 Adt Nov-09 Nov-11 Peak Surgical, Sen Inc. http://ClinicalTrials.gov/show/NCT01081886 Arthroplasty, Rec 572 Replacement, Knee; Total Knee Replacement Infection; Not yet 8800 Osteoarthritis of the Rec Knee Adt Feb-07 Sep-11 Mayo Clinic Sen http://ClinicalTrials.gov/show/NCT00493792 Knee Osteoarthritis Child Feb-04 Aug-11 Kinamed Adt Incorporated Sen Active, NR 10 248 Adt Sen Jul-10 Aug-11 University of http://ClinicalTrials.gov/show/NCT01079559 Western Ontario, Canada http://ClinicalTrials.gov/show/NCT00743717 Kneehab® pre and post total knee replacement surgery RCT ISRCTN89785408 Kneehab® group: 6 Patients undergoing weeks pre- & post- total knee knee replacement replacement surgery (30 mins of surgery. NMES twice a day for 12 weeks) + standard physiotherapy. Control group: 6 weeks pre & post surgery standard physiotherapy. Do We Need High-Flexing Total Device: legacy Osteoarthritis Knee Arthroplasty to Improve the posterior stabilized Survivorship and to Decrease the high-flexion (NexGen Incidence of Osteolysis? LPS-Flex); Device: Phase IV: RCT, efficacy study legacy posterior NCT01422642 stabilized standard (NexGen LPS) Comparison of A Mobile-Bearing Device: Sigma Knee Knee Total Knee System With A Fixed- System; Device: Bearing Total Knee System In Sigma Pressfit Cemented Total Knee Arthroplasty Condylar Posterior RCT Cruciate Substituting NCT00589108 System; Device: Sigma Pressfit Condylar Posterior Cruciate Substituting System all polyethylene tray Comparison of Total Knee Device: Zirconium Osteoarthritis Arthroplasties With Oxidized (Zirconium Genesis Zirconium and Cobalt Chromium II); Device: CobaltFemoral Components Chrome (Cobalt Phase IV: RCT, efficacy study Chrome Genesis II) NCT01336595 Long-Term Comparison of Fixed- Device: anatomic Osteoarthritis and Mobile-Bearing Total Knee modular fixedArthroplasties (TKAs) in Patients bearing; Device: low With OA ≤50 Years Old contact stress Phase IV: RCT rotating platform NCT01361152 mobile-bearing Comp 200 Adt Apr-10 Jul-11 The Royal Sen Liverpool & Broadgreen University Hospital (UK) http://www.controlledtrials.com/ISRCTN89785408 Comp 111 Adt Jan-01 Jun-11 Ewha Womans Sen University http://ClinicalTrials.gov/show/NCT01422642 Comp 240 Adt Jan-01 May-11 Mayo Clinic Sen http://ClinicalTrials.gov/show/NCT00589108 Comp 331 Adt Jan-03 Apr-11 Ewha Womans Sen University http://ClinicalTrials.gov/show/NCT01336595 Comp 216 Adt http://ClinicalTrials.gov/show/NCT01361152 249 Apr-93 Mar-11 Ewha Womans University Total Knee Arthroplasty Comparing Cementless to Cemented Fixation Phase IV: RCT, safety/efficacy study NCT01335438 A Study to Determine if Carbon Dioxide Lavage During Total Knee Surgery Reduces Intraoperative Embolic Events Phase II: RCT, efficacy study NCT00736125 Foundation Knee Study Retrospective Phase IV: Retrospective, cohort study NCT00764894 Device: Cementless Osteoarthritis (Nexgen); Device: Cemented (Nexgen) Comp 96 Adt Jan-97 Mar-11 Young Hoo Kim http://ClinicalTrials.gov/show/NCT01335438 Sen Device: pulsatile saline lavage; Device: carbon dioxide lavage Postoperative Complications; Memory Disorders Comp 40 Adt Dec-07 Mar-11 Kinamed http://ClinicalTrials.gov/show/NCT00736125 Sen Incorporated; Department of Veterans Affairs Device: Foundation Knee 200 Adt Oct-07 Feb-11 Encore Medical, http://ClinicalTrials.gov/show/NCT00764894 Sen L.P. Clinical Investigation of the LCS® Complete Posterior Stabilized Mobile-bearing Total Knee System Phase IV: Single group assignment, safety/efficacy study NCT00487565 Use of Knotless Suture for Closure of Total Hip and Knee Arthroplasties RCT, efficacy study NCT00834483 Device: Total knee arthroplasty Osteoarthritis; Post- Term traumatic Arthritis; Inflammatory Tissue Disorders; Arthritis Secondary to Other Diseases; Avascular Necrosis of the Femoral Condyles Osteoarthritis; Comp Rheumatoid Arthritis; Post-traumatic Arthritis; Juvenile Arthritis 250 Adt Sep-06 Feb-11 DePuy Sen Orthopaedics Primary Knee Active, Arthroplasty; Primary NR Hip Arthroplasty 200 Adt Feb-09 Jan-11 Rush University http://ClinicalTrials.gov/show/NCT00834483 Sen Medical Center Arthroplasty, Comp Replacement, Knee; Blood Transfusion, Autologous; Blood Transfusion 45 Adt Jan-09 Dec-10 Astra Tech AB Sen Device: Knotless suture for wound closure; Device: Layered traditional wound closure (monocryl) A Clinical Study to Investigate if Device: Bellovac Transfusion of Patients Own Shed ABT; Procedure: Blood Improves the Immunological Allogenic Blood Status in Comparison to Transfusion Transfusion of Donor Blood (“Bank Blood”")" RCT, safety/efficacy study NCT00839241 250 http://ClinicalTrials.gov/show/NCT00487565 http://ClinicalTrials.gov/show/NCT00839241 A Comparison of Fixation Method in Total Knee Arthroplasty - Low Viscosity Versus High Viscosity Bone Cement RCT, safety/efficacy study NCT00175162 NexGen Gender Fixed Bearing Knee Versus NexGen Legacy Knee Posterior Stabilized (LPS) Flex Fixed Bearing Knee: A Study Comparing Two Different Knee Prostheses RCT, safety/efficacy study NCT00901329 A Study to Compare the NexGen CR and CR-Flex Knee Implants RCT, safety/efficacy study NCT00761956 A randomised controlled trial of different knee prostheses RCT ISRCTN45837371 Device: Osteopal G Osteoarthritis vs. RefobacinPalacos R bone cement Wdrwn 50 Sen Jun-07 Dec-10 University of http://ClinicalTrials.gov/show/NCT00175162 Aarhus; Aarhus University Hospital; Biomet, Inc. Device: NexGen Total Knee Gender Fixed Arthroplasty Bearing Knee prosthesis; Device: NexGen LPS-Flex Fixed Bearing Knee prosthesis Invite 24 Adt May-07 Dec-10 Hvidovre Sen University Hospital; FZimmer, Inc. only Device: NexGen CR- Total Knee Comp 400 Adt Flex Fixed Bearing Arthroplasty; Sen Knee; Device: Osteoarthritis NexGen CR Knee Metal versus nonPrimary knee Comp 2450 Child metal backing of the replacement surgery Adt tibial component; Sen Resurface the patella; Unicompartmental versus total knee arthroplasty; Mobile versus fixed bearing Comparing Fixed-bearing Versus Device: fixed-bearing Osteoarthritis Comp 100 Child Mobile-bearing Prosthesis in Total (P.F.C.® Sigma); Adt Knee Arthroplasty: A Prospective Device: mobileSen Randomized Trial bearing (P.F.C.® Phase II: RCT Sigma) NCT01312532 The 3DKnee™ System: A PostDevice: 3DKnee Osteoarthritis; Comp 71 Adt Market Study Rheumatoid Arthritis; Sen Phase IV: Single group Post Traumatic assignment Arthritis; Varus NCT00764673 Deformity; Avascular Necrosis 251 http://ClinicalTrials.gov/show/NCT00901329 Sep-04 Dec-10 Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00761956 Dec-98 Dec-10 Department of Health (UK) http://www.controlledtrials.com/ISRCTN45837371/ Jun-04 Nov-10 Isfahan University of Medical Sciences http://ClinicalTrials.gov/show/NCT01312532 Oct-06 Oct-10 Encore Medical, http://ClinicalTrials.gov/show/NCT00764673 L.P. Prevena™ Incision Management System Over Primarily Closed Hip and Knee Incisions in Patients Immediately Post Total Hip and Knee Arthroplasty Phase IV: Single group assignment NCT01380665 Vanguard Knee Anterior Stabilized Versus Posterior Stabilized Bearing Study RCT NCT01308515 Device: Prevena Linear or Emi-linear Incisional Incisions; Total Hip Management System Arthroplasty; Total Knee Arthroplasty Device: Vanguard Osteoarthritis; Knee System with Degenerative AS Bearing; Device: Arthritis Vanguard Knee System with PS Bearing Device: mobileKnee Arthritis bearing TKA; Device: fixed- bearing TKA Comparison Between FixedVersus Mobile-bearing TKA RCT, efficacy study NCT00435357 Evaluation of Triathlon - a New Device: Triathlon Total Knee Total Knee Prosthesis System Knee System Arthroplasty Phase IV: RCT NCT00436982 Prospective Evaluation of Vitagel Device: Vitagel Arthritis for Reduction in Blood Loss and Pain Following Unilateral Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01027286 Dynamic Splinting After Total Knee Device: Knee Reduced Knee Arthroplasty Extension Dynasplint Flexion Single group assignment, efficacy study NCT00857701 Oxford Unicompartmental Knee Device: Oxford Knee Arthritis Arthroplasty With and Without Unicompartmental Navigational Unit Knee RCT, safety/efficacy study NCT00862316 Term 100 Adt Oct-09 Oct-10 KCI USA, Inc. Sen http://ClinicalTrials.gov/show/NCT01380665 Wdrwn 0 Adt Sep-10 Sep-10 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01308515 Active, NR 160 Adt Feb-07 Jul-10 Hospices Civils Sen de Lyon http://ClinicalTrials.gov/show/NCT00435357 Rec 420 Adt Dec-05 Jun-10 Stryker Nordic Sen http://ClinicalTrials.gov/show/NCT00436982 Comp 108 Adt Sen Rec 50 Adt Jan-09 May-10 Dynasplint Sen Systems, Inc. Comp 48 Child May-09 May-10 Biomet, Inc.; http://ClinicalTrials.gov/show/NCT00862316 Adt Dartmouth Sen General Hospital 252 Jul-09 Jun-10 The Cleveland http://ClinicalTrials.gov/show/NCT01027286 Clinic; Orthovita http://ClinicalTrials.gov/show/NCT00857701 Unipolar vs. Bipolar Hemostasis in Total Knee Arthroplasty: A Prospective Randomized Trial Phase IV: RCT, efficacy study NCT01003080 Device: Aquamantys Device; Other: Standard of care treatment for hemostasis during a total knee arthroplasty. A Study to Compare the NexGen Device: NexGen LPS and LPS-Flex Knee Implants LPS-Flex Fixed RCT, safety/efficacy study Bearing Knee; NCT00763386 Device: NexGen Legacy Posterior Stabilized Knee Comparing Clinical Outcome of 2 Device: Nexgen Different Total Knee Prostheses: LPS-flex and AGC Nexgen LPS-Flex Versus AGC Phase IV: RCT, efficacy study NCT00294528 Comparison of Nonposterior- and Device: PFC-Sigma Posterior-Stabilized MobileRP; Device: LPS RP Bearing Total Knee Arthroplasty Phase IV: RCT, safety/efficacy study NCT01075620 Dietary supplements Effect of Fish Oil on Surgery Pain After Knee Replacement Patients: Randomized, Prospective, Double Blind, Placebo Control Trial RCT, efficacy study NCT01274910 10% Carbohydrate Drink for Preventing Post-operative Nausea and Vomiting (PONV) After Spinal Morphine Phase I: RCT, safety/efficacy study NCT01301404 Dietary Supplement: EPAX 6000 EE 1000mg (0.6 gr DHA+EPA); Dietary Supplement: Capsules (Placebo) Dietary Supplement: 10% carbohydrate drink; Other: No intervention Knee Arthroplasty Comp 111 Adt Aug-09 Apr-10 Montefiore Sen Medical Center http://ClinicalTrials.gov/show/NCT01003080 Total Knee Arthroplasty; Osteoarthritis Comp 331 Adt Jun-01 Mar-10 Zimmer, Inc. Sen http://ClinicalTrials.gov/show/NCT00763386 Rec 100 Adt Jan-04 Jan-10 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT00294528 Comp 126 Adt May-02 Jan-10 Ewha Womans Sen University http://ClinicalTrials.gov/show/NCT01075620 Rheumatoid Arthritis Not yet Rec 60 Adt Jan-11 Mar-13 Rabin Medical Sen Center http://ClinicalTrials.gov/show/NCT01274910 Nausea and Vomiting, Postoperative; TKR 200 Adt Feb-11 Dec-12 Mahidol Sen University http://ClinicalTrials.gov/show/NCT01301404 Osteoarthritis, Knee Osteoarthritis Rec 253 Drugs including biologics Analgesic Effect of Gabapentin in Drug: Gabapentin; Total Knee Arthroplasty (TKA) Drug: Gabapentin; Phase IV: RCT, safety/efficacy Drug: Placebo study NCT01507363 Intravenous Ferric Carboxymaltose Drug: Ferinject 50 (Ferinject) in Patients Undergoing mg/ml; Drug: NaCl Orthopaedic Surgery 0.9% Phase IV: RCT, safety/efficacy study NCT01345968 Desflurane or Propofol Anesthesia Drug: propofol or in Elderly Obese Patients desflurane Undergoing Total Knee Replacement Phase IV: RCT NCT01270620 Rifampin Combination Therapy Drug: RifampinVersus Monotherapy in Early combination therapy; Staphylococcal Infections After Drug: Monotherapy Total Hip and Knee Arthroplasty Phase IV: RCT, efficacy study NCT00423982 Safety of DAbigatran and Drug: Dabigatran; RIvaroxaban Versus NAdroparin in Drug: Rivaroxaban; the Prevention of Venous Drug: Nadroparin Thromboembolism After Knee Arthroplasty Surgery Phase III: RCT, safety study NCT01431456 Clinical Trial of Gabapentin to Drug: Gabapentin Improve Postoperative Pain in Surgical Patients Phase III: RCT, safety/efficacy study NCT00221338 Analgesic Effect of Escitalopram in Drug: Escitalopram; Total Knee Arthroplasty (TKA) Drug: Placebo Phase IV: RCT, efficacy study NCT01430520 Postoperative Pain; Postoperative Sedation Rec 300 Anemia; Knee Replacement; Hip Replacement Rec 140 Obesity; Arthritis Rec 100 Prosthesis-related Infections; Staphylococcal Infections Rec 100 Child Apr-06 Dec-14 Oslo University Adt Hospital Sen Venous Thromboembolism Not yet 150 Rec Adt Jan-12 Dec-15 Hvidovre http://ClinicalTrials.gov/show/NCT01507363 Sen University Hospital; Lundbeck Foundation Adt Jun-11 Oct-15 University http://ClinicalTrials.gov/show/NCT01345968 Sen Hospital Muenster; Vifor Pharma Adt Dec-10 Dec-14 Stanford Sen University; Baxter Healthcare Corporation http://ClinicalTrials.gov/show/NCT01270620 http://ClinicalTrials.gov/show/NCT00423982 Adt Oct-11 Oct-14 Martini Hospital http://ClinicalTrials.gov/show/NCT01431456 Sen Groningen Postoperative Pain; spine, hip or knee replacement. Rec 312 Adt Aug-05 Sep-14 University of Sen California, San Francisco http://ClinicalTrials.gov/show/NCT00221338 Postoperative Pain Rec 120 Adt Sep-11 Dec-13 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT01430520 254 Duration of Leg Nerve Blocks With Drug: Pain; Total Knee Not yet 70 Dexamethasone Added to Local Dexamethasone; Arthroplasty Rec Anesthetic Drug: Ropivacaine Phase IV: RCT, efficacy study NCT01511211 Treatment of Patients Undergoing Drug: Dabigatran Arthroplasty, Rec 100 Primary Unilateral Elective Total etexilate Replacement, Knee; Knee or Hip Replacement With Venous Dabigatran Etexilate Thromboembolism Phase IV: RCT, pharmacokinetics/dynamics study NCT01184989 Daptomycin Use for Antimicrobial Drug: Daptomycin; Staphylococcal Rec 100 Prophylaxis in Methicillin Resistant Drug: Vancomycin Infections; Staphylococcus Aureus (MRSA) Methicillin-resistant Colonized Adult Patients Staphylococcus Undergoing Primary Elective Hip Aureus or Knee Arthroplasty Phase IV: RCT, efficacy study NCT01196169 Study to Observe Safety of Xarelto Drug: Rivaroxaban Prophylaxis, Not yet 500 in VTE Prophylaxis After Elective (Xarelto, BAY59Thromboembolism, Rec TKR or THR 7939) Venous; Total Knee Prospective, cohort study Replacement; Total NCT01523418 Hip Replacement Does a Single Shot Femoral Nerve Drug: Femoral Nerve Post-operative Pain; Not yet 90 Block Alone Produce Appropriate Block; Drug: TKA Rec Pain Relief? Combined nerve RCT blocks; Drug: NCT01303120 Patient-controlled analgesia Effect of Adductor-Canal-Blockade Drug: Ropivacaine; Pain After Total Rec 50 on High Pain Responders After Drug: Saline Knee Arthroplasty Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01549704 Epsilon Aminocaproic Acid Vs. Drug: Tranexamic Osteoarthritis Invite 54 Tranexamic Acid Vs. Placebo for Acid; Drug: Epsilon Prevention of Blood Loss in Total Aminocaproic Acid; Knee Arthroplasty Drug: Normal Saline RCT, safety/efficacy study NCT01527968 255 Adt Apr-12 May-13 University of Sen New Mexico http://ClinicalTrials.gov/show/NCT01511211 Adt Aug-10 Apr-13 Boehringer http://ClinicalTrials.gov/show/NCT01184989 Sen Ingelheim Pharmaceuticals Adt Oct-10 Apr-13 Mountain Home http://ClinicalTrials.gov/show/NCT01196169 Sen Research & Education Corporation; East Tennessee State University; Cubist Pharmaceuticals Adt Jun-12 Apr-13 Bayer http://ClinicalTrials.gov/show/NCT01523418 Sen Adt Mar-11 Mar-13 Hillel Yaffe Sen Medical Center http://ClinicalTrials.gov/show/NCT01303120 Adt Feb-12 Feb-13 University Sen Hospital, Gentofte, Copenhagen http://ClinicalTrials.gov/show/NCT01549704 Adt Jan-12 Jan-13 Heekin Sen Orthopedic Research Institute http://ClinicalTrials.gov/show/NCT01527968 Combination of Peripheral Nerve Block and DepoDur in Total Knee Joint Replacement Phase IV: RCT, efficacy study NCT00895531 Russian Non-Interventional Study on Compliance of Venous Thromboembolism (VTE) Prospective, case control study NCT01444586 Effectiveness of Analgesia in Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01304212 Drug: Depodur; Procedure: sciatic nerve block Arthroplasty, Replacement, Knee Rec 120 Drug: Rivaroxaban (Xarelto, BAY597939) Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Rec 2522 Adt Oct-11 Dec-12 Bayer Sen Drug: several drugs: Pain morphine chloride,ropivacaine, epinephrine,ketorola c; Drug: ropivacaine,morphin e chloride,epinephrine, ketorolac; Drug: ropivacaine; Drug: morphine ,ketorolac ChloraPrep Versus Betadine for Drug: Swab area Arthroplasty, Knee Elective Knee Replacement with Betadine; Drug: Replacement; Surgery Swab area with Replacement, Total Phase IV: RCT, bio-equivalence ChloraPrep Knee; Total Knee study Replacement NCT01184196 Local Infiltration Analgesia During Drug: The injectant Pain Total Knee Arthroplasty mixture consists of RCT, efficacy study 150 mg NCT01305733 levobupivacaine mixed with 30 mg ketorolac and 0.5 mg adrenaline; Other: saline injection Analgesia After Total Knee Drug: naropin; Drug: Total Knee Replacement Surgery marcaine; Drug: Arthroplasty RCT sufentanil; Drug: NCT01489631 neurontin Not yet 156 Rec Adt Dec-09 Dec-12 University of Sen Louisville; EKR Therapeutics, Inc Sen Apr-11 Dec-12 Consorci Sanitari de Terrassa http://ClinicalTrials.gov/show/NCT00895531 http://ClinicalTrials.gov/show/NCT01444586 http://ClinicalTrials.gov/show/NCT01304212 Rec 200 Adt Nov-09 Dec-12 Central DuPage http://ClinicalTrials.gov/show/NCT01184196 Sen Hospital Rec 70 Adt Mar-11 Dec-12 Coxa, Hospital Sen for Joint Replacement http://ClinicalTrials.gov/show/NCT01305733 Not yet Rec 60 Adt Mar-12 Nov-12 St. Antonius Sen Hospital http://ClinicalTrials.gov/show/NCT01489631 256 Xarelto for VTE Prophylaxis After Hip or Knee Arthroplasty Prospective, cohort study NCT00831714 Drug: Rivaroxaban Venous (Xarelto, BAY59Thromboembolism 7939); Drug: Standard care treatment for VTE prophylaxis Drug: warfarin; Drug: Pulmonary Fondaparinux:; Drug: Embolism warfarin Rec Prophylaxis Against DVTs After Active, Primary Hip and Knee NR Replacement Surgery RCT, safety/efficacy study NCT00767559 The Use of Evicel to Reduce Blood Drug: Evicel fibrin Patients Age 20-90; Rec Loss in Total Knee Replacement sealant Osteoarthritis Surgery Phase IV: RCT, efficacy study NCT01235715 Fibrin Sealant in Bilateral Drug: Fibrin sealant; Blood Loss Rec Simultaneous Total Knee Drug: Saline water Arthroplasty With Focus on Blood Loss, Pain, Swelling and Strength Phase IV: RCT, efficacy study NCT01472913 Platelet Rich Plasma (PRP) in Biological: Platelet Osteoarthritis; Active, Total Knee Replacement Rich Plasma Inflammatory NR Phase IV: RCT, efficacy study Arthritis NCT00826098 Can local anaesthetic injection local infiltration Undergoing total Active reduce pain in knee arthroplasty? analgesia; saline knee replacement RCT, efficacy study surgery ISRCTN35062232 Effect of Reversing Muscle Drug: Sugammadex; Neuromuscular Rec Relaxation With Sugammadex Drug: neostigmine Blockade; Compared With Usual Care on and glycopyrrolate or Arthroplasty, Bleeding Risk in Patients on Blood atropine; Drug: Replacement, Hip; Thinners Undergoing Major Joint Placebo Arthroplasty, Surgery (P07038/MK-8616-059) Replacement, Knee; Phase III: RCT, safety study Blood Coagulation; NCT01422304 Antithrombotic Agents 1500 Adt Feb-09 Nov-12 Bayer 0 Sen http://ClinicalTrials.gov/show/NCT00831714 330 Adt Nov-08 Oct-12 The New http://ClinicalTrials.gov/show/NCT00767559 Sen England Baptist Hospital 200 Adt Sep-10 Sep-12 Hospital for http://ClinicalTrials.gov/show/NCT01235715 Sen Special Surgery, New York; Ethicon, Inc. 48 Adt Aug-10 Aug-12 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01472913 170 Child Dec-08 Jun-12 Exactech Adt Sen http://ClinicalTrials.gov/show/NCT00826098 44 Adt Oct-11 May-12 University Sen Hospitals of Leicester (UK) http://www.controlledtrials.com/ISRCTN35062232 800 Adt Oct-11 May-12 Schering-Plough http://ClinicalTrials.gov/show/NCT01422304 Sen 257 Topical Tranexamic Acid and Acute Blood Loss in Total Knee Arthroplasty Phase II: RCT, safety/efficacy study NCT01370460 Effects of Pregabalin on Pain After Total Knee Arthroplasty Phase I/II: RCT, safety/efficacy study NCT01333956 Re-STOP DVT: Reload of High Dose Atorvastatin for Preventing Deep Vein Thrombosis in Statin Users Phase IV: RCT, safety/efficacy study NCT01063426 The Influence of the Femoral Nerve Block on Quadriceps Strength RCT, efficacy study NCT01111513 Drug: Tranexamic Acute Blood Loss Acid; Drug: Placebo Anemia; Osteoarthritis, Knee Rec 100 Adt Jun-11 May-12 Henry Ford Sen Health System Drug: Pregabalin 50mg; Drug: Pregabalin 100mg; Drug: Pregabalin 150mg; Drug: Placebo Drug: High dose Atorvastatin+enoxap arin; Drug: Enoxaparin Primary Total Knee Arthroplasty Rec 120 Adt May-11 Apr-12 Hospital for http://ClinicalTrials.gov/show/NCT01333956 Sen Special Surgery, New York Thrombosis; Prevention; Surgery; TKA Rec 180 Adt Nov-09 Mar-12 Hallym Sen University Medical Center http://ClinicalTrials.gov/show/NCT01063426 Total Knee Arthroplasty Rec 135 Adt Nov-07 Feb-12 Hopital de Sen l'Enfant-Jesus; Sanofi-Aventis http://ClinicalTrials.gov/show/NCT01111513 Analgesia Rec 90 Adt Mar-09 Feb-12 University of Sen Manitoba http://ClinicalTrials.gov/show/NCT00869037 Drainage Rec 600 Adt Mar-10 Dec-11 Rothman Sen Institute Orthopaedics; 3M http://ClinicalTrials.gov/show/NCT01097135 Drug: 48-hour ropivacaine infusions; Drug: Single dose ropivacaine; Drug: Patient controlled analgesics Analgesia After Total Knee Drug: Periarticular Arthroplasty Injection; Drug: Phase IV: RCT, efficacy study CFNB + Posterior NCT00869037 Capsular Injection Evaluating the Effectiveness of 2 Drug: Duraprep Surgical Skin Preparation Methods Surgical Solution in Reducing Surgical Wound Drainage After Total Hip or Knee Replacement RCT, efficacy study NCT01097135 258 http://ClinicalTrials.gov/show/NCT01370460 The Effects of Arixtra on Wound Drainage Following Total Joint Arthroplasty Phase IV: Single group assignment, safety/efficacy study NCT00909064 Effect of Oral Pregabalin on Spinal Neurotransmitters in Patients Undergoing Knee Replacement Phase III: RCT, bio-equivalence study NCT00729690 Efficacy Study of Pre-emptive Etoricoxib for Postoperative Pain and Functional Outcome in Total Knee Arthroplasty Phase II: RCT, efficacy study NCT01246362 Pradaxa (Dabigatran Etexilate) VTE Prevention After Elective Total Hip or Knee Replacement Surgery Prospective, cohort study NCT01153698 Comparison of Levobupivacaine and Ropivacaine for Femoral Neural Block Phase IV: RCT, efficacy study NCT01172197 A Comparison of Naropin and Ketorolac for Postoperative Analgesia After Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT00868348 Memantine for Post-Operative Pain Control Phase IV: RCT, safety/efficacy study NCT01041313 Drug: Fondaparinux Total Knee Sodium (Arixtra) Replacement Not yet Rec 91 Adt Jun-09 Dec-11 University of http://ClinicalTrials.gov/show/NCT00909064 Sen California, Davis Drug: Pregabalin; Drug: Pregabalin; Drug: Placebo Active, NR 48 Adt Aug-08 Dec-11 Rush University http://ClinicalTrials.gov/show/NCT00729690 Sen Medical Center PAIN Drug: Control; Drug: Knee Osteoarthritis Etoricoxib Not yet 120 Rec Adt Sen Jul-11 Nov-11 Singapore http://ClinicalTrials.gov/show/NCT01246362 General Hospital; Merck Drug: dabigatran Venous Thromboembolism; Arthroplasty, Replacement Term 167 Adt Aug-10 Nov-11 Boehringer http://ClinicalTrials.gov/show/NCT01153698 Sen Ingelheim Pharmaceuticals Drug: Levobupivacaine; Drug: Ropivacaine Pain; Arthroplasty, Replacement, Knee Susp 48 Adt Jan-09 Oct-11 NHS Tayside Sen http://ClinicalTrials.gov/show/NCT01172197 Drug: Ketorolac; Drug: NaCL Postoperative Pain Comp 60 Adt May-09 Sep-11 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT00868348 Drug: Memantine; Drug: Placebo Pain, Post-operative; THR; TKR; lumbar spinal fusion Rec 120 Adt Jan-10 Sep-11 University of Sen Washington; Forest Laboratories http://ClinicalTrials.gov/show/NCT01041313 259 Fibrin Glue or Tranexamic Acid for Total Knee Arthroplasty Phase III: RCT, safety/efficacy study NCT01306370 Drug: Tranexamic Arthropathy of Knee Rec 172 Adt Acid; Drug: Fibrin Sen glue; Biological: Fibrin glue; Other: Habitual haemostasis Local Infiltration Analgesia or Drug: ropivacaine, Osteoarthritis Rec 50 Adt Intrathecal Morphine in Total Knee ketorolac and Sen Arthroplasty epinephrine; Drug: RCT, efficacy study morphine NCT00992082 The Analgesic Efficacy of Local Drug: Total Knee Rec 42 Adt Anaesthetic Wound Infiltration Levobupivacaine; Replacement Sen Versus Intrathecal Morphine for Drug: Intrathecal Total Knee Replacement morphine Phase IV: RCT, efficacy study NCT01312415 Dose-confirmatory Bridging Study Drug: Rivaroxaban Venous Comp 302 Adt in Total Knee Replacement (BAY59-7939); Drug: Thromboembolism Sen Phase III: RCT, safety/efficacy Rivaroxaban study (BAY59-7939); Drug: NCT01206972 Rivaroxaban (BAY59-7939); Drug: Enoxaparin Optimizing Local Anesthetic Drug: 0.1% and 0.4% Total Knee Comp 48 Adt Concentration for Continuous perineural ropivicaine Arthroplasty; Knee Sen Femoral Nerve Blocks Pain Phase IV: RCT, efficacy study NCT00923598 Dabigatran Etexilate vs Drug: Dabigatran Arthroplasty, Comp 2615 Adt Enoxaparin in Prevention of Dose 1 - day 2 to Replacement, Knee; Sen Venous Thromboembolism (VTE) completion; Drug: Thromboembolism Post Total Knee Replacement Dabigatran Dose 1 Phase III: RCT, safety/efficacy day 1; Drug: study Dabigatran Dose 2 NCT00152971 day 2 to completion; Drug: Dabigatran Dose 2 - day 1; Drug: Enoxaparin 260 Jun-10 Sep-11 Fundació http://ClinicalTrials.gov/show/NCT01306370 Institut de Recerca de l'Hospital de la Santa Creu i Sant Pau Aug-09 Aug-11 University http://ClinicalTrials.gov/show/NCT00992082 Hospital Orebro Aug-10 Jun-11 Cork University http://ClinicalTrials.gov/show/NCT01312415 Hospital Oct-10 Jun-11 Bayer http://ClinicalTrials.gov/show/NCT01206972 Jun-09 Apr-11 University of http://ClinicalTrials.gov/show/NCT00923598 California, San Diego; The Cleveland Clinic Nov-04 Feb-11 Boehringer http://ClinicalTrials.gov/show/NCT00152971 Ingelheim Pharmaceuticals Morphine Consumption in Joint Replacement Patients, With or Without Gabapentin Treatment RCT, efficacy study NCT01307202 Steroids in Bilateral Total Knee Replacement Phase IV: RCT, safety/efficacy study NCT01399268 ED50 and ED95 of Intrathecal Bupivacaine With or Without Epinephrine for Total Knee Replacement Arthroplasty RCT, efficacy study NCT01264575 Drug: Gabapentin; Drug: Placebo Post Operative Pain; Comp Total Knee Replacement 101 Drug: Hydrocortisone; Drug: Saline Postoperative Inflammatory Response Comp 34 Spinal Anesthesia; Total Knee Replacement Arthroplasty Comp 162 Total Knee Arthroplasty Term 90 Drug: intrathecal bupivacaine 6mg + 100mcg OR 200mcg epinephrine; Intrathecal bupivacaine 7mg + 100mcg OR 200mcg epinephrine; Intrathecal bupivacaine 8mg + 100mcg epinephrine OR 200mcg; intrathecal bupivacaine 9mg + 100mcg epinephrine OR 200mcg; intrathecal bupivacaine 10mg + 100mcg OR 200mcg epinephrine; intrathecal bupivacaine 11mg + epinephrine 100mcg OR 200mcg The Effects of Dexamethasone on Drug: Ropivacaine; the Duration of Sciatic Nerve Drug: Blocks Dexamethasone; RCT, safety/efficacy study Drug: NCT00616603 Dexamethasone; Drug: Normal Saline 261 Adt Oct-07 Feb-11 McMaster http://ClinicalTrials.gov/show/NCT01307202 Sen University; Hamilton Health Sciences Corporation Adt Feb-09 Feb-11 Hospital for http://ClinicalTrials.gov/show/NCT01399268 Sen Special Surgery, New York; Dept. Anesthesiology, Hospital for Special Surgery Adt Dec-09 Jan-11 Seoul Medical http://ClinicalTrials.gov/show/NCT01264575 Sen Center Adt Aug-07 Jan-11 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT00616603 A Study of BIBR 1048 in Drug: Dabigatran Arthroplasty, Prevention of Venous etexilate; Drug: Replacement, Knee; Thromboembolism in Patients With Dabigatran etexilate; Venous Thrombosis TKR Surgery. Drug: Dabigatran Phase II: RCT, efficacy study Etexilate; Drug: NCT00246025 placebo RE-MODEL Dabigatran Etexilate Drug: enoxaparin; Arthroplasty, 150mg or 220mg Once Daily (o.d.) Drug: dabigatran Replacement, Knee; Versus (v.s.) Enoxaparin 40mg etexilate; Drug: Thromboembolism o.d. for Prevention of Thrombosis dabigatran etexilate After Knee Surgery Phase III: RCT, safety/efficacy study NCT00168805 Spinal Anaesthesia for Knee Drug: Lidocaine Spinal Anesthesia; Arthroscopy: Does Lignocaine added to bupivacaine Knee arthroplasty Shorten the Effect of Bupivacaine for spinal Phase IV: RCT, safety/efficacy anaesthesia study NCT01245868 Double Blind Efficacy and Safety Drug: Flexible dose Postoperative Pain Study of Flexible-Dose vs LowQ8003 (morphine Dose Q8003 After Undergoing sulfate and Primary Unilateral Total Knee oxycodone Arthroplasty hydrochloride); Drug: Phase III: RCT, safety/efficacy Low dose Q8003 study (morphine sulfate NCT01055015 and oxycodone hydrochloride) Perioperative Analgesia for Knee Femoral nerve block Elective primary Arthroplasty (PAKA) - a pilot (Levobupivicaine); unilateral total knee randomised trial Peri-articular replacement RCT infiltration ISRCTN29107680 (Levobupivacaine, Morphine + Ketorolac) Comp 512 Adt Oct-05 Jan-11 Boehringer http://ClinicalTrials.gov/show/NCT00246025 Sen Ingelheim Pharmaceuticals Comp 2101 Adt Nov-04 Jan-11 Boehringer http://ClinicalTrials.gov/show/NCT00168805 Sen Ingelheim Pharmaceuticals Comp 60 Adt Nov-09 Dec-10 Hospital of Frederikssund Comp 141 Adt Feb-10 Dec-10 QRxPharma Inc. http://ClinicalTrials.gov/show/NCT01055015 Sen Comp 46 N/K Jan-10 Dec-10 University of Warwick (UK) 262 http://ClinicalTrials.gov/show/NCT01245868 http://www.controlledtrials.com/ISRCTN29107680 Effect of Body-mass Index (BMI) Drug: BPV6NO; on Median Effective Dose of Drug: BPV7NO; Intrathecal Hyperbaric Bupivacaine Drug: BPV8NO; RCT, efficacy study Drug: BPV9NO; NCT01291186 Drug: BPV10NO; Drug: BPV11NO; Drug: BPV6O; Drug: BPV7O; Drug: BPV8O; Drug: BPV9O; Drug: BPV10O; Drug: BPV11O Postoperative Patient Controlled Drug: Epidural Analgesia After Total Levobupivacaine Knee Arthroplasty With 2ug/ml Fentanyl Combine With 0.2% Ropivacaine or 0.2% Levobupivcaine Phase IV: RCT, bio-equivalence study NCT01158586 Efficacy of Multimodal Drug: Periarticular Perioperative Analgesia With Injection - Group A; Periarticular Drug Injection in Total Drug: Periarticular Knee Arthroplasty(TKA) Injection - Group B; RCT, efficacy study Drug: Periarticular NCT01042093 Injection - Group C; Drug: Periarticular Injection - Group D Switching Drug Therapy for the Drug: Rivaroxaban Prevention of Blood Clot Formation From Enoxaparin to Rivaroxaban After Orthopedic Surgery for Either Total Hip or Total Knee Replacement Phase III: RCT, pharmacodynamics study NCT01094886 Study of Transdermal Fentanyl Drug: transdermal Patch to Treat Postoperative Pain fentanyl patch; Drug: in Total Knee Arthroplasty placebo patch Phase IV: RCT, safety/efficacy study NCT01348984 Arthroplasty, Knee Arthroplasty, Replacement, Knee; Patient-controlled Analgesia Total Knee Replacement Comp 108 Adt Jan-10 Dec-10 Seoul Medical Sen Center Rec 60 Adt Apr-10 Dec-10 United Christian http://ClinicalTrials.gov/show/NCT01158586 Sen Hospital Not yet 200 Rec Adt Jan-10 Dec-10 Towson Sen Orthopaedic Associates http://ClinicalTrials.gov/show/NCT01291186 http://ClinicalTrials.gov/show/NCT01042093 Arthritis; Comp Osteoarthritis, Knee; Osteoarthritis, Hip; Thromboembolism 56 Adt Feb-10 Dec-10 Ortho-McNeil http://ClinicalTrials.gov/show/NCT01094886 Sen Janssen Scientific Affairs, LLC Postoperative Pain 40 Adt Apr-10 Dec-10 Khon Kaen Sen University Comp 263 http://ClinicalTrials.gov/show/NCT01348984 OXN PR Compared to OXY PR in Subjects With Postoperative Pain After Knee Arthroplasty Phase IV: RCT, efficacy study NCT01083485 Pregabalin, Celecoxib, Total Knee Arthroplasty and Intrathecal Morphine Phase IV: RCT, efficacy study NCT01344213 Drug: Oxycodone/Naloxon e PR 20/10mg or 10/5mg tablets; Drug: Oxycodone Drug: Pregabalin; Drug: Celecoxib; Drug: Pregabalin with celecoxib; Drug: Placebo Post Operative Pain Comp 137 Adt Mar-10 Nov-10 Mundipharma Sen Oy Postoperative Pain Management; Total Knee Arthroplasty Comp 100 Adt Sen Local Infiltration With Bupivacaine to Increase Quality of Postoperative Pain Control in Total Knee Replacement Phase IV: RCT, efficacy study NCT01364194 A randomised controlled trial to determine if local wound infiltration reduces chronic pain after lower limb arthroplasty RCT ISRCTN96095682 Drug: 0.25% Bupivacaine; Drug: 0.9% normal saline Pain, Postoperative; Arthropathy of Knee Joint Comp 60 Comp 600 Adt Nov-09 Sep-10 Southmead Sen Hospital (UK) Rec 168 Adt May-09 Sep-10 University Health http://ClinicalTrials.gov/show/NCT00803348 Sen Network, Toronto Continuous Femoral Nerve Blockade and Readiness to Discharge Following Total Knee Arthroplasty RCT, efficacy study NCT00803348 Injection of local Hip replacement; anaesthethic into Knee replacement joint during joint replacement + standard anaesthetic; standard anaesthetic alone Drug: Bolus of 0.2% Knee Arthroplasty ropivicaine 20 mls followed by 0.2% ropivicaine at an infusion rate of 5mls/hr until 0600 on postoperative day 2; Drug: Bolus of 0.2% ropivicaine 20 mls followed by 0.1% ropivicaine at an infusion rate of 10mls/hr until 0600 on post-operative day 2; Drug: Saline control 264 http://ClinicalTrials.gov/show/NCT01083485 Jul-08 Oct-10 Chulalongkorn http://ClinicalTrials.gov/show/NCT01344213 University; Bhumibol Adulyadej Hospital; King Chulalongkorn Memorial Hospital Adt Mar-10 Sep-10 Mahidol http://ClinicalTrials.gov/show/NCT01364194 Sen University; Siriraj Hospital http://www.controlledtrials.com/ISRCTN96095682 Antibiotic Prophylaxis in Total Knee Prosthesis Phase IV: RCT, efficacy study NCT00497341 The Use of FLOSEAL to Reduce Bleeding in Total Knee Replacement Surgery Phase IV: RCT, efficacy study NCT00990288 Drug: cefuroxime; Drug: placebo Infection Drug: Hemostatic Matrix Hemorrhage Hemorrhage Risk Prescribed Arixtra Retrospective, cohort study NCT01064362 Drug: Fondaparinux sodium; Drug: Low molecular weight heparin (LMWH) Prospective, Randomized Controlled Trial on Perioperative Pregabalin to Reduce Late-onset CRPS After TKA Phase II: RCT, efficacy study NCT00558753 Clinical Trial for Fibrin Sealant in Knee Surgery RCT, efficacy study NCT00440921 Additional Anti-emetic Effect of Ramosetron Prophylaxis After Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01102491 Single Intravenous Administration of TB-402 for the Prophylaxis of Venous Thromboembolic Events (VTE) After Total Knee Replacement Surgery Phase II: RCT, safety/efficacy study NCT00793234 Drug: pregabalin; Drug: Placebo Knee Replacement Surgery; Haemorrhage; Thrombosis, Venous; Hip Replacement Surgery; Hip Fracture Surgery Complex Regional Pain Syndromes Drug: Single donor Allogenous Fibrin Sealant Drug: Ramosetron Rec 1332 Adt Jan-08 Aug-10 Hospital Clinic of http://ClinicalTrials.gov/show/NCT00497341 Sen Barcelona 196 Child Oct-07 Aug-10 Hospital for http://ClinicalTrials.gov/show/NCT00990288 Adt Special Surgery, Sen New York; Baxter Healthcare Corporation Comp 1344 Adt Jan-10 Jun-10 GlaxoSmithKline http://ClinicalTrials.gov/show/NCT01064362 2 Sen Comp 240 Adt Apr-06 Jun-10 Rush University http://ClinicalTrials.gov/show/NCT00558753 Sen Medical Center; Pfizer Total Kneereplacement; Total Hip-replacement Wdrwn 578 Osteoarthritis, Knee Comp 153 Adt Dec-08 Jun-10 Sanquin http://ClinicalTrials.gov/show/NCT00440921 Sen Research & Blood Bank Divisions; MDM Adt Sep-09 Mar-10 Seoul National http://ClinicalTrials.gov/show/NCT01102491 Sen University Hospital Comp 316 Drug: TB-402; Drug: Total Knee Enoxaparin Replacement Surgery Comp 265 Adt Dec-08 Mar-10 ThromboGenics; http://ClinicalTrials.gov/show/NCT00793234 Sen BioInvent International AB; Covance A Phase 3 Study of DU-176b, Prevention of Venous Thromboembolism in Patients After Total Knee Arthroplasty Phase III: RCT, safety/efficacy study NCT01181102 Safety and Efficacy Study of KAI1678 to Treat Subjects With Postoperative Pain Phase II: RCT, safety/efficacy study NCT01015235 Procedure Long-Term Multicenter Evaluation of the E1® Tibial Bearing Single group assignment NCT01374230 Computer Navigation vs Conventional Technique in Knee Arthroplasty RCT, efficacy study NCT00782444 Posterior cruciate ligament and total knee arthroplasty: retain, sacrifice or substitute? A prospective, randomised clinical trial RCT, efficacy study ISRCTN82612978 Hospital for Special Surgery Knee Arthroplasty Cohort Prospective, cohort study NCT00454467 Drug: edoxaban; Drug: enoxaparin sodium Prevention; Venous Thromboembolism Comp 716 Adt Mar-09 Feb-10 Daiichi Sankyo http://ClinicalTrials.gov/show/NCT01181102 Sen Inc.; Daiichi Sankyo, Tokyo, LTD. Drug: Placebo; Drug: Pain, Postoperative; THR; TKR KAI-1678; Drug: Ketorolac Tromethamine Comp 90 Adt Dec-08 Feb-10 KAI http://ClinicalTrials.gov/show/NCT01015235 Sen Pharmaceuticals ; Trident Clinical Research Pty Ltd Procedure: Total knee arthroplasty Not yet Rec 50 Adt Sep-11 Sep-21 Massachusetts http://ClinicalTrials.gov/show/NCT01374230 Sen General Hospital Procedure: computer Knee Osteoarthritis; Active, navigation Rheumatoid Arthritis NR 200 Total Knee Arthroplasty (TKA) with Posterior Cruciate Ligament (PCL) retained; TKA with PCL excised, but not replaced; TKA with PCL excised and replaced with posterior stabilised implant 285 Adt Jan-09 Dec-18 Haukeland http://ClinicalTrials.gov/show/NCT00782444 Sen University Hospital; The Research Council of Norway Adt Apr-06 Dec-18 Helsinki http://www.controlledSen University trials.com/ISRCTN82612978 Central Hospital (Finland) Osteoarthritis of the Knee; Traumatic Arthritis of the Knee Severe Knee Osteoarthritis Knee Arthroplasty Active Rec 3000 Adt Apr-07 Apr-17 Hospital for http://ClinicalTrials.gov/show/NCT00454467 Sen Special Surgery, New York; Agency for Healthcare Research and Quality (AHRQ) 266 Total or Partial Knee Arthroplasty Trial RCT, efficacy study NCT01352247 Procedure: Unicompartmental Knee Replacement; Procedure: Total Knee Replacement Articulating Versus Static Antibiotic Procedure: Static Loaded Spacers for the Treatment Spacer; Procedure: of Prosthetic Knee Infection Articulating Spacer RCT, efficacy study NCT01373112 Outcomes After Total Knee Joint Arthroplasty : A Comparative Study Using 3 Different Analgesic Techniques Phase III: RCT, safety/efficacy study NCT01503528 Motion Analysis of EMP Knee Versus Posterior Stabilized Knee Arthroplasty for Osteoarthritis RCT NCT00967161 Clinical and Stereoradiological Comparison of the Results After Primary Cemented Total Knee Arthroplasty Inserted With or Without the Use of a Tourniquet Phase IV: RCT, efficacy study NCT01488175 Total Knee Arthroplasty (TKA) Cemented Versus Cementless Tibial Prosthesis Study Phase II/III: RCT, efficacy study NCT01041937 Knee Osteoarthritis Rec 500 Adt Jan-10 Dec-16 University of Sen Oxford; University of Aberdeen http://ClinicalTrials.gov/show/NCT01352247 Osteoarthritis; Knee Rec 140 Infection; Prosthetic Joint Infection; Complications; Arthroplasty, Infection or Inflammation; Complications; Arthroplasty Knee Joint Arthritis; Not yet 750 Knee Joint Rec Arthroplasty Adt Dec-11 Aug-16 Rush University http://ClinicalTrials.gov/show/NCT01373112 Sen Medical Center; Central DuPage Hospital 50 Adt Jan-12 Jun-15 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00967161 Sen Research Institute; Wright Medical Technology Adt Jan-12 Jan-15 Hvidovre http://ClinicalTrials.gov/show/NCT01488175 Sen University Hospital Procedure: Spinal anesthesia with periarticular infiltration; Procedure: Femoral and sciatic nerve blocks; Procedure: Periarticular infusions Procedure: Total Arthropathy of Knee Not yet Knee Arthroplasty; Joint Rec Procedure: Motion analysis Procedure: tourniquet; Procedure: no tourniquet Osteoarthritis of the Knee Not yet Rec 60 Procedure: Cemented Tibia; Procedure: Cementless Tibia Osteoarthritis; Post- Active, traumatic NR Osteoarthritis; Rheumatoid Arthritis 250 267 Adt Jun-12 Aug-15 Lawson Health Sen Research Institute http://ClinicalTrials.gov/show/NCT01503528 Adt Dec-09 Dec-14 Washington http://ClinicalTrials.gov/show/NCT01041937 Sen University School of Medicine; Wright Medical Technology Comparison of Three Tourniquet Application Methods in Primary Total Knee Arthroplasty Surgery RCT NCT01355900 Application of Radiostereometric Analysis (RSA) to Triathlon Knee Components Inserted Using the OtisMed Custom-fit Total Knee Replacement System RCT, efficacy study NCT01262430 Effect of Preop Nutritional Status on Outcomes of Staged Bilateral Total Knee Arthroplasty Prospective, cohort study NCT01545362 Patellar Resurfacing in Total Knee Arthroplasty RCT, efficacy study NCT00553982 Adductor-Canal-Blockade Versus the Femoral Nerve Block Effect on Muscle Strength, Pain and Mobilization After Total Knee Replacement RCT, efficacy study NCT01470391 Total Knee Arthroplasty Accelerated Recovery Without Tourniquet RCT NCT01309035 Dilute Betadine Lavage in the Prevention of Postoperative Infection Phase IV: RCT, efficacy study NCT01175044 Procedure: Total knee arthroplasty performed under tourniquet Knee Osteoarthritis Procedure: OtisMed; Osteoarthritis Procedure: Computer Assisted Surgery (CAS) Procedure: Total knee arthroplasty Arthritis Procedure: Patellar Osteoarthritis; Pain component; Procedure: No patellar component Procedure: Adductor- Total Knee Canal-Blockade; Arthroplasty Procedure: Femoral Nerve Block Procedure: Total Knee Arthroplasty Osteoarthrosis in Knee-joint Procedure: Betadine Prosthesis-Related Lavage; Procedure: Infections; Arthroplasty; TKA Saline Lavage Rec 120 Adt Jan-10 Dec-14 Vilnius Sen University; Karolinska Institutet http://ClinicalTrials.gov/show/NCT01355900 Rec 50 Adt Apr-11 Apr-14 Dalhousie Sen University http://ClinicalTrials.gov/show/NCT01262430 Invite 100 Adt Nov-11 Mar-14 Heekin Sen Orthopedic Research Institute http://ClinicalTrials.gov/show/NCT01545362 Active, NR 110 Child Oct-07 Dec-13 Sykehuset Adt Innlandet HF Sen http://ClinicalTrials.gov/show/NCT00553982 Rec 55 Adt Nov-11 Sep-13 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01470391 Rec 60 Adt Mar-11 Sep-13 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT01309035 Rec 600 Adt Aug-10 Aug-13 Rush University http://ClinicalTrials.gov/show/NCT01175044 Sen Medical Center; Central DuPage Hospital 268 Efficacy and Patient Satisfaction With AQUACEL® Ag Surgical Dressing Compared to Standard Surgical Dressing RCT, safety/efficacy study NCT01258270 Total knee arthroplasty versus patellofemoral arthroplasty in patients with severe arthritis of the patellofemoral joint RCT ISRCTN34863373 Minimally Invasive Knee Replacement Outcomes (MIKRO) Study RCT, efficacy study NCT00633113 Anatomic Reconstruction of the Patellofemoral Joint Phase IV: RCT, efficacy study NCT01375231 Procedure: Postop Wound Healing; Dressing; Procedure: TKA; THA Postop Dressing Rec 300 Adt Dec-10 Aug-13 OrthoCarolina Sen Research Institute, Inc.; ConvaTec Inc. http://ClinicalTrials.gov/show/NCT01258270 http://www.controlledtrials.com/ISRCTN34863373 Total knee arthroplasty; Patellofemoral arthroplasty Patellofemoral osteoarthritis Active 64 Adt Mar-09 Apr-13 University of Sen Warwick (UK) Procedure: MPPA; Procedure: SV Knee Osteoarthritis Active, NR 128 Adt Nov-07 Mar-13 Dartmouthhttp://ClinicalTrials.gov/show/NCT00633113 Sen Hitchcock Medical Center; Zimmer, Inc. Procedure: Knee Replacement Active, 52 Child Jun-11 Jan-13 OrthoCarolina Measured Resection Surgery NR Adt Research of patellofemoral Sen Institute, Inc. joint; Procedure: Measured resection of patella Minimally Invasive Versus Procedure: Osteoarthritis; Rec 50 Child Nov-07 Jan-13 Aesculap AG Conventional Approaches in Navigated TKA with Rheumatoid Arthritis; Adt Navigated Total Knee Arthroplasty a minimally invasive Post-traumatic Sen (TKA) approach; Arthritis Phase IV: RCT, efficacy study Procedure: NCT00839020 Navigated TKA with a conventional approach MR Imaging of Knee Osteoarthritis Procedure: ACL Osteoarthritis, Knee Active, 145 Adt Aug-06 Dec-12 University of and Acute Knee Injuries Reconstruction NR Sen California, San Prospective, case control study Surgery; Procedure: Francisco; NCT00504114 Cartilage National Resurfacing Surgery; Institutes of Procedure: Total Health Knee Replacement Saphenous Nerve Block vs. Procedure: Study Difference Between Not yet 60 Adt Feb-12 Nov-12 Hospital for Femoral Nerve Block for Total Technique; Femoral Nerve Block Rec Sen Special Surgery, Knee Arthroplasty Procedure: Control and Saphenous New York RCT, safety/efficacy study Technique Block NCT01505374 269 http://ClinicalTrials.gov/show/NCT01375231 http://ClinicalTrials.gov/show/NCT00839020 http://ClinicalTrials.gov/show/NCT00504114 http://ClinicalTrials.gov/show/NCT01505374 Perioperative Analgesia After Knee Procedure: Knee Arthroplasty Arthroplasty Continuous femoral Phase IV: RCT, efficacy study nerve block + NCT01225484 periarticular infiltration; Procedure: Intraarticular and periarticular ropivacaine A Randomized Controlled Trial of Procedure: Waiting Osteoarthritis Long Versus Short Wait For time (access time to Primary Total Hip and Knee Total joint Arthroplasty replacement) Phase IV: RCT, efficacy study NCT00138892 Early Ambulation After Adductor Procedure: Canal Pain; Osteoarthritis Canal Block for Total Knee Block and Capsular Arthroplasty Injection; Procedure: RCT, efficacy study Femoral Nerve Block NCT01459861 with Tibial Nerve Block Osteoarthritis; TKA; Study Comparing Peri-articular Procedure: PeriInjection of Bupivacaine With and articular injection of THA Without Epinephrine marcaine/epinephrin RCT, efficacy study e; Procedure: PeriNCT00737139 articular injection of marcaine alone Effect of Prophylactic Antibiotics Procedure: Infection; Arthroplasty; Hip; on Intra-Operative Culture Results Prophylactic Knee Phase IV: RCT, efficacy study Antibiotics; NCT01174212 Procedure: Control Antibiotics Effect of a Sciatic Nerve Block Procedure: Postoperative Pain Combined With a Continuous Analgesia for knee Femoral Block on Pain Scores arthroplasty After Knee Arthroplasty RCT, efficacy study NCT01337115 Preoperative Alignment of Total Procedure: Knee Arthritis Knee Replacement customized knee RCT, efficacy study instruments; NCT01242085 Procedure: total knee replacement Rec 123 Adt Oct-10 Oct-12 Landeskrankenh http://ClinicalTrials.gov/show/NCT01225484 Sen aus Feldbach; Medical University of Graz Active, NR 236 Adt Aug-02 Oct-12 University of http://ClinicalTrials.gov/show/NCT00138892 Sen British Columbia Rec 56 Adt Oct-11 Sep-12 Saint Francis Sen Care Rec 240 Adt Sep-08 Sep-12 Rush University http://ClinicalTrials.gov/show/NCT00737139 Sen Medical Center Rec 200 Adt Sen Active, NR 50 Rec 60 270 http://ClinicalTrials.gov/show/NCT01459861 Jul-10 Jul-12 Rush University http://ClinicalTrials.gov/show/NCT01174212 Medical Center; Rothman Institute Orthopaedics Child Apr-11 Jun-12 Centro http://ClinicalTrials.gov/show/NCT01337115 Adt Hospitalar do Sen Porto; Universidade do Porto Adt Nov-10 Jun-12 VA Palo Alto http://ClinicalTrials.gov/show/NCT01242085 Sen Health Care System; DePuy Orthopaedics Effectiveness of Minimally Invasive Procedure: Minimally Osteoarthritis Total Knee Replacement in Invasive Total Knee Improving Rehabilitation and Arthroplasty Function [TKA(min)]; Phase II: RCT, efficacy study Procedure: Total NCT00710840 Knee Arthroplasty (TKA) Standard Total Knee Arthroplasty Procedure: Total Osteoarthritis Using Platelet Rich Plasma (PRP) knee arthroplasty RCT, efficacy study NCT01075230 Intraoperative Posterior Cruciate Procedure: Arthroplasty, Ligament (Transcruciate) Injection transcruciate Replacement, Knee After Total Knee Arthroplasty injection of 20cc of (TKA) normal saline; Phase IV: RCT, efficacy study Procedure: NCT01345604 transcruciate injection of 20 cc of 0.5% Ropivacaine New Tool of Subjective and Procedure: Hip Arthritis; Knee Objective Functional Evaluation Arthroplasty Arthritis and the Quality of Life After Arthroplastic Surgery of the Hip and the Knee Assisted or Not by Computer and Mini-invasive Arthroplasty RCT NCT00894218 Effectiveness of Acupuncture as Procedure: Total Knee an Adjunct to Rehabilitation After Acupuncture; Replacement Knee Arthroplasty Procedure: exercises RCT, safety/efficacy study NCT00935155 Review on Minimally Invasive Skin Procedure: Incision Gonarthrosis Incision in Vanguard PS Artificial technique; Patients Who Need Knee Joint System Procedure: Incision Artificial Knee Joint RCT, safety/efficacy study technique Total Replacement NCT01010828 Active, NR 75 Adt Jun-08 Jun-12 Greg Olender; http://ClinicalTrials.gov/show/NCT00710840 Sen National Institute of Arthritis and Musculoskeletal and Skin Diseases Active, NR 100 Child Feb-10 Jun-12 Exactech Adt Sen http://ClinicalTrials.gov/show/NCT01075230 Invite 40 Child May-11 May-12 University of http://ClinicalTrials.gov/show/NCT01345604 Adt Saskatchewan; Sen Saskatoon Health Region Rec 80 Adt Apr-09 Apr-12 Assistance Sen Publique Hopitaux De Marseille http://ClinicalTrials.gov/show/NCT00894218 Rec 170 Adt Jan-09 Mar-12 Back and Sen Rehabilitation Center, Copenhagen http://ClinicalTrials.gov/show/NCT00935155 Rec 72 Child Nov-09 Mar-12 Biomet, Inc.; Adt Biomet Japan, Sen Inc. http://ClinicalTrials.gov/show/NCT01010828 271 The Efficacy of Adductor-CanalBlockade on Pain and Morphine Consumption After Revision Knee Arthroplasty Phase IV: RCT NCT01191593 The Effect of Ischemic Preconditioning on Postoperative Pain After Total Knee Arthroplasty, a Randomized, Controlled Trial RCT, safety/efficacy study NCT01333969 Continuous Saphenous Nerve Block for Total Knee Arthroplasty RCT, efficacy study NCT01332045 Procedure: Adductor- Postoperative Pain; Canal-Blockade with Knee Arthroplasty Ropivacaine; Procedure: AdductorCanal-blockade with saline Procedure: Ischemic Total Knee Preconditioning Arthroplasty; Ischemic Preconditioning; Postoperative Pain Procedure: Pain, Postoperative continuous saphenous nerve block; Procedure: Saline boluses in nerve catheter General vs. Intrathecal Anesthesia Procedure: General Arthritis for Total Knee Arthroplasty anesthesia; RCT Procedure: Regional NCT01312298 anesthesia Anterior Referencing Versus Procedure: Total Osteoarthritis Posterior Referencing in Minimally knee Invasive Total Knee Arthroplasty RCT, efficacy study NCT01135030 Continuous Saphenous Block Procedure: Total Knee Versus Continuous Femoral Block continuous femoral Arthroplasty for Total Knee Arthroplasty nerve block; Secondary to RCT Procedure: Osteoarthritis NCT01250041 continuous saphenous nerve block Do We Need Computer Assistance Procedure: NonOsteoarthritis To Improve the Survival of Primary Computer Assistance Total Knee Arthroplasty. A TKA; Procedure: Minimum Ten Years Follow-up Computer Assistance Phase IV: RCT TKA NCT01520571 Rec 36 Adt Sep-10 Feb-12 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01191593 Rec 60 Comp 40 Adt Apr-11 Feb-12 Hospital for http://ClinicalTrials.gov/show/NCT01333969 Sen Special Surgery, New York; University of Massachusetts, Worcester Adt Apr-11 Jan-12 Henning Lykke http://ClinicalTrials.gov/show/NCT01332045 Sen Andersen Not yet 120 Rec Adt Aug-11 Jan-12 Region Skane Sen Comp 100 Not yet Rec 40 Adt Oct-06 Jan-12 Heekin http://ClinicalTrials.gov/show/NCT01135030 Sen Orthopedic Research Institute; Stryker Orthopaedics Adt Jan-11 Dec-11 McGill University http://ClinicalTrials.gov/show/NCT01250041 Sen Health Center Comp 520 272 Adt Jan-00 Dec-11 Ewha Womans Sen University http://ClinicalTrials.gov/show/NCT01312298 http://ClinicalTrials.gov/show/NCT01520571 Early Neuromuscular Electrical Procedure: Osteoarthritis Stimulation For Quadriceps Muscle Neuromuscular Activation Deficits Following Total Electrical Stimulation Knee Replacement (NMES); Behavioral: Phase II: RCT, efficacy study Standard NCT00800254 Rehabilitation Protocol Comp 66 Comparing Postoperative Procedure: Sciatic Total Knee Rec 96 Functional Recovery and Nerve Block; Arthroplasty; Post Analgesic Efficacy of a Single Shot Procedure: Posterior Operative Analgesia Sciatic Nerve Block Versus capsule infiltration Posterior Capsule/Fat Pad with local anesthetic; Infiltration of Local Anesthetic for Procedure: Sham Total Knee Arthroplasty sciatic block and RCT, efficacy study sham posterior NCT00677261 infiltration Saphenous Nerve Block Versus Procedure: Study Total Knee Comp 73 Femoral Nerve Block for Total Group: Experimental; Arthroplasty Knee Arthroplasty Procedure: Control Phase IV: RCT, safety/efficacy Group study NCT01333943 An Efficacy and Safety Study of Procedure: parecoxib Unilateral Primary Not yet 125 Periarticular Parecoxib Sodium for sodium; Procedure: Osteoarthritis of Rec Pain Management in Total Knee parecoxib sodium Knee Arthroplasty Phase III: RCT, safety/efficacy study NCT01311804 Accuracy of MRI-based Patients Procedure: Patient Osteoarthritis of Comp 80 Matched Instruments vs Jig-based matched Knee Instruments in Total Knee instruments; Arthroplasty (TKA) Procedure: Jig based RCT, efficacy study instruments NCT01449474 273 Adt Oct-08 Nov-11 Greg Olender; http://ClinicalTrials.gov/show/NCT00800254 Sen National Institute on Aging (NIA); University of Colorado, Denver; American College of Rheumatology Research and Education Foundation Adt Jun-08 Nov-11 Sunnybrook http://ClinicalTrials.gov/show/NCT00677261 Sen Health Sciences Centre Adt Mar-11 Nov-11 Hospital for http://ClinicalTrials.gov/show/NCT01333943 Sen Special Surgery, New York Adt Apr-11 Oct-11 Ministry of http://ClinicalTrials.gov/show/NCT01311804 Sen Health, Malaysia Adt Apr-11 Oct-11 Mahidol Sen University http://ClinicalTrials.gov/show/NCT01449474 Prediction of Pain in Total Knee Arthroplasty Single group assignment NCT01179204 The Recovery Time of Quadriceps Strength After Total Knee Arthroplasty (TKA): The Effect of Quadriceps Incision Length RCT, efficacy study NCT01450904 The Efficacy of Adductor-CanalBlockade on Pain and Morphine Consumption After Total Knee Arthroplasty Phase IV: RCT, efficacy study NCT01261897 Minimal Versus Conventional Exposure in Unicompartmental Knee Arthroplasty RCT, efficacy study NCT00991445 Minimally Invasive Surgical Approaches In Total Knee Arthroplasty RCT, efficacy study NCT01461356 Navigated EM Total Knee Replacement: Accuracy Study Prospective, cohort study NCT00512421 Analgesia After Total Knee Arthroplasty: Peri-Articular Injection Versus Epidural + Femoral Nerve Blockade Phase IV: RCT, efficacy study NCT01335542 Patellofemoral Pain After Unicondylar Knee Arthroplasty Prospective, case-only study NCT01407042 Procedure: Preoperative heat stimulation Pain, Postoperative Comp 100 Adt Aug-10 Oct-11 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01179204 Procedure: Osteoarthritis of Quadriceps incision Knee < 2 cm; Procedure: Quadriceps incision 2-4 cm; Procedure: Quadriceps incision > 4 cm Procedure: Adductor- Postoperative Pain; Canal-Blockade with Knee Arthroplasty Ropivacaine; Procedure: AdductorCanal-blockade with saline Procedure: Minimal Knee Osteoarthritis Invasive Surgery; Procedure: Conventional exposure Procedure: Minimally Knee Osteoarthritis invasive total knee replacement; Procedure: Standard approach total knee replacement Procedure: Total Knee computer-assisted Replacement surgery Comp 60 Adt Apr-11 Oct-11 Mahidol Sen University http://ClinicalTrials.gov/show/NCT01450904 Comp 40 Adt Jan-11 Sep-11 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01261897 Rec 40 Adt May-09 Sep-11 University http://ClinicalTrials.gov/show/NCT00991445 Sen Hospital Orebro Comp 40 Adt Mar-07 Sep-11 Mayo Clinic Sen Term 200 Adt Sen Rec 90 Adt Mar-10 Aug-11 Hospital for http://ClinicalTrials.gov/show/NCT01335542 Sen Special Surgery, New York Not yet Rec 20 Adt Sep-11 Jul-11 Medical Sen University Innsbruck Procedure: PeriReadiness to Articular Injection; Discharge Procedure: Epidural Pathway (PCEA+FNB) Procedure: mobile- Mobile-bearing bearing unicondylar Unicondylar Knee knee arthroplasty Arthroplasty 274 Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT01461356 http://ClinicalTrials.gov/show/NCT00512421 http://ClinicalTrials.gov/show/NCT01407042 Rec 400 Adt Nov-07 Jul-11 Minneapolis http://ClinicalTrials.gov/show/NCT00979147 Sen Veterans Affairs Medical Center (VAMC); Depuy, Inc. Wdrwn 90 Procedure: Adductor- Total Knee Canal-Blockade; Arthroplasty Procedure: AdductorCanal-blockade with saline Comp 70 Adt Mar-07 Jun-11 HealthEast Care http://ClinicalTrials.gov/show/NCT00455182 Sen System; University of Minnesota Clinical and Translational Science Institute; Northwestern Health Sciences University Adt Aug-10 Mar-11 Rigshospitalet, http://ClinicalTrials.gov/show/NCT01104883 Sen Denmark Procedure: Surgical Osteoarthritis approach for total knee arthroplasty Comp 126 Child Jan-05 Mar-11 Capital District http://ClinicalTrials.gov/show/NCT00346788 Adt Health Authority, Sen Canada Procedure: Total Osteoarthritis of the Knee Arthroplasty Knee with Custom Cutting Blocks; Procedure: Total Knee Arthroplasty via Computer Assisted Surgery Comp 60 Comparison of a Metal Backed Procedure: TKA Osteoarthritis, Knee Fixed-Bearing Tibial Baseplate and surgery with modular an All-Polyethylene Tibia in Total polished tibial Knee Arthroplasty baseplate/XLK Phase IV: RCT, safety/efficacy design; Procedure: study TKA surgery with the NCT00979147 nonmodular APT/GVF design; Device: P.F.C.® Sigma Knee System; Device: P.F.C.® Sigma Knee System Acupuncture for Pain Management Procedure: Pain; Postoperative After Hip or Knee Arthroplasty Acupuncture; Complications RCT, efficacy study Procedure: Sham NCT00455182 Acupuncture; Procedure: Standard medical care The Efficacy of Adductor-CanalBlockade on Morphine Consumption, Pain and Mobilisation After Total Knee Arthroplasty Phase IV: RCT, safety/efficacy study NCT01104883 The Subvastus Approach in Total Knee Arthroplasty Phase IV: RCT NCT00346788 A Comparative Study of Knee Systems Phase IV: RCT NCT01331278 275 Adt Sep-09 Mar-11 Foundation for Sen Southwest Orthopedic Research http://ClinicalTrials.gov/show/NCT01331278 Does intramedullary plugging Intramedullary reduce blood transfusion plugging with requirements in total knee retransfusion drains; replacement? Retransfusion drains RCT only ISRCTN94713892 Management of Postoperative Procedure: Pain Following Total Knee acupunctureArthroplasty by Using moxibustion therapy; Acupuncture-moxibustion Therapy Procedure: Regular Phase II/III: RCT therapy NCT01047384 Short- Versus Long-duration Procedure: Long Tourniquet Use During Total Knee duration tourniquet; Replacement (TKR) Procedure: Short RCT, safety/efficacy study duration tourniquet NCT01162720 Tibial Nerve Versus Sciatic Nerve Procedure: Selective Block Tibial Nerve block; RCT Procedure: Sciatic NCT01415193 Nerve Block A Comparison Between an Procedure: Limb Individual Low Tourniquet occlusion pressure Pressure Versus a Standard (LOP); Procedure: Pressure During Total Knee conventional Arthroplasty measurement RCT, efficacy study method NCT01442298 Effect of Ambulatory Continuous Procedure: Femoral Nerve Blocks on Ambulatory Readiness-for-Discharge Following continuous femoral Total Knee Replacement nerve block for 100 RCT, efficacy study hours NCT00419276 Primary total knee Comp replacement surgery 100 Adt Dec-09 Jan-11 Royal Berkshire http://www.controlledSen NHS Foundation trials.com/ISRCTN9471389 Trust (UK) Osteoarthritis, Knee Not yet 100 Rec Adt Jan-10 Jan-11 Chang Gung Sen Memorial Hospital http://ClinicalTrials.gov/show/NCT01047384 Arthroplasty, Replacement, Knee Term 65 Adt Nov-08 Dec-10 Fairfield Sen Hospital, Australia http://ClinicalTrials.gov/show/NCT01162720 Post Operative Analgesia; TKA Comp 80 Adt Mar-09 Dec-10 Saint Francis Sen Care http://ClinicalTrials.gov/show/NCT01415193 Complications; Arthroplasty Comp 164 Child Oct-08 Oct-10 Charlotta Adt Olivecrona Sen Total Knee Arthroplasty Comp 81 276 http://ClinicalTrials.gov/show/NCT01442298 Adt Apr-07 Aug-10 National Institute http://ClinicalTrials.gov/show/NCT00419276 Sen of General Medical Sciences (NIGMS); University of Florida; University of California, San Diego; Stryker Instruments Sub-Vastus Versus Mid-Vastus Arthrotomy for Total Knee Arthroplasty: a Randomized Clinical Trial RCT, efficacy study NCT00925626 Does Tourniquet Use in Total Knee Replacement Improve Fixation Phase III: RCT NCT01470482 Procedure: SubVastus arthrotomy; Procedure: Mid Vastus arthrotomy Susp 100 Adt Jun-09 Aug-10 University http://ClinicalTrials.gov/show/NCT00925626 Sen Hospital, Ghent Comp 50 Adt Aug-06 May-10 Per Aspenberg Sen Osteoarthritis Rec 162 Adt Sen Thromboembolism; Arthroplasty, Knee; Arthroplasty, Hip Rec Procedure: No use of Osteoarthritis, Knee tourniquet; Procedure: Tourniquet Other Progressive Rehabilitation Other: Total knee Following Total Knee Arthroplasty replacement Phase I: RCT, safety/efficacy rehabilitation study NCT01537328 Genetics Informatics Trial (GIFT) of Warfarin to Prevent DVT Phase III: RCT, safety/efficacy study NCT01006733 Tricompartmental Gonarthrosis Other: Pharmacogenetic Warfarin Initiation; Other: Clinical Warfarin Initiation (nonpharmacogenetic); Other: Pharmacogenetic Warfarin Initiation; Other: Clinical Warfarin Initiation (nonpharmacogenetic) http://ClinicalTrials.gov/show/NCT01470482 Jul-11 May-17 University of http://ClinicalTrials.gov/show/NCT01537328 Colorado, Denver; National Institutes of Health; Eunice Kennedy Shriver National Institute of Child Health and Human Development 1600 Adt Mar-11 Aug-15 Washington http://ClinicalTrials.gov/show/NCT01006733 Sen University School of Medicine; Intermountain Health Care, Inc.; University of Utah; Hospital for Special Surgery, New York; National Heart, Lung, and Blood Institute (NHLBI) 277 Structured Treatment of Osteoarthritis of the Knee With or Without Total Knee Replacement RCT, efficacy study NCT01410409 Other: Osteoarthritis of the Neuromuscular Knee training (NEMEXTJR); Drug: Paracetamol; Drug: Burana; Drug: Pantoprazol; Behavioral: Dietary counseling; Behavioral: Patient education; Procedure: TKR; Other: Insoles The Difference Between Other: Rehabilitation Osteoarthritis, Knee Rehabilitation With or Without with strength training; Strength Training After Total Knee Other: Rehabilitation Replacement without strength Phase II/III: RCT, safety/efficacy training study NCT01351831 Visionaire™ Versus Standard Other: Total Knee Degenerative Instrumentation Safety and Arthroplasty; Other: Arthritis of Knee Efficacy in Total Knee Arthroplasty Total Knee (TKA) Arthroplasty RCT, safety/efficacy study NCT01084772 A Randomized Prospective Trial of Other: Instrument Osteoarthritis, Knee Total Knee Arthroplasty Options Comparing Standard Knee Cutting Guides and MRI Generated Patient Specific Custom Cutting Guides RCT NCT01072019 Efficacy and Safety of FLOSEAL Other: Standard of Knee Replacement for Hemostasis in Total Knee Care; Drug: Surgery; Arthroplasty FLOSEAL Osteoarthritis Phase IV: RCT, safety/efficacy Hemostatic Matrix study NCT01410240 Rec 100 Child Sep-11 Apr-14 Northern Adt Orthopaedic Sen Division, Denmark http://ClinicalTrials.gov/show/NCT01410409 Rec 70 Adt Jan-11 Aug-13 Copenhagen Sen University Hospital, Hvidovre http://ClinicalTrials.gov/show/NCT01351831 Rec 196 Child Apr-10 Jun-13 Smith & Adt Nephew, Inc. Sen http://ClinicalTrials.gov/show/NCT01084772 Invite 165 Adt Mar-10 Mar-13 Washington Sen University School of Medicine; Biomet, Inc. http://ClinicalTrials.gov/show/NCT01072019 Rec 138 Adt Sep-11 Jan-13 Baxter Sen Healthcare Corporation http://ClinicalTrials.gov/show/NCT01410240 278 Improving Function After Knee Arthroplasty With Weight-Bearing Biofeedback Phase I: RCT NCT01333189 POMX (Post Operative Morbidity): Randomized controlled trial of chewing gum to reduce postoperative morbidity in elective orthopaedic surgery RCT, efficacy study ISRCTN20301599 A Comparison of Sartorius Vs. Quadriceps Evoked Motor Response for Femoral Nerve to Prevent Secondary Catheter Failure RCT, safety/efficacy study NCT01313546 Rehabilitation After Fast-track Total Knee Arthroplasty RCT NCT01329081 The Effectiveness of 8-weeks Progressive Strength Training to Patients With Unicompartmental Knee Replacement, Initiated Within the First Postoperative Week Phase III: RCT NCT01345825 Gamma Vacuum Foil (GVF) Versus Cross-linked Polyethylene in Total Knee Arthroplasty Study Phase IV: RCT, safety/efficacy study NCT00289133 Progressive Exercise After Total Knee Arthroplasty (TKA) RCT, efficacy study NCT00605124 Other: WeightArthropathy of Knee bearing biofeedback Joint exercise; Other: Standard of care exercise Chewing gum Elective orthopaedic hip and knee arthroplasty procedures Rec 20 Adt Jan-11 Dec-12 University of Sen Colorado, Denver Active 106 Adt Sep-11 Sep-12 University http://www.controlledSen College London trials.com/ISRCTN20301599 (UK) Other: Stimulation of Arthroplasty, quariceps muscle Replacement, Knee Not yet Rec 40 Adt May-11 Sep-12 Sunnybrook http://ClinicalTrials.gov/show/NCT01313546 Sen Health Sciences Centre Other: Postoperative Knee Arthroplasty rehabilitation after fast-track TKA; Other: Postoperative rehabilitation after fast-track TKA Other: Resistance Knee Osteoarthritis training Rec 140 Adt Apr-10 Jul-12 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT01329081 Rec 60 Adt Mar-11 Jul-12 University of Sen Aarhus http://ClinicalTrials.gov/show/NCT01345825 Other: total knee Osteoarthritis, Knee; Active, arthroplasty; Device: Arthritis, Rheumatoid NR total knee arthroplasty 937 Adt Feb-05 Jun-12 DePuy Sen Orthopaedics http://ClinicalTrials.gov/show/NCT00289133 Other: Knee muscle Osteoarthritis exercises 120 Adt Jan-08 Apr-12 Jyväskylä http://ClinicalTrials.gov/show/NCT00605124 Sen Central Hospital Rec 279 http://ClinicalTrials.gov/show/NCT01333189 Comparison of Surgical Time and Efficiency of Total Knee Arthroplasty Prospective, case control study NCT01301950 Long Term Follow-up of the “Stryker Dacron and Trevira Ligament” for Anterior Cruciate Ligament (ACL) Repair" Prospective, cohort study NCT01138696 Effect of Physiotherapy After Total Knee Replacement RCT, efficacy study NCT00807716 Role of Bone in Knee Osteoarthritis (OA) Prospective, cohort study NCT00850538 Preoperative Exercise in Patients Undergoing Total Hip or Knee Replacement RCT NCT01003756 Other: Instrument Osteoarthritis, Knee Rec 30 Adt May-10 Mar-12 DePuy Sen Orthopaedics Other: Questionnaires; Other: RX ACL Rupture; Replacement Rec 80 Adt Feb-10 Dec-11 University http://ClinicalTrials.gov/show/NCT01138696 Sen Hospital, Ghent Active, NR 72 Adt Oct-08 Dec-11 University of Sen Oslo http://ClinicalTrials.gov/show/NCT00807716 Rec 95 Adt Sen http://ClinicalTrials.gov/show/NCT00850538 Comp 165 Other: task oriented Total Knee exercises Arthroplasty Radiation: MRI; Osteoarthritis, Knee Procedure: Primary Total Knee Replacement Other: Preoperative Osteoarthritis neuromuscular exercise Effectiveness of in-home telerehabilitation service following knee arthroplasty RCT ISRCTN66285945 Effects of Kneehab 12-week Perioperative Total Knee Arthroplasty Phase III: RCT, safety/efficacy study NCT01096524 In-home telerehabilitation; face-to-face home rehabilitation Total knee arthroplasty Comp 204 Other: Standard Physiotherapy; Device: Kneehab Knee Osteoarthritis; Disuse Atrophy Invite 200 Transfusion Requirements in Orthopedic Surgery (PHASE 2) Prospective, cohort study NCT00726349 Other: No intervention Total Hip or Knee Arthroplasty Comp 305 280 Jul-08 Oct-11 The New England Baptist Hospital; Genzyme Adt Nov-09 Aug-11 University of Sen Southern Denmark; Odense University Hospital Adt Sep-09 Aug-11 Laval University Sen (Canada) http://ClinicalTrials.gov/show/NCT01301950 http://ClinicalTrials.gov/show/NCT01003756 http://www.controlledtrials.com/ISRCTN66285945 Adt Mar-10 Jul-11 Bio-Medical http://ClinicalTrials.gov/show/NCT01096524 Sen Research, Ltd.; Royal Liverpool and Broadgreen University Hospitals NHS Trust Adt May-08 May-11 Centre http://ClinicalTrials.gov/show/NCT00726349 Sen hospitalier de l'Université de Montréal (CHUM) Cost-Effectiveness of Web-Based Other: in-person; Follow Ups Other: web-based RCT, safety/efficacy study NCT01079572 Arthroplasty, Replacement, Hip; Arthroplasty, Replacement, Knee Manual Lymphatic Drainage Other: Manual Total Knee Joint Following Total Knee Arthroplasty lymphatic drainage; Prosthesis Surgery Other: relaxation RCT, efficacy study NCT00711711 Rec 1000 Child Feb-10 Mar-11 University of http://ClinicalTrials.gov/show/NCT01079572 Adt Western Ontario, Sen Canada; The Physicians' Services Incorporated Foundation Comp 60 Child Jun-08 Mar-11 Haute Ecole http://ClinicalTrials.gov/show/NCT00711711 Adt Cantonale Sen Vaudoise de Santé; University of Applied Sciences of Western Switzerland; University of Lausanne Hospitals Comp 75 Adt Oct-09 Mar-11 DePuy http://ClinicalTrials.gov/show/NCT01108237 Sen Orthopaedics Alignment Comparison Between TruMatch™ Personalized Solutions and Conventional Total Knee Replacement Instrumentation Single group assignment, efficacy study NCT01108237 Knee Joint Icing and Kneeextension Strength Phase I: RCT, efficacy study NCT01249612 Other: TruMatch™ Personalized Solutions Osteoarthritis, Knee Other: Thermotherapy; Other: Thermotherapy Arthroplasty Active, NR 20 I-ONE therapy in patients undergoing total knee arthroplasty RCT ISRCTN10526056 The Efficacy of Automated Intermittent Boluses for Continuous Femoral Nerve Block: a Prospective, Randomized Comparison to Continuous Infusions RCT, efficacy study NCT01226927 I-ONE therapy (Biophysical stimulation); usual care post-operatively Other: Automated intermittent bolus Total knee arthroplasty Comp 30 Arthroplasty, Comp Replacement, Knee; Nerve Block 45 281 Adt Apr-10 Dec-10 Hvidovre Sen University Hospital; Lundbeck Foundation Adt Jan-08 Jun-10 IGEA (Italy) Sen http://ClinicalTrials.gov/show/NCT01249612 Adt Apr-09 Apr-10 Medical Sen University of South Carolina http://ClinicalTrials.gov/show/NCT01226927 http://www.controlledtrials.com/ISRCTN10526056 Miscellaneous observational studies Comparison of Functional Outcomes of Three Surgical Approaches in Knee Arthroplasty Prospective, case control study NCT00983762 Early Clinical Results of MobileBearing Revision Total Knee Arthroplasty Retrospective, case-only study NCT01398800 A Clinical Investigation of the Vanguard™ Complete Knee System Prospective, cohort study NCT00698854 DePuy Revision TKA Implant 5yr Survivorship Retrospective, case-only study NCT01245478 Joint Stiffness Following Knee Replacement Surgery Retrospective, case control study NCT00664651 Prediction of Outcomes Following Total Knee Replacement Prospective, cohort study NCT01370421 Length of Stay and Complications in High-risk Patients Receiving Fast-track Total Hip (THA) or Knee- Alloplasty (TKA) Prospective, cohort study NCT01515670 Knee Osteoarthritis Term 12 Adt Jun-09 Jan-20 Massachusetts Sen General Hospital; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT00983762 Arthroplasty, Replacement, Knee Rec 320 Child Jul-11 Dec-18 Colorado Joint Adt Replacement; Sen DePuy Orthopaedics http://ClinicalTrials.gov/show/NCT01398800 Osteoarthritis; Traumatic Arthritis; Rheumatoid Arthritis Invite 600 http://ClinicalTrials.gov/show/NCT00698854 Knee Arthroplasty Active, NR 0 Joint Contracture Rec 120 Osteoarthritis Rec 200 Arthroplasty Complications; Preoperative Comorbidity; Postoperative Morbidity Rec Adt Mar-04 Jan-17 Biomet, Inc. Sen Adt Nov-10 Dec-16 The New http://ClinicalTrials.gov/show/NCT01245478 Sen England Baptist Hospital; Depuy, Inc. Adt Dec-06 Dec-15 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00664651 Sen Research Institute Adt Apr-11 Dec-15 Brigham and Sen Women's Hospital 30000 Adt Sen 282 http://ClinicalTrials.gov/show/NCT01370421 Feb-10 Jan-15 Rigshospitalet, http://ClinicalTrials.gov/show/NCT01515670 Denmark; Hvidovre University Hospital; Aarhus University Hospital; Vejle Hospital; Sydvestjysk Hospital; Holstebro Hospital Why Are so Many Patients Dissatisfied With Knee Replacement Surgery? Exploring Variations of the Patient Experience Prospective, cohort study NCT01466920 Analysis of Standard Versus Barbed Sutures in Primary Total Knee Arthroplasty. Cross-sectional, cohort study NCT01320371 Evaluation of Weight Bearing After Total Hip and Knee Replacement Prospective, cohort study NCT01135160 Evaluation of Patellar Crepitus Prospective, case control study NCT01340144 Feasibility of Outpatient Total Knee Arthroplasty Prospective, cohort study NCT01186211 Pradaxa (Dabigatran Etexilate) 150 mg/q.d. in Patients With Moderate Renal Impairment After Hip or Knee Replacement Surgery Prospective, cohort study NCT00847301 Preopioid Versus Nonopioid in Total Knee Arthroplasty (TKA) Prospective, cohort study NCT01323179 Pain and Analgesic Consumption Compared Between the First and the Second Surgery in Staged BTKRA Prospective study NCT01457313 Total Knee Arthroplasty Arthropathy of Knee Arthroplasty, Replacement, Hip; Total Knee Arthroplasty Arthroplasty, Replacement, Knee Total Knee Replacement Not yet 500 Rec Invite 200 Adt Nov-11 Jan-15 University of http://ClinicalTrials.gov/show/NCT01466920 Sen British Columbia Adt Jan-11 Dec-14 University of Sen Utah Not yet 200 Child Aug-12 Dec-13 Kantonsspital Rec Adt Münsterlingen Sen http://ClinicalTrials.gov/show/NCT01320371 http://ClinicalTrials.gov/show/NCT01135160 Active, 1250 Child Apr-11 Sep-13 Colorado Joint http://ClinicalTrials.gov/show/NCT01340144 NR Adt Replacement Sen Rec 60 Adt Nov-10 Jul-13 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01186211 Sen Research Institute Arthroplasty, Replacement; Thromboembolism Rec 500 Adt Apr-09 Apr-13 Boehringer http://ClinicalTrials.gov/show/NCT00847301 Sen Ingelheim Pharmaceuticals Postoperative Pain Rec 180 Adt Mar-11 Dec-12 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01323179 Degenerative Arthritis Rec 30 Adt Oct-11 Nov-12 Seoul National Sen University Bundang Hospital http://ClinicalTrials.gov/show/NCT01457313 283 Changes of the Single Limb Standing Balance After Total Knee Arthroplasty in Degenerative Osteoarthritis Prospective, case-only study NCT01192334 Comparison of Clinical Outcomes and Performance of Total Knee Replacement Patients Before and After Surgery Prospective, case control study NCT01379118 Perioperative Hyperglycaemia in Primary Total Hip and Knee Replacement Prospective, cohort study NCT01021826 Comparison of Kinematics for Subjects Implanted With a PFC Sigma Rotating Platform or Fixed Bearing Total Condylar III Prothesis Retrospective, case control study NCT01290640 In Vivo Determination of 3D Patellofemoral Mechanics Retrospective, case-only study NCT01290627 Prospective Study Measuring Clinical Outcomes of Knee Arthroplasty Using the OrthoSensor Surgical Smart Trial Prospective, cohort study NCT01469299 Preoperative Pain, Function, and Activity for Total Hip and Knee Arthroplasty Patients Prospective, cohort study NCT01248039 Knee Osteoarthritis Rec 50 Degenerative Joint Not yet 50 Disease; Rec Osteoarthritis; Knee Injury, Trauma; Connective Tissue Disorder; Pain; Loss of Function Knee Replacement; Active, 200 Hip Replacement; NR Hyperglycemia Knee Prosthesis; Knee Arthroplasty Not yet Rec 30 Arthoplasty Replacement Knee; Knee Prosthesis Not yet Rec 40 Osteoarthritis, Knee Rec 500 Arthroplasty Rec 100 284 Child Sep-10 Oct-12 Ulsan University http://ClinicalTrials.gov/show/NCT01192334 Adt Hospital Sen Adt Sen Jul-11 Oct-12 Loma Linda University http://ClinicalTrials.gov/show/NCT01379118 Adt Dec-09 Jul-12 Coxa, Hospital http://ClinicalTrials.gov/show/NCT01021826 Sen for Joint Replacement; University of Tampere Adt Feb-11 Feb-12 The University of http://ClinicalTrials.gov/show/NCT01290640 Sen Tennessee Knoxville; DePuy Orthopaedics Adt Feb-11 Feb-12 The University of http://ClinicalTrials.gov/show/NCT01290627 Sen Tennessee Knoxville; DePuy Orthopaedics Adt Oct-11 Jan-12 Orthosensor, http://ClinicalTrials.gov/show/NCT01469299 Sen Inc. Adt Jan-11 Jan-12 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT01248039 Study of Surgical Technique With Use of Single-radius Prosthesis in Total Knee Replacement Cross-sectional study NCT01505452 Surgical Field Bacterial Contamination in Primary Total Hip (THA) and Knee (TKA) Arthroplasty Prospective, cohort study NCT01493375 Arthritis of Knee Tissue Culture Versus Swab Culture in Prosthetic Joint Infections Prospective, cohort study NCT01482533 Systemic Inflammation Versus Acute Pain in Total Knee Arthroplasty (TKA) Prospective, cohort study NCT01322074 A Comparison of Wear Among Mobile and Fixed Bearing Knee Replacements Retrospective, case control study NCT01165957 Postoperative Sleep Disturbances Role in Cognitive Test Results After Fast-track Hip and Knee Arthroplasty Prospective study NCT01383369 Comparison of Stability and Outcomes in Single-radius Femoral Component for Total Knee Arthroplasty Prospective, cohort study NCT01379755 Revision Total Hip Not yet N/K Arthroplasty; Rec Revision Total Knee Arthroplasty Prosthetic Infections Rec 30 Comp 60 Adt Nov-11 Jan-12 Athens http://ClinicalTrials.gov/show/NCT01505452 Sen Orthopedic Clinic, P.A.; Stryker Orthopaedics Adt Jun-10 Dec-11 Northern http://ClinicalTrials.gov/show/NCT01493375 Sen Orthopaedic Division, Denmark; Aarhus University Hospital; University of Aarhus; Aalborg University Adt N/K Nov-11 Rothman http://ClinicalTrials.gov/show/NCT01482533 Sen Institute Orthopaedics Other Acute Comp Postoperative Pain; Systemic Inflammatory Response Syndrome Osteoarthritis Invite 120 Adt Aug-09 Oct-11 Hvidovre Sen University Hospital 26 Adt Jun-10 Oct-11 Anderson http://ClinicalTrials.gov/show/NCT01165957 Sen Orthopaedic Research Institute; DePuy Orthopaedics Postoperative Cognitive Abilities Comp 20 Adt Feb-11 Aug-11 Rigshospitalet, Sen Denmark http://ClinicalTrials.gov/show/NCT01383369 Osteoarthritis Active, NR 213 Adt Aug-10 Jul-11 Chonnam Sen National University Hospital http://ClinicalTrials.gov/show/NCT01379755 285 http://ClinicalTrials.gov/show/NCT01322074 Comp 5476 Adt Feb-09 Jul-11 Boehringer http://ClinicalTrials.gov/show/NCT00846807 Sen Ingelheim Pharmaceuticals Pradaxa (Dabigatran Etexilate) 220 mg/q.d. in the General Population After Hip or Knee Replacement Surgery Prospective, cohort study NCT00846807 Daptomycin With Rifampin for Treatment of Staphylococcal Prosthetic Joint Infection Prospective, cohort study NCT01144000 Arthroplasty, Replacement; Thromboembolism Effect of Rivaroxaban on Coagulation Parameters- an ex Vivo Study Retrospective, cohort study NCT00986635 Differences in Comp 100 Laboratory Coagulation Parameters; hip or knee replacement surgery Effect of Dabigatran Comp 70 in Laboratory Coagulation Parameters; hip or knee replacement surgery Total Knee Not yet 40 Replacement Rec Effect of Dabigatran on Coagulation parameters-an ex Vivo Study Retrospective, cohort study NCT01112202 Biochemical Approach to Measuring Surgical Trauma Prospective, cohort study NCT01037400 VISIONAIRE™ Value Study Prospective, cohort study NCT01107769 Recovery at the Post Anaesthetic Care Unit After Hip and Knee Arthroplasty Prospective, cohort study NCT01178489 Staphylococcal Not yet Infections; Rec Prosthesis; hip, knee and shoulder Prosthetic Joint Infection (PJI) 60 Adt Sep-10 Jun-11 Centre http://ClinicalTrials.gov/show/NCT01144000 Sen Hospitalier Universitaire Vaudois; University of Lausanne Hospitals; Kantonsspital Liestal; Schulthess Klinik Adt Sep-09 Apr-11 Johann http://ClinicalTrials.gov/show/NCT00986635 Sen Wolfgang Goethe University Hospitals Adt Apr-10 Apr-11 Johann Sen Wolfgang Goethe University Hospitals http://ClinicalTrials.gov/show/NCT01112202 Adt Feb-10 Feb-11 Hamilton Health http://ClinicalTrials.gov/show/NCT01037400 Sen Sciences Corporation Osteoarthritis of the Knee Comp 38 Adt Apr-10 Feb-11 Smith & Sen Nephew, Inc. http://ClinicalTrials.gov/show/NCT01107769 PACU Stay After THA Under Spinal Anaesthesia; PACU Stay After TKA Under Spinal Anaesthesia Comp 170 Adt Aug-10 Jan-11 Hvidovre Sen University Hospital http://ClinicalTrials.gov/show/NCT01178489 286 Why in Hospital - Factors Determining Time to Discharge Readiness After Arthroplasty Surgery Prospective, case-only study NCT01047371 Early Outcome Assessment of Revision Total Knee Arthroplasty Using Metaphyseal Sleeves Retrospective, cohort study NCT01156558 Early Migration in a High Congruent Rotating Platform Total Knee Prosthesis Design Prospective, cohort study NCT01102829 Study to Evaluate the Safety and Efficacy of Pradaxar for the Prevention of Venous Thromboembolism in the Mexican Population Undergoing Elective Total Hip or Knee Replacement Surgery Prospective, cohort study NCT00967447 Pain; Nausea; Comp Vomiting; Dizzyness; Fatigue; Organizational Concerns; Ect.; Arthroplasty, Hip; Arthroplasty, Knee Revision Total Knee Comp Replacement 200 Rheumatoid Arthritis Comp 11 Thromboembolism; Arthroplasty, Replacement, Hip Term Adt Jan-10 Aug-10 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT01047371 Adt Jun-10 Jul-10 Rothman Sen Institute Orthopaedics; DePuy Orthopaedics Child Sep-07 Apr-10 Leiden Adt University Sen Medical Center http://ClinicalTrials.gov/show/NCT01156558 http://ClinicalTrials.gov/show/NCT01102829 Adt Feb-09 Mar-10 Boehringer http://ClinicalTrials.gov/show/NCT00967447 Sen Ingelheim Pharmaceuticals 287 A9G: OTHER Title Phases: trial design (control) CT ID Behavioural Early Intervention for Adolescents With Patellofemoral Pain Syndrome RCT, efficacy study NCT01438762 Interventions Conditions Behavioral: Patient information and education; Other: Information, education and physiotherapy Patellofemoral Pain Syndrome Rec Gait Retraining to Reduce Knee Osteoarthritis Pain Phase I/II: Single group assignment, safety/efficacy study NCT01397981 Supporting Decision Making for Musculoskeletal PreferenceSensitive Care RCT NCT01345123 Behavioral: Gait retraining Osteoarthritis, Knee Rec Behavioral: Provision Knee Pain Chronic; of condition specific Arthritis (Hip); DVD and Pamphlet Arthritis (Knee); to support Shared Back Pain Decision Making; Behavioral: Telephonic outreach and support by Health Coach; Behavioral: No condition specific telephonic outreach Educational Intervention for Knee Behavioral: Decision Osteoarthritis Pain Aid Video; RCT, efficacy study Behavioral: NCT00324857 Motivational Interviewing Recruit n Age Start (Grp) Date End Sponsors Date URL 102 Child Jun-11 Sep-14 Michael Skovdal http://ClinicalTrials.gov/show/NCT01438762 Adt Rathleff; University of Southern Denmark; Aarhus University Hospital 25 Adt Jul-11 May-12 Stanford http://ClinicalTrials.gov/show/NCT01397981 Sen University Active, 1800 Adt Feb-11 Mar-12 Health Dialog; http://ClinicalTrials.gov/show/NCT01345123 NR 0 Sen Foundation for Informed Medical Decision Making; University of Massachusetts, Boston Comp 600 288 Adt Sep-06 Sep-11 Department of http://ClinicalTrials.gov/show/NCT00324857 Sen Veterans Affairs Device iUni Foundation Study Phase IV: Single group assignment, safety/efficacy study NCT01117571 Gold Against Pains From Osteoarthrosis in the Knee Phase II: RCT, efficacy study NCT00378339 Study of IN.PACT Amphirion™ Drug Eluting Balloon vs. Standard PTA for the Treatment of Below the Knee Critical Limb Ischemia RCT, safety/efficacy study NCT00941733 Research in Osteoarthritis in Manchester (ROAM) Brace RCT ISRCTN50380458 Hymovis™ Versus Placebo in Knee Osteoarthritis Phase III: RCT, safety/efficacy study NCT01372475 Compass Hinge Stabilization of Knee Dislocations: A Randomized Trial RCT, efficacy study NCT00582517 Device: iUni® Unicompartmental Knee Resurfacing Device Osteoarthritis Device: gold berlocks Arthritis Device: IN.PACT Amphirion; Device: Standard PTA balloon Chronic Critical Limb Ischemia Brace Patellofemoral pain Device: Hymovis Knee Osteoarthritis Intra-articular Injection; Procedure: Phosphate Buffered Saline Injection Device: Compass Knee Dislocation Universal Hinge External Fixator; Procedure: Noninvasive External Knee Brace Effectiveness Study of the Ivivi Device: Ivivi Knee Osteoarthritis SofPulse for Pain Amelioration in SofPulse; Device: Adults With Mild to Moderate Knee Ivivi SofPulse Osteoarthritis Phase IV: RCT, efficacy study NCT01457742 Rec 200 Adt Apr-10 Dec-20 ConforMIS, Inc. http://ClinicalTrials.gov/show/NCT01117571 Sen Wdrwn 50 Rec 357 Adt Jan-09 Dec-15 Northern http://ClinicalTrials.gov/show/NCT00378339 Sen Orthopaedic Division, Denmark; University of Aarhus; Aarhus University Hospital Adt Sep-09 Dec-15 Invatec S.p.A. http://ClinicalTrials.gov/show/NCT00941733 Sen Active 144 Adt Aug-09 Mar-13 University of http://www.controlledSen Manchester (UK) trials.com/ISRCTN50380458 Rec 800 Adt Mar-11 Jan-13 Fidia Sen Farmaceutici s.p.a. http://ClinicalTrials.gov/show/NCT01372475 Active, NR 109 Adt Aug-00 Dec-12 University of Sen Alabama at Birmingham; Smith & Nephew, Inc. http://ClinicalTrials.gov/show/NCT00582517 Rec 150 Adt Oct-11 Oct-12 Amp http://ClinicalTrials.gov/show/NCT01457742 Sen Orthopedics, Inc. 289 The Efficacy of Device: Synvisc One Knee Osteoarthritis Viscosupplementation for Early Knee Osteoarthritis RCT NCT01210742 A Study Comparing Device: Hylan G-F Osteoarthritis, Knee Viscosupplementation and 20 (Synvisc One); Corticosteroid Injections for Knee Drug: Osteoarthritis Methylprednisolone RCT, efficacy study (Corticosteroid) NCT01132677 Investigation of Sodium Device: Sodium Osteoarthritis of the Hyaluronate for Treatmet of Painful Hyaluronate; Device: Knee Chronic Osteoarthritis of the Knee Buffered Saline Phase III: RCT, safety/efficacy study NCT00988091 Negative Pressure Wound Device: V.A.C. by Surgical Wound Dressing Study K.C.I. Infection RCT, efficacy study NCT01366105 The effectiveness of Shoes and Barefoot walking; Medial knee OA Insoles on the Loading at the Knee Mobility shoe in subjects with knee osteoarthritis designed to mimic RCT barefoot walking; ISRCTN83706683 Control shoe; Control shoe with unsupported lateral wedge; Control shoe with salford wedge Position HTO Multicenter NIS Device: Position Medial Prospective, cohort study HTO system Monocompartmental NCT00889304 Osteoarthritis of the Knee Safety and Effectiveness Study of Device: MONOVISC Osteoarthritis Hyaluronic Acid for Osteoarthritis of the Knee RCT, safety/efficacy study NCT00653432 Not yet Rec 60 Adt Dec-10 Oct-12 University of Sen Oxford Invite 78 Adt May-10 Dec-11 LifeMark Health http://ClinicalTrials.gov/show/NCT01132677 Sen Comp 596 Adt Sep-09 Apr-11 Ferring http://ClinicalTrials.gov/show/NCT00988091 Sen Pharmaceuticals Comp 106 Adt Aug-08 Oct-10 Georgetown Sen University http://ClinicalTrials.gov/show/NCT01366105 Comp 50 Adt Aug-09 Aug-10 University of Sen Salford (UK) http://www.controlledtrials.com/ISRCTN83706683 Comp 221 Adt Sen Jul-07 Jun-10 Aesculap AG http://ClinicalTrials.gov/show/NCT00889304 Comp 350 Adt Jan-08 Feb-10 Anika Sen Therapeutics, Inc. http://ClinicalTrials.gov/show/NCT00653432 290 http://ClinicalTrials.gov/show/NCT01210742 Dietary supplement Zurich Multiple Endpoint Vitamin D Dietary Supplement: Knee Osteoarthritis Trial in Knee OA Patients Vitamin D3 Phase IV: RCT, efficacy study (cholecalciferol) NCT00599807 Drugs including biologics Effect of Gabapentin on Orthopedic Pain Phase IV: RCT, efficacy study NCT01546857 Clonidine in Femoral Nerve Block Surgery in Children Phase II: RCT, safety/efficacy study NCT01293149 Biological Response of Stage IV Knee Osteoarthritis to Serial 12.5% Dextrose Phase II/III: Single group assignment, efficacy study NCT01210183 Effectiveness of Two Types of Treatment in Restoring Muscle After Hip or Knee Surgery Phase II: RCT, efficacy study NCT00393848 Safety, Tolerability and Pharmacokinetics of SAR113945 in Japanese Patients With Knee Osteoarthritis Phase I: RCT, safety study NCT01511549 Drug: Placebo; Drug: Degenerative Joint Gapabentin Disease of Hip and Knee. Drug: Ropivacaine; Drug: Clonidine Other Reconstructive Surgery Drug: Dextrose intraarticularly administered Knee Osteoarthritis Drug: Essential amino acid supplement; Drug: Ketoconazole; Drug: Whey protein Hip Fracture; Osteoarthritis; Femur Head Necrosis Drug: placebo; Drug: Knee Osteoarthritis SAR113945 Rec 287 Adt Jan-08 May-14 University of http://ClinicalTrials.gov/show/NCT00599807 Sen Zurich; Harvard School of Public Health; Tufts University; Boston University Rec 90 http://ClinicalTrials.gov/show/NCT01546857 Adt Mar-12 Dec-14 University of Sen Medicine and Dentistry New Jersey Not yet 150 Child Apr-11 Mar-13 Nationwide Rec Adt Children's Hospital Rec 12 Adt Sen Active, NR 120 Rec 24 Adt Oct-06 Oct-12 University of http://ClinicalTrials.gov/show/NCT00393848 Sen Arkansas; National Institute of Arthritis and Musculoskeletal and Skin Diseases Adt Jan-12 Sep-12 Sanofi-Aventis http://ClinicalTrials.gov/show/NCT01511549 Sen 291 Jul-10 Dec-12 Universidad Nacional de Rosario http://ClinicalTrials.gov/show/NCT01293149 http://ClinicalTrials.gov/show/NCT01210183 Evaluation of the Effect of Adding Drug: Hylan GF-20 Corticosteroid to alone; Drug: Viscosupplementation Triamcinolone Phase IV: RCT, safety/efficacy study NCT01335321 TArgeting Synovitis in Knee osteoarthritis (OA) Single group assignment, efficacy study ISRCTN07329370 Study of Viscosupplementation for the Treatment of Knee Pain After Menisectomy RCT, efficacy study NCT00971074 The Efficacy and Safety of Intraarticular Sodium Hyaluronate (Hyalgan) After Proximal Tibial Osteotomy in Treatment of Knee Osteoarthritis Patients Phase II: RCT, safety/efficacy study NCT01267214 Safety, Tolerability and Pharmacokinetics of SAR113945 Following Intra-articular Administration in Patients With Knee Osteoarthritis Phase I: RCT, safety study NCT01113333 Osteoarthritis Aspiration + injection Knee Osteoarthritis 80mg methylprednisolone acetate (Depo-Medrone). Drug: Hylan G-F 20; Arthralgia Drug: Sham Injection Drug: Sodium Hyaluronate (Hyalgan); Other: Osteotomy alone Knee Osteoarthritis Drug: placebo; Drug: Osteoarthritis SAR113945 Rec 108 Active 120 Rec 252 Adt Dec-09 Dec-11 Ohio State University; Genzyme Comp 40 Adt Feb-09 Jul-11 TRB Chemedica http://ClinicalTrials.gov/show/NCT01267214 Comp 40 Adt Apr-10 Feb-11 Sanofi-Aventis Sen 292 Adt Mar-11 Jul-12 University of Sao http://ClinicalTrials.gov/show/NCT01335321 Sen Paulo General Hospital; Fundação de Amparo à Pesquisa do Estado de São Paulo Adt May-10 May-12 Salford Royal http://www.controlledSen NHS Foundation trials.com/ISRCTN07329370 Trust (UK) http://ClinicalTrials.gov/show/NCT00971074 http://ClinicalTrials.gov/show/NCT01113333 TENDOSHOCK-2010 Combination Drug: Polidocanol; Tendinopathy; Therapy for Athletic Device: Focused Epicondylitis; Tendinopathies extracorporeal shock Achilles, Patella, Phase II: Single group wave therapy; Drug: Elbow assignment, safety/efficacy Topical NO; study Behavioral: Painful NCT01185951 eccentric training in Achilles tendinopathy; Behavioral: Painful eccentric training for patella tendinopathy on 25° decline board; Behavioral: Painful eccentric training for elbow tendinopathy using Thera-Band Flex-Bar Procedure Oxford Partial Knee Comparative Instrument Pilot Study Non-randomized, parallel assignment NCT01410786 Optimisation of the Treatment of Infectious Bursitis Phase III: RCT, safety/efficacy study NCT01406652 A Comparison of Manual Physical Therapy and Corticosteroid Injections for Knee Osteoarthritis RCT, efficacy study NCT01427153 Active, NR 114 Procedure: Osteoarthritis, Knee Not yet 70 Conventional Rec Instrumentation; Procedure: Signature Custom Guides Procedure: TwoOlecranon Bursitis; Rec 240 stage bursectomy Patellar Bursitis Procedure: Orthopaedic manual physical therapy; Procedure: Corticosteroid Injection Comparison of Autologous Procedure: Chondrocyte Implantation Versus Autologous Mosaicoplasty: a Randomized Trial chondrocytes Phase III: RCT, efficacy study transplantation; NCT00560664 Procedure: Mosaicoplasty Knee Osteoarthritis Not yet 156 Rec Knee Chondral or Osteochondral Defect Active, NR 76 293 Adt Jan-07 Dec-10 Hannover Sen Medical School http://ClinicalTrials.gov/show/NCT01185951 Adt Apr-12 Oct-14 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01410786 Adt May-11 Jun-14 University Sen Hospital, Geneva http://ClinicalTrials.gov/show/NCT01406652 Adt Aug-11 Sep-13 Madigan Army http://ClinicalTrials.gov/show/NCT01427153 Sen Medical Center; Brooke Army Medical Center; Wilford Hall Medical Center Adt Apr-07 Dec-12 University http://ClinicalTrials.gov/show/NCT00560664 Hospital, Brest; Institut National de la Santé Et de la Recherche Médicale, France Randomized Control Trial on Postoperative Weight Bearing After High Tibial Osteotomy (HTO) RCT, safety/efficacy study NCT00799370 Allogeneic Vascularized Knee Transplantation Single group assignment, safety/efficacy study NCT01133145 Procedure: Early Osteoarthritis, Knee weight bearing; Procedure: Delayed weight bearing Procedure: knee joint Osteitis; Limb transplantation Salvage; Joint Deformities, Acquired; Skin Transplantation; Bone Transplantation Evaluation of Optimal Dose of Procedure: PC-FNB Arthropathy of Knee Local Anesthetics for Patient with basal Joint Controlled Continuous Femoral administration of Nerve Block local anesthetics; RCT, efficacy study Procedure: PC-FNB NCT01198340 without basal local anesthetics Follow-up of Patients After Knee Procedure: History Knee Arthrodesis Arthrodesis With an Intramedullary taken and clinical With Intramedullary Nail examination Nail Single group assignment, efficacy study NCT00284297 Restricted vs. Free Knee Range Of Procedure: Locked Patellar Dislocation Motion For Primary Traumatic knee brace; Patellar Dislocation Procedure: Locked RCT knee brace NCT01344915 A Prospective Randomized Study Procedure: Patella-Dislocation; of Medial Patellofemoral Ligament Patellofemoral Patellofemoral (MPFL) Reconstruction stabilizing surgery Osteoarthritis; RCT Patellar Instability NCT00816647 Rec 136 Adt Nov-08 Nov-12 Hospices Civils de Lyon http://ClinicalTrials.gov/show/NCT00799370 Invite 6 Adt http://ClinicalTrials.gov/show/NCT01133145 Rec 60 Adt Sep-10 Jun-12 Okayama Sen University Rec 20 Adt Sep-05 Aug-11 University http://ClinicalTrials.gov/show/NCT00284297 Sen Hospital, Ghent Active, NR Term Jun-12 University of Jena Adt Dec-05 Jun-11 Tampere University Hospital 50 294 http://ClinicalTrials.gov/show/NCT01198340 http://ClinicalTrials.gov/show/NCT01344915 Adt Dec-08 Jun-11 Finnish Defense http://ClinicalTrials.gov/show/NCT00816647 Forces; Tampere University Hospital, Department of Musculosceletal Diseases Patellar Tendon Regeneration With Platelet-rich Plasma Phase IV: RCT, efficacy study NCT01111747 Procedure: Platelet- Knee Instability rich plasma; Procedure: Control group Active, NR 27 Hyperpronation and Foot-pains RCT, safety/efficacy study NCT00736138 Procedure: training and pellots Comp 50 Rec 72 Active, NR 20 Comp 43 Comp 40 Active, NR 76 Arthrosis in Knee Local Analgesia in Knee- and Procedure: Position Rheumatoid Arthritis; Hipatroplastic Surgery in Patients of catheter Orthopedic Surgery; With Rheumatic Disease: ExtraAnalgesia vs. Intracapsulare Position of Catheter RCT, efficacy study NCT01050738 Weightbearing After High Tibial Procedure: Unlimited Osteoarthritis, Knee Osteotomy postoperative Phase IV: RCT, efficacy study weightbearing NCT00426907 Outcome After Soft Tissue Procedure: Patella Dislocation Realignment of the Tibial Insertion Medialising insertion of the Patella Tendon of patella tendon Single group assignment, safety/efficacy study NCT01059721 Results of Opening-wedge High Procedure: Iliac crest Genovarum Tibial Osteotomy Using Iliac Crest allograft; Procedure: Allograft Compared to Iliac Crest Iliac crest autograft Autograft Phase III: RCT NCT00595712 Comparison of Autologous Procedure: Knee Chondral or Chondrocyte Implantation Versus Autologous Osteochondral Mosaicoplasty: a Randomized Trial chondrocytes Defect Phase III: RCT, efficacy study transplantation; NCT00560664 Procedure: Mosaicoplasty 295 Child Nov-08 Dec-10 University of Sao http://ClinicalTrials.gov/show/NCT01111747 Adt Paulo General Hospital; Instituto de Ortopedia e Traumatologia HCFMUSP São Paulo, Brazil Adt Jan-07 Dec-10 Northern http://ClinicalTrials.gov/show/NCT00736138 Sen Orthopaedic Division, Denmark Child Jan-10 Aug-10 Spenshult http://ClinicalTrials.gov/show/NCT01050738 Adt Hospital Sen Adt Jan-07 Aug-10 Northern Orthopaedic Division, Denmark Child Jan-10 Jul-10 Medical Adt University of Graz http://ClinicalTrials.gov/show/NCT00426907 Child Sep-07 Feb-10 Tehran Adt University of Medical Sciences http://ClinicalTrials.gov/show/NCT00595712 Adt http://ClinicalTrials.gov/show/NCT01059721 Apr-07 Dec-12 University http://ClinicalTrials.gov/show/NCT00560664 Hospital, Brest; Institut National de la Santé Et de la Recherche Médicale, France Oxford Partial Knee Comparative Instrument Pilot Study Non-randomized, parallel assignment NCT01410786 Optimisation of the Treatment of Infectious Bursitis Phase III: RCT, safety/efficacy study NCT01406652 Other Functional and Quality of Life Outcomes Following Viscosupplementation for Knee Osteoarthritis Prospective, case-only study NCT01447303 Shared Decision Making in Patients With Osteoarthritis of the Hip and Knee RCT NCT01492257 Structured Non-operative Treatment of Knee Osteoarthritis RCT, efficacy study NCT01535001 Procedure: Osteoarthritis, Knee Not yet 70 Conventional Rec Instrumentation; Procedure: Signature Custom Guides Procedure: TwoOlecranon Bursitis; Rec 240 stage bursectomy Patellar Bursitis Adt Apr-12 Oct-14 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT01410786 Adt May-11 Jun-14 University Sen Hospital, Geneva http://ClinicalTrials.gov/show/NCT01406652 Other: Subject Knee Osteoarthritis outcomes following viscosupplementatio n of the knee Rec 500 Adt Aug-09 Aug-15 University of Sen Florida http://ClinicalTrials.gov/show/NCT01447303 Other: Shared Decision Making Intervention Hip Osteoarthritis; Knee Osteoarthritis Rec 120 Adt Sen http://ClinicalTrials.gov/show/NCT01492257 Other: Neuromuscular training (NEMEXTJR); Behavioral: Information; Drug: Paracetamol; Drug: Burana; Drug: Pantoprazole; Behavioral: Dietary counseling; Behavioral: Patient education; Other: Insoles Osteoarthritis of the Knee Not yet 100 Rec 296 Jul-11 Jul-14 University of California, San Francisco; Stanford University; Robert Wood Johnson Foundation Adt Feb-12 Mar-14 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT01535001 Effectiveness of a Knee Brace When Combined With Viscosupplementation in the Treatment of Knee Osteoarthritis RCT, efficacy study NCT01478386 Rec 150 Adt Dec-11 Jan-14 OAD Sen Orthopaedics http://ClinicalTrials.gov/show/NCT01478386 Not yet Rec 70 Adt Jun-11 Sep-13 St. Michael's Sen Hospital, Toronto http://ClinicalTrials.gov/show/NCT01296750 Knee Osteoarthritis Rec 284 Adt Feb-12 Sep-13 Central Hospital, http://ClinicalTrials.gov/show/NCT01544647 Sen Nancy, France Knee Degenerative Disease; Knee Arthrosis; Knee Osteoarthritis; Osteoarthritis, Knee Rec 12 Adt May-10 Jun-13 Red de Terapia http://ClinicalTrials.gov/show/NCT01183728 Sen Celular, Spain Knee Osteoarthritis Rec 80 Active, NR 15 Adt Jun-09 Jun-13 University of Sen Zurich; Kantonsspital Olten; Kantonsspital Aarau; Lund University; Maastricht University Adult Jan-09 Aug-12 RTI Biologics Other: Orthovisc; Knee Osteoarthritis Device: DonJoy HA lite knee brace; Device: Orthovisc injections and DonJoy HA lite knee brace Other: Early Traumatic Knee Physiotherapy start Dislocation Late Compared to Early Physiotherapy Following Knee Dislocation Phase III: RCT NCT01296750 Spa Therapy in Knee Other: Usual spa Osteoarthritis (OA): Nancy-thermal protocol; Other: RCT, efficacy study Active spa protocol NCT01544647 Treatment of Knee Osteoarthritis Other: Autologous With Autologous Mesenchymal bone marrow Stem Cells mesenchymal stem Phase I/II: Single group cells (MSV) assignment, safety/efficacy study NCT01183728 Effect of Pre-surgery Other: preoperative Neuromuscular Physiotherapy neuromuscular (PT) training; Behavioral: Phase III: RCT, efficacy study knee OA School NCT00913575 Evaluation of the CR Plug for Other: CR Plug Repair of Defects Created at the Harvest Site From an Autograft in the Knee. Phase III: Single group assignment, efficacy study NCT00821873 Knee Injury 297 http://ClinicalTrials.gov/show/NCT00913575 http://ClinicalTrials.gov/show/NCT00821873 An Analysis of Potential Sex Other: Differences in Knee Osteoarthritis musculoskeletal Prospective, cohort study NCT01403207 Degenerative Joint Disease; Osteoarthritis Evaluation of the Composite of Other: Primary injury Knee Injury Cancellous and Demineralized site; Other: Backfill Bone Plug (CR-Plug) for Repair of site Osteochondral Defects in the Knee Phase III: RCT, safety/efficacy study NCT00984594 Comparing Manipulation, Other: Full Kinetic Osteoarthritis, Knee Rehabilitation and Combination of Chain Manipulative the Two in the Treatment of Knee Therapy; Other: Full Osteoarthritis Kinetic Chain RCT, safety/efficacy study Rehabilitation; Other: NCT01188837 Full Kinetic Chain Manipulative Therapy with Rehabilitation Moxibustion for Knee Other: Moxibustion Idiopathic Osteoarthritis treatment plus usual Osteoarthritis Phase I/II: RCT, safety/efficacy care; Other: Usual study care alone group NCT01354860 The Effects of Topical Calcium Other: Topical Wound Healing; Glycerophosphate on Surgical calcium Scarring Wound Healing and Residual glycerophosphate Scarring lotion RCT, efficacy study NCT01264588 Rec 20 Active, NR 20 Rec 144 Adt Sep-10 Oct-11 Cleveland http://ClinicalTrials.gov/show/NCT01188837 Sen Chiropractic College; Durban University of Technology South Africa; Murdoch University Comp 40 Adt Dec-10 May-11 Korea Institute of http://ClinicalTrials.gov/show/NCT01354860 Sen Oriental Medicine Comp 20 Adt Apr-08 Dec-10 AkPharma Inc.; http://ClinicalTrials.gov/show/NCT01264588 Sen Rothman Institute Orthopaedics; Texas Tech University Health Sciences Center; cyberDERM Clinical Studies; Bacharach Institute for Rehabilitation 298 Adt Aug-11 Jul-12 Mary O'Connor; http://ClinicalTrials.gov/show/NCT01403207 Sen Society of Women's Health Research; University of Calgary; Florida State University; Georgia Institute of Technology Adult Jan-09 May-12 RTI Biologics http://ClinicalTrials.gov/show/NCT00984594 Enhancing the Effectiveness of Physical Therapy for People With Knee Osteoarthritis Phase II/III: RCT, efficacy study NCT01314183 Effect of Mobilization on Acute Postoperative Pain and Nociceptive Function Phase IV: Prospective, cohort study NCT01018277 Osteoarthritis Not yet 300 Rec Adt Sen Other: Mobilization (walking) Pain, Postoperative; Pain Sensitivity, Postoperative Comp 26 Adt Dec-09 Jun-10 Hvidovre Sen University Hospital; Lundbeck Foundation http://ClinicalTrials.gov/show/NCT01018277 Joint Disease Wdrwn 0 Adt Dec-09 Jun-23 Sen http://ClinicalTrials.gov/show/NCT00754637 OA Knee Rec 5000 Adt Sep-01 Dec-20 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00261066 Sen Research Institute Pain; Arthritis Invite 200 Adt Mar-09 Dec-18 Sen Osteoarthritis, Knee; Rec Osteonecrosis 148 Adt Sen Healthy; Medial Patellofemoral Ligament Reconstruction 50 Adt May-10 May-15 Sen Miscellaneous observational studies Microplasty Tibial Tray Data Collection Prospective, cohort study NCT00754637 Outcome Following Orthopaedic Surgery Prospective, cohort study NCT00261066 Regenerex Tibial Tray Multi-Center Data Collection Prospective, cohort study NCT00859963 Treatment of Medial Compartmental Osteoarthritis Grade 1-4 (According to KellgrenLawrence) or Osteonecrosis With TomoFix™ Small or Conservatively Prospective, cohort study NCT01048710 Medial Patellofemoral Ligament Reconstruction: A Review of Technique, Accuracy, and Outcome Cross-sectional, cohort study NCT01405729 Invite 299 N/K Nov-10 Agency for http://ClinicalTrials.gov/show/NCT01314183 Healthcare Research and Quality (AHRQ) Other: Exercise; Other: manual therapy Jul-09 Feb-16 Biomet, Inc. Biomet, Inc. http://ClinicalTrials.gov/show/NCT00859963 AO Clinical http://ClinicalTrials.gov/show/NCT01048710 Investigation and Documentation; Synthes Inc. University of Utah http://ClinicalTrials.gov/show/NCT01405729 Creating a Tissue Bank of Knee Capsules Retrospective, cohort study NCT01320124 Osteoarthritis; Knee Rec Joint Contractures Monitoring of Acute Knee Injuries to Understand Osteoarthritis Development Prospective, case-only study NCT01382173 Chronic Knee Pain Study Cross-sectional, cohort study NCT00776932 Traumatic Knee Injury; Knee Osteoarthritis Knee Osteoarthritis Active, NR 522 Assessment of Blood Loss With a Point Of Care Device Prospective, cohort study NCT01430273 Acute Arthropathy of Rec Knee, Patella, Tibia, or Fibula 200 The Parapatellar Approach to Intramedullary Tibial Nailing Prospective, cohort study NCT01407718 Efficiency of Patellar Taping in Treatment of Patellofemoral Pain Syndrome Prospective, cohort study NCT01504100 Characterizing Knee Pain and Response to Surgery Using Local Biomarkers Prospective, case-only study NCT00961623 Validation of an Online Knee Pain Map and Questionnaire: A Probabilistic Diagnostic Tool Prospective, cohort study NCT01492244 Knee Pain Intermittent 60 Not yet Rec Active, NR 1500 Adt Mar-11 Dec-14 Ottawa Hospital http://ClinicalTrials.gov/show/NCT01320124 Sen Research Institute; Canadian Institutes of Health Research 600 Child Sep-11 Jan-14 Lund University http://ClinicalTrials.gov/show/NCT01382173 Adt Adt Jun-07 Jun-13 Sen University of http://ClinicalTrials.gov/show/NCT00776932 Pittsburgh; National Institutes of Health Adt Jul-11 Aug-12 Assistance http://ClinicalTrials.gov/show/NCT01430273 Sen Publique Hôpitaux de Paris; Ministry of Health, France Adt Jun-10 Jul-12 University of http://ClinicalTrials.gov/show/NCT01407718 Sen Utah Patellofemoral Pain Rec Syndrome 100 Adt May-11 May-12 National Taiwan http://ClinicalTrials.gov/show/NCT01504100 University Hospital Inflammation Rec 150 Adt Sen Knee Pain Rec 1000 Adt Dec-11 Dec-11 Sen 300 Jul-09 Dec-11 Stanford University http://ClinicalTrials.gov/show/NCT00961623 Brock Foster; TMT Medical Incorporated http://ClinicalTrials.gov/show/NCT01492244 The Effects of Bariatric Surgery Weight Loss on Knee Pain in Patients With Osteoarthritis of the Knee Prospective, case-only study NCT00752765 Evaluation of Ultrasonic Neuroma Size With Residual Limb Pain in Above-Knee Amputees Cross-sectional, case-only study NCT00686764 Knee Pain; Knee Osteoarthritis Rec 30 Adt Sep-08 Sep-10 Sen Penn State University http://ClinicalTrials.gov/show/NCT00752765 Neuroma Amputation Comp 7 Adt May-08 Feb-10 Oregon Health Sen and Science University Interventions Conditions Recruit n Drug: Botulinum Toxin (Type A) injection (10 U/Kg) Clubfoot Drug: Botox Idiopathic Clubfoot (Talipes Equinovarus) Active, NR 36 Child Sep-05 Feb-13 University of http://ClinicalTrials.gov/show/NCT00152347 British Columbia Drug: Botox Idiopathic Clubfoot (Talipes Equinovarus) Active, NR 50 Child Sep-05 Dec-12 University of http://ClinicalTrials.gov/show/NCT00152334 British Columbia http://ClinicalTrials.gov/show/NCT0068 6764 A10. FOOT AND ANKLE A10A: PAEDIATRICS Title Phases: trial design (control) CT ID Drugs including biologics Using Botox to Treat Patients With Idiopathic Clubfoot Single group assignment, efficacy study NCT00474032 A Double-Blind, Randomized Control Trial Comparing Botulinum Toxin Type A (Botox) and Placebo in the Treatment of Idiopathic Clubfoot RCT, efficacy study NCT00152347 Efficacy of Botox in Patients With Idiopathic Clubfoot Single group assignment, efficacy study NCT00152334 Rec Age Start (Grp) Date End Sponsors Date URL 2000 Child Mar-03 Mar-23 University of http://ClinicalTrials.gov/show/NCT00474032 British Columbia 301 Pharmacokinetic of levobupivacaïne After Sciatic Nerve Block in Children Phase III: Single group assignment, pharmacokinetics study NCT00682344 CLONidine and ROPivacaine in peripheral nerve blocks in children RCT, efficacy study ISRCTN90832436 Botox Clinical Trial Phase IV: RCT NCT00624299 Botulinum toxin: an adjunct in limb reconstruction - Can it reduce pain and joint complications in the lengthening phase? RCT ISRCTN35609758 Drug: Levobupivacaïne Surgical Pathology of the Leg or the Foot. Rec 27 Child Jan-08 Jul-12 Assistance Publique Hopitaux de Marseille Isotonic saline; Clonidine; Clonidine plus 0.2% Ropivacaine Drug: Botox; Other: Saline Disturbances of Achilles tendon and club foot Comp 77 Leg Length Inequality; Foot Deformities Limb reconstruction surgery; femoral or tibial deformity; congenital talipes equinovarus Not yet Rec 36 Comp 36 Child Jan-09 May-10 General http://www.controlledChildren's trials.com/ISRCTN90832436 Hospital (Greeece) Child Mar-08 May-10 Sheffield http://ClinicalTrials.gov/show/NCT00624299 Children's NHS Foundation Trust Child Apr-08 Apr-10 Sheffield http://www.controlledChildren's NHS trials.com/ISRCTN35609758 Foundation Trust (UK) Botulinum toxin intramuscular injections; Saline injections Miscellaneous observational studies Economic Evaluation of Clubfoot Treatment: One Centre's Experience Retrospective, case-only study NCT00475631 Pedobarographic Assessments of Clubfoot Treated Patients Prospective, cohort study NCT00175708 Outcomes of Compliance With Brace Wear in Clubfoot Prospective, case-only study NCT01481324 http://ClinicalTrials.gov/show/NCT00682344 Clubfoot Rec 600 Child Oct-03 Dec-23 University of http://ClinicalTrials.gov/show/NCT00475631 British Columbia Clubfoot Rec 100 Child Sep-05 Dec-11 University of http://ClinicalTrials.gov/show/NCT00175708 British Columbia Clubfoot Rec 70 302 Child Oct-09 Nov-11 Shriners http://ClinicalTrials.gov/show/NCT01481324 Hospitals for Children; Kosair Charities, Inc. A10B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Behavioural A trial comparing weight bearing to non-weight bearing following ankle fracture fixation RCT ISRCTN33416471 Early Weightbearing and Mobilization Versus NonWeightbearing and Mobilization in Unstable Ankle Fractures RCT, efficacy study NCT01196338 Device Tightrope or Screw Fixation of Acute Tibiofibular Syndesmotic Injury RCT, efficacy study NCT01275924 Foot and Ankle Range of Motion (Stretching) Apparatus RCT, efficacy study NCT00527748 Foot and Ankle Range of Motion (Stretching) Apparatus RCT, efficacy study NCT00527748 Interventions Conditions Weight-bearing; non- Closed ankle weight-bearing fractures Behavioral: Early weight-bearing and range of motion exercises; Behavioral: nonweight bearing, no range of motion Ankle Injuries Recruit n Active 76 Age Start (Grp) Date End Sponsors Date URL Adt Jan-11 Dec-13 St George's http://www.controlledSen Healthcare NHS trials.com/ISRCTN33416471 Trust (UK) Rec 110 Child Sep-10 Jun-12 University of Adt Toronto; Sen Orthopaedic Trauma Association; Canadian Orthopaedic Foundation; Künzli SwissSchuh Device: Tightrope Syndesmotic Injury Syndesmosis Repair of the Ankle Kit; Device: Syndesmotic screw Rec 100 Adt Jan-11 Dec-14 Sykehuset Asker http://ClinicalTrials.gov/show/NCT01275924 Sen og Baerum; Oslo University Hospital Device: NonMeasuring Ankle Exerciser (Ankle Recovery Mechanism) Device: NonMeasuring Ankle Exerciser (Ankle Recovery Mechanism) Plantar Fasciitis; Flatfoot; Calcaneus Fractures Rec 100 Adt Sep-07 Sep-13 University of Sen MissouriColumbia http://ClinicalTrials.gov/show/NCT00527748 Plantar Fasciitis; Flatfoot; Calcaneus Fractures Rec 100 Adt Sep-07 Sep-13 University of Sen MissouriColumbia http://ClinicalTrials.gov/show/NCT00527748 303 http://ClinicalTrials.gov/show/NCT01196338 Prospective Study on Artelon® Device: Artelon Tissue Reinforcement in Repair of Chronic Ruptures and Re-ruptures of the Achilles Tendon Single group assignment NCT01237613 Compression Treatment Effects on Device: Intermittent Complications and Healing of pneumatic Achilles Tendon Rupture compression RCT, efficacy study (VenaFlow Elite NCT01317160 system) A Multicenter Randomized Trial Comparing Antiglide and Lateral Plate Fixation in Ankle Fractures RCT, bio-equivalence study NCT00718302 Lateral Ankle Sprain Study RCT NCT00761865 A Double Blind Randomized Study on Adjunctive Use of Pulsed Electromagnetic Fields in the Treatment of 5th Metatarsal NonUnion Fracture RCT, efficacy study NCT00586170 Comparison of Biodegradable & Metal Plates for Fixing Ankle Fracture Safety/efficacy study NCT00864877 Bi-trimalleolar Fracture and APOS System Treatment Phase I: RCT NCT01127776 Tape versus brace treatment of ankle distortion RCT, efficacy study ISRCTN58932628 Achilles Tendon Rupture Rec 10 Adt Nov-10 Jul-13 Orthopedic Foot http://ClinicalTrials.gov/show/NCT01237613 Sen and Ankle Center, Ohio; Artimplant AB Rupture; Venous Thromboembolism; Venous Thrombosis; Surgical Wound Infection Rec 100 Active, NR 249 Adt Mar-11 Jun-13 Karolinska http://ClinicalTrials.gov/show/NCT01317160 Sen University Hospital; Stockholm County Council, Sweden; DJO Incorporated Adt Jun-08 Dec-12 Boston Medical http://ClinicalTrials.gov/show/NCT00718302 Sen Center Rec 100 Term 9 Device: Antiglide Ankle Injuries Plate; Device: Lateral Plate Device: Air Cast Later Ankle Sprain Stirrup Brace & High Tide Fracture Boot Device: EBI Bone 5th Metatarsal Non Healing System Union Fracture Adt Oct-08 Aug-12 University of Sen Rochester Adt Nov-07 Aug-12 EBI, LLC dba http://ClinicalTrials.gov/show/NCT00586170 Sen Biomet Spine, Biomet Trauma, Biomet Osteobiologics and Biomet Bracing Adt May-09 Apr-12 Inion Oy http://ClinicalTrials.gov/show/NCT00864877 Device: Distal Fibular Not yet biodegradable Fracture; Bimalleolar Rec fixation system (Inion Fracture; OTPS Trimalleolar Fracture FreedomPlateTM) Device: APOS Bi-trimalleolar Rec 60 Adult Oct-10 Mar-12 Meir Medical SYSTEM; Other: Fracture of Ankle Center APOS SYSTEM without biomechanics units. Tape treatment; Ankle distortion, Comp 100 Child Jan-08 Dec-11 Maastricht semi-rigid brace ankle ligament Adt University (AirLoc® Bauerfeind, rupture Medical Center Germany) (Netherlands) 304 http://ClinicalTrials.gov/show/NCT00761865 http://ClinicalTrials.gov/show/NCT01127776 http://www.controlledtrials.com/ISRCTN58932628 Tape Versus Semirigid Versus Lace-up Ankle Support in the Treatment of Acute Lateral Ankle Ligament Injury. Phase IV: RCT, safety/efficacy study NCT01126242 Outcomes of Operative Treatment of Unstable Ankle Fracture Comparison Between Metallic and Biodegradable Implants Phase IV: RCT, efficacy study NCT01431560 A Comparison of Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries Phase IV: RCT NCT00689962 Acute Achilles Repair With or Without OrthADAPT Augmentation RCT, efficacy study NCT00962143 Device: Tape; Grade II and III Device: Semi rigid Acute Lateral Ankle brace; Device: Lace- Ligament Injuries up brace Device: fixation of Ankle Fracture the ankle fracture (Solco ); Device: fixation of the ankle fracture (Freedom) Comp Device: Linvatec 4.5 Joint Instability mm Smart Screw; Device: Synthes 4.0 mm steel screw Device: Achilles repair with OrthADAPT augmentation; Procedure: Achilles repair without OrthADAPT Augmentation Achilles Tendon Tear Dietary supplement The Effect of Vitamin c on Dietary Supplement: Ankle Fracture Preventing Complex Regional Pain vitamin c; Drug: Syndrome (CRPS Type I) placebo Following Ankle Fracture RCT, efficacy study NCT01338129 Drugs including biologics The Use of Teriparatide as an Adjunctive Therapy for the Treatment of Jones Fractures Phase IV: RCT, efficacy study NCT01173081 Rec Drug: Teriparatide; Drug: Placebo Fractures 182 Adt May-10 Nov-11 Gelre Hospitals http://ClinicalTrials.gov/show/NCT01126242 Sen 109 Child Jun-08 Aug-11 National Police Adt Hospital Sen http://ClinicalTrials.gov/show/NCT01431560 Rec 60 Adt Sen http://ClinicalTrials.gov/show/NCT00689962 Term 55 Adt Jun-08 Jan-11 Synovis Surgical http://ClinicalTrials.gov/show/NCT00962143 Sen Innovations Not yet 100 Rec Rec 38 305 Jul-08 Jul-11 Rothman Institute Orthopaedics Adt Apr-11 Feb-14 Rabin Medical Sen Center Adt Sen http://ClinicalTrials.gov/show/NCT01338129 Jul-10 Apr-14 Ohio Orthopedic http://ClinicalTrials.gov/show/NCT01173081 Center of Excellence; Eli Lilly and Company Low-Molecular-Weight Heparin (LMWH) for Deep Venous Thrombosis (DVT) Prophylaxis Non-randomized, parallel assignment, safety/efficacy study NCT01029821 Lymphomyosot for Ankle Edema Following Fracture Phase II: RCT, safety/efficacy study NCT00884988 Platelet rich plasma in Accelerated Tendo-achilles Healing RCT, efficacy study ISRCTN93608625 Drug: LowMolecular-Weight Heparin Deep Venous Thrombosis; Ankle fractures Rec 100 Adt Feb-10 Dec-13 University of Sen Tennessee http://ClinicalTrials.gov/show/NCT01029821 Drug: Lymphomyosot; Drug: Placebo remedy Ankle Injuries; Fracture Susp 60 Adt Feb-10 Dec-12 Shaare Zedek Sen Medical Center http://ClinicalTrials.gov/show/NCT00884988 Standard cast immobilisation group ± Platelet rich plasma; Standard surgical repair ± Platelet rich plasma Drug: Nadroparin; Drug: Fondaparinux Acute achilles tendon rupture Active 360 Adt Nov-09 Nov-12 University of Oxford (UK) http://www.controlledtrials.com/ISRCTN93608625 Rec 669 Adt Apr-09 Apr-11 Red Cross Sen Hospital Beverwijk http://ClinicalTrials.gov/show/NCT00881088 Rec 669 Adt Apr-09 Apr-11 Red Cross Sen Hospital Beverwijk http://ClinicalTrials.gov/show/NCT00881088 Prophylaxis of Thromboembolic Deep Vein Complications Trial: Thrombosis; Thromboprophylaxis Needed in Pulmonary Below Knee Plaster Cast Embolism Immobilization for Ankle and Foot Fractures Phase II/III: RCT, safety/efficacy study NCT00881088 Prophylaxis of Thromboembolic Drug: Nadroparin; Deep Vein Complications Trial: Drug: Fondaparinux Thrombosis; Thromboprophylaxis Needed in Pulmonary Below Knee Plaster Cast Embolism Immobilization for Ankle and Foot Fractures Phase II/III: RCT, safety/efficacy study NCT00881088 306 Procedure Combined Randomised and Observational Study of Type B Ankle Fracture Treatment RCT, safety/efficacy study NCT01134094 Procedure: Open Ankle Fractures reduction internal fixation of the ankle; Procedure: Non Operative Arthrodesis Versus Extra-articular Procedure: Lisfranc Injuries Platefixation in Lisfranc Injury Temporary RCT, efficacy study extraarticular plate NCT01448941 fixation Comparison of close contact cast Close contact casting Displaced unstable (CCC) technique to open surgical technique; Open fracture of the ankle reduction and internal fixation surgical reduction + (ORIF) in the treatment of unstable internal fixation ankle fractures in patients over 60 years RCT ISRCTN04180738 Hyperbaric Oxygen Therapy in Procedure: HBOT; Microcirculation; Calcaneal Intraarticular Fractures: Procedure: Placebo Wound Healing Can it Decrease the Soft-tissue (Sham) Complication Rate? RCT, safety/efficacy study NCT01264146 Non-operative Treatment of Acute Procedure: Early Acute Achilles Achilles Tendon Rupture Using weight-bearing Tendon Rupture Dynamic Rehabilitation. Influence of Early Weight-bearing Compared With Non-weight-bearing RCT, efficacy study NCT01470833 Aspiration for Pain Relief Following Procedure: Ankle Ankle Fracture Ankle Fracture Aspiration; RCT, safety/efficacy study Procedure: Ankle NCT01484535 aspiration Standard Anterolateral Rec 160 Rec 50 Active 620 Adt Oct-09 Oct-14 University of Sen Oxford (UK) http://www.controlledtrials.com/ISRCTN04180738 Rec 160 Adt Jan-11 Jul-14 RWTH Aachen Sen University http://ClinicalTrials.gov/show/NCT01264146 Rec 60 Adt http://ClinicalTrials.gov/show/NCT01470833 Invite 120 Adt Sep-11 Dec-13 Mayo Clinic Sen 307 Adt Aug-10 Dec-16 The University of http://ClinicalTrials.gov/show/NCT01134094 New South Wales; Whitlam Orthopaedic Research Centre; CROSSBAT Investigators Adt Oct-11 Dec-15 Oslo University http://ClinicalTrials.gov/show/NCT01448941 Hospital Apr-11 Apr-14 Hvidovre University Hospital; DJO Incorporated http://ClinicalTrials.gov/show/NCT01484535 Comparative Study of Fixation or Fusion of Calcaneal Fractures RCT NCT00679393 Procedure: Open reduction internal fixation; Procedure: Fusion Fractures, Comminuted; Fracture Fixation, Internal Closed Reduction versus Open reduction and internal fixation versus Non-Operative Study of intra-articular calcaneal fractures RCT ISRCTN67665340 Vacuum Assisted Closure as a Treatment for Soft Tissue Injuries RCT, efficacy study NCT00582998 Vacuum Assisted Closure as a Treatment for Soft Tissue Injuries RCT, efficacy study NCT00582998 Identification of Microcirculation After Surgical Treatment of Rupture of the Achilles Tendon Prospective, case-only study NCT01265004 A Comparison of Stainless Steel and Bioabsorbable Screw Fixation of Lisfranc Foot Injuries Phase IV: RCT NCT00985023 Closed reduction; open reduction + internal fixation; conservation treatment Intraarticular calcaneal fractures Active Procedure: Standard Fracture of Wound Dressing; Calcaneus, Pilon or Device: VAC Tibial Plateau Active, NR 189 Procedure: Standard Fracture of Wound Dressing; Calcaneus, Pilon or Device: VAC Tibial Plateau Active, NR 189 Microcirculation; Achilles Tendon Rupture Rec 90 Unstable Lisfranc Fracture-dislocations of the Midfoot Rec 60 Adt Aug-08 Aug-12 Rothman Sen Institute Orthopaedics http://ClinicalTrials.gov/show/NCT00985023 Comp 20 Adt Feb-10 Feb-12 University of Sen Warwick (UK) http://www.controlledtrials.com/ISRCTN95369715 Procedure: Stitches; Procedure: Fibringlue; Procedure: Stitches and Fibringlue Procedure: Steel screw fixation of Lisfranc fracturedislocation.; Procedure: Absorbable screw fixation of Lisfranc fracture-dislocations. Achilles Tendinopathy Plasma-rich plasma; Management: platelet-rich plasma Eccentric loading versus eccentric loading programme. programme RCT Achilles tendinopathy Rec 66 Child Feb-04 Dec-13 University of http://ClinicalTrials.gov/show/NCT00679393 Adt Calgary; Orthopaedic Trauma Association; AO North America 150 Adt Jul-06 Jul-13 Erasmus http://www.controlledSen Medical Center, trials.com/ISRCTN67665340 Department of Surgery (The Netherlands) ISRCTN95369715 308 Adt Jun-01 Dec-12 University of http://ClinicalTrials.gov/show/NCT00582998 Sen Alabama at Birmingham; KCI USA, Inc. Adt Jun-01 Dec-12 University of http://ClinicalTrials.gov/show/NCT00582998 Sen Alabama at Birmingham; KCI USA, Inc. Adt Dec-10 Dec-12 RWTH Aachen http://ClinicalTrials.gov/show/NCT01265004 Sen University Static Implant Versus Dynamic Implant in the Surgical Treatment on Ankle Syndesmosis Rupture RCT, efficacy study NCT01109303 Procedure: TightRope SystemArthrex® / Dynamic Implant; Procedure: Screw fixation Synthes® / Static Implant UK heel fracture trial: surgical Open reduction + treatment versus non-operative internal fixation; care conservation with RCT elevation + ice + ISRCTN37188541 spintage + early mobilisation Syndesmotic Injury and Fixation in Procedure: fixation Supination-External (SE) Ankle Fractures RCT, safety/efficacy study NCT01234493 Operative Versus Non Operative Procedure: non Treatment for Unstable Ankle operative treatment; Fractures Procedure: operative RCT vs non operative NCT00336752 treatment Open Reduction Internal Fixation Procedure: ORIF of of Calcaneus Fractures With and Calcaneus with bone Without Bone Graft grafting; Procedure: RCT, efficacy study ORIF of Calcaneus NCT00582686 without bone grafting AS04 Ankle study of fracture Surgical open treatment in the older patient reduction & internal RCT fixation (metal plates ISRCTN81174170 and screws); closed manipulation of the fracture & close contact cast. Trauma Expectation Factor Procedure: ankle or Trauma Outcome Measure distal tibia surgery Prospective, case-only study NCT01126398 Ankle Syndesmosis Rupture Active, NR 70 Closed displaced intra-articular fractures of the calcaneus Comop 150 Trauma Comp 140 Child Jun-07 Aug-10 University of Adt Oulu Sen http://ClinicalTrials.gov/show/NCT01234493 Ankle Injuries Comp 80 Adt http://ClinicalTrials.gov/show/NCT00336752 Calcaneus Fractures Active, NR 49 Adt May-00 Aug-10 University of Sen Alabama at Birmingham Unstable ankle fracture Comp 120 Adt May-04 Jul-10 Oxford Radcliffe http://www.controlledSen Hospitals NHS trials.com/ISRCTN81174170 Trust (UK) Ankle Fracture; Pilon Comp Fracture 204 Adt Feb-07 Feb-10 AO Clinical http://ClinicalTrials.gov/show/NCT01126398 Sen Investigation and Documentation 309 Adt Oct-08 Jan-12 Hopital de l'Enfant-Jesus; Arthrex, Inc. http://ClinicalTrials.gov/show/NCT01109303 Adt Jun-06 Nov-10 University http://www.controlledSen Hospitals trials.com/ISRCTN37188541 Coventry and Warwickshire NHS Trust (UK) Jun-03 Aug-10 Lawson Health Research Institute http://ClinicalTrials.gov/show/NCT00582686 Rest Easy: Is Bed Rest Really Necessary After Surgical Repair of an Ankle Fracture? RCT, safety/efficacy study NCT00690651 Other Alcohol Intervention in an Acute Surgical Setting RCT, efficacy study NCT00986791 Ankle Fracture Treatment in the Elderly Retrospective, case-only study NCT01444144 Ankle Sprain Rehabilitation With the Wii Balance Board RCT, safety/efficacy study NCT01449760 Ankle Manual Therapy for Ankle Sprains Phase II/III: RCT, safety/efficacy study NCT00888498 Procedure: Early Ankle Injuries; mobilization; Fracture Procedure: Standard mobilization Comp 104 Adt Sen Other: Postoperative Acute Surgery; alcohol cessation Alcohol Intervention; intervention Postoperative programme; Other: Morbidity; Infection; Standard treatment Ankle Injuries Other: Fracture union Ankle Fracture Rec 160 Adt Nov-09 Dec-15 Bispebjerg Sen Hospital, Denmark http://ClinicalTrials.gov/show/NCT00986791 Rec 150 Adt Mar-11 Mar-13 University of Sen Florida http://ClinicalTrials.gov/show/NCT01444144 Other: Physical Ankle Sprain Therapy; Other: Wii Balance Board Rec 300 Adt Mar-10 Mar-13 University Hospital, Geneva http://ClinicalTrials.gov/show/NCT01449760 Other: Passive Sprains and Strains Positioning; Other: High-Velocity, LowAmplitude Stretch; Other: Slow, Mobilization Stretch Rec 189 Child Jan-09 Dec-12 University of the http://ClinicalTrials.gov/show/NCT00888498 Adt Pacific; University of Southern California; American Physical Therapy Association 50 Child Jun-10 Dec-11 Rhode Island http://ClinicalTrials.gov/show/NCT01341015 Adt Hospital Bedside Ultrasound in the Other: Ultrasound Ankle Fracture Diagnosis of Ankle Fractures in Children Single group assignment, efficacy study NCT01341015 A Comparison of Early Mobilization Other: Jump Stretch Acute; Ankle; Sprain Versus Traditional Treatment for Acute Ankle Sprains. RCT NCT01134653 Rec Rec 60 310 Jul-08 Jan-10 The Alfred; http://ClinicalTrials.gov/show/NCT00690651 National Trauma Research Institute Child Jan-10 Jun-11 Nationwide Adt Children's Hospital http://ClinicalTrials.gov/show/NCT01134653 Miscellaneous observational studies Comparative Results of Conservatively and Surgically Treated Adolescents With Triplane and Juvenile Tillaux Ankle Fractures After Skeletal Maturity Prospective, cohort study NCT00541580 Intraoperative Three Dimensional Fluoroscopy Compared to Standard Fluoroscopy for the Assessment of Reduction of Ankle Fractures With Syndesmosis Disruption Prospective, cohort study NCT00556010 Adt Sep-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00541580 Adt Jan-09 Jul-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00556010 Ankle Injuries Term Ankle Injuries Active, NR 40 Conditions Recruit n Ankle Arthritis Rec 200 Adt Jun-02 Jan-10 St. Michael's Sen Hospital, Toronto; Johnson & Johnson Primary Arthrosis; Post Traumatic Arthritis; Rheumatoid Arthritis; Osteoarthritis Rec 98 Adt Nov-10 Jun-14 Small Bone http://ClinicalTrials.gov/show/NCT01284283 Sen Innovations, Inc. A10C: ARTHROPLASTY Title Interventions Phases: trial design (control) CT ID Behavioural Gait Analysis of Ankle Arthroplasty Behavioral: Gait and Arthrodesis Analysis Phase IV: Single group assignment NCT00921076 Device 2-Year Post-Approval Study to Investigate the Scandinavian Total Ankle Replacement System (STAR) Ankle Under Actual Conditions of Use Single group assignment, efficacy study NCT01284283 Device: Scandinavian Total Ankle Replacement System (STAR Ankle) 311 Age Start (Grp) Date End Sponsors Date URL http://ClinicalTrials.gov/show/NCT00921076 Post-Approval Study to Investigate the Long Term (8 Year) Survivorship of STAR Ankle Among Continued Access Study Patients Prospective, case control study NCT01288586 A Study to Evaluate the Effectiveness and Safety of an Implant in the Treatment of Osteoarthritis of the Great Toe Phase III: RCT NCT00969969 A randomised trial of ankle joint replacements RCT ISRCTN66721986 Drugs including biologics Evaluation of Trinity Evolution in Patients Undergoing Foot and Ankle Fusion Single group assignment NCT00988338 ACP for Local Application in Ankle Arthrodesis Non-randomized, parallel assignment NCT01131455 Device: Primary Arthrosis Scandinavian Total Ankle Replacement System (STAR Ankle) Rec 125 Adt Jan-11 May-14 Small Bone http://ClinicalTrials.gov/show/NCT01288586 Sen Innovations, Inc. Device: Arthrodesis; First MTP Joint Device: Cartiva Osteoarthritis Rec 230 Adt Aug-09 Aug-11 Carticept Sen Medical, Inc http://ClinicalTrials.gov/show/NCT00969969 Comp N/K N/K Jan-00 Jan-10 Department of Health (UK) http://www.controlledtrials.com/ISRCTN66721986 Tibiotalar Active, Arthrodesis; Subtalar NR Arthrodesis; Calcaneocuboid Arthrodesis; Talonavicular Arthrodesis; Double Arthrodesis (i.e. Calcaneocuboid and Talonavicular); Triple Arthrodesis (i.e. Subtalar, Calcaneocuboid, and Talonavicular) Ankle Arthritis Term 100 Adt Sep-09 Aug-12 Orthofix Inc. Sen http://ClinicalTrials.gov/show/NCT00988338 10 Adt Oct-09 Jul-10 Columbia Sen Orthopaedic Group, LLP http://ClinicalTrials.gov/show/NCT01131455 Scandinavian Total Total Ankle Ankle Replacement replacement (STAR); BuechelPappas (BP) total ankle replacements Biological: Trinity Evolution Biological: Autologous Concentrated Plasma 312 Procedure Canadian Orthopaedic Foot and Ankle Society Surgical Treatment of Ankle Arthritis Outcome Study Phase IV: RCT NCT00552136 Procedure: Ankle Arthroplasty; Procedure: Ankle Arthrodesis Total Ankle Replacement Versus Ankle Arthrodesis Trial RCT, efficacy study NCT01518361 Procedure: Total End-stage Ankle Ankle Replacement; Osteoarthritis Procedure: Ankle Arthrodesis Ankle Arthritis Rec Not yet 188 Rec Study of Subtalar Arthrodesis Using AlloStem® Versus Autologous Bone Graft RCT, safety/efficacy study NCT01413061 Procedure: Subtalar Degenerative Active, Arthrodesis Osteoarthritis; PostNR traumatic; Arthrosis; Rheumatoid Arthritis and Other Inflammatory Polyarthropathies; Rheumatoid Arthritis of Subtalar Joint Efficacy of a physical therapy Usual care + Ankle sprain Comp intervention for the early treatment standardised of acute ankle sprains identified in physical therapy the emergency department: a intervention; Usual randomised controlled trial care RCT ISRCTN74033088 Miscellaneous observational studies INBONE Total Ankle Arthroplasty(TAA)Using Calcaneal Stem Fixation Retrospective, case-only study NCT01366989 Arthrodesis; Degenerative Arthritis; Rheumatoid Arthritis; Complications; Arthroplasty, Mechanical Rec 136 Adt Feb-05 Apr-20 Capital District http://ClinicalTrials.gov/show/NCT00552136 Sen Health Authority, Canada; Canadian Orthopaedic Foot and Ankle Society; Johnson & Johnson Adt May-12 Jul-15 Razi Zaidi; http://ClinicalTrials.gov/show/NCT01518361 Sen University College, London; Medical Research Council Adt Jun-10 Dec-14 AlloSource http://ClinicalTrials.gov/show/NCT01413061 Sen 512 Child Sep-09 Aug-11 Queen’s Adt University Sen (Canada) 95 313 http://www.controlledtrials.com/ISRCTN74033088 Adt Oct-10 Dec-13 Wright Medical http://ClinicalTrials.gov/show/NCT01366989 Sen Technology; Duke University Short Term Follow-up of Patient Implanted With the MetatarsoPhalangeal Prosthesis METIS® Prospective, cohort study NCT01284985 Short Term Follow-up of Patient Implanted With the Proximal Interphalangeal Implant Prospective, cohort study NCT01285011 Follow-up of Patient Implanted With the Staple ASTUS® Prospective, case-only study NCT01518543 Agility LP Ankle Arthroplasty Outcomes Retrospective, case-only study NCT01366872 Arthroscopic Ankle Arthrodesis: Measuring Post-operative Pain to Assess the Potential for Outpatient Surgery. Prospective, case control study NCT01370252 Clinical Experience With the Hindfoot Arthrodesis Nail for the Surgical Treatment of Ankle and Hindfoot Pathologies Retrospective, case-only study NCT00942032 HINTEGRA Total Ankle Prosthesis Follow-up Case-only study NCT01284972 Hallux Rigidus; Active, Hallux Limitus; NR Hallux Valgus; Osteoarthritis; Rheumatoid Arthritis - Ankle and/or Foot Hammer Toe; Claw Active, Toe; Shortening 2nd NR Toe; Revision of Arthrodesis or Arthroplasty Failure Arthrodesis Term 115 Adt Feb-09 Jun-13 Integra Sen LifeSciences Services http://ClinicalTrials.gov/show/NCT01284985 153 Adt Apr-09 Jul-12 Integra Sen LifeSciences Services http://ClinicalTrials.gov/show/NCT01285011 5 Adt Apr-10 Mar-12 Integra Sen LifeSciences Services http://ClinicalTrials.gov/show/NCT01518543 Rheumatoid Arthritis of Ankle; Osteoarthritis of Ankle; Traumatic Arthritis of Ankle Osteoarthritis Rec 50 Adt Dec-10 Dec-11 Orthopaedic Sen Associates of Michigan, PC http://ClinicalTrials.gov/show/NCT01366872 Rec 40 Child Jun-11 Jun-11 Hammond, Adt Allan, M.D. Sen http://ClinicalTrials.gov/show/NCT01370252 Hindfoot Arthrodesis; Comp Hindfoot Pathologies 39 Child May-09 Apr-11 AO Clinical http://ClinicalTrials.gov/show/NCT00942032 Adt Investigation and Sen Documentation; Synthes Inc. Total Ankle Prosthesis 225 Adt Feb-09 Dec-10 Integra Sen LifeSciences Services Comp 314 http://ClinicalTrials.gov/show/NCT01284972 A10D: OTHER Title Phases: trial design (control) CT ID Device Augment™ Injectable Bone Graft Compared to Autologous Bone Graft as a Bone Regeneration Device in Hindfoot Fusions Phase III: RCT, safety/efficacy study NCT01305356 Comparison Between Implanted Functional Electrical Stimulation and Foot Orthosis RCT NCT01415700 Measures of Gait Efficiency of Three Multi-Axial, Vertical Shock and Energy Storing-Return Prosthetic Feet During Simple & Complex Mobility Activities RCT, safety/efficacy study NCT01404559 Evaluation of a Pro-Active Dynamic Accommodating Socket Cross-sectional, case-only study NCT01546311 Interventions Ankle Joint Replacement Outcomes Study Phase IV: Single group assignment, efficacy study NCT00503438 Device: ankle joint replacement Conditions Recruit n Device: Augment(tm) Degenerative Joint Injectable Bone Disease; Congenital Graft; Procedure: Deformity; Arthritis; Autologous bone Osteoarthritis; graft Rheumatoid Arthritis Rec 201 Adt Mar-11 Mar-14 BioMimetic Sen Therapeutics http://ClinicalTrials.gov/show/NCT01305356 Device: Functional Hysterical Simulation electrical stimulator; of Disease Device: feet orthosis Rec 50 Adt Oct-10 Jan-14 Assistance Sen Publique Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT01415700 Not yet Rec 28 Adt http://ClinicalTrials.gov/show/NCT01404559 Rec 5 Rec 200 Adt Jan-12 Dec-12 Infoscitex http://ClinicalTrials.gov/show/NCT01546311 Sen Corporation; Liberating Technologies, Inc; Telemedicine and Advanced Technology Research Center (TATRC) Adt Jul-07 Jun-12 Tornier http://ClinicalTrials.gov/show/NCT00503438 Sen Device: Ossur Amputation Ceterus prosthetic foot; Device: Ossur Variflex prosthetic foot; Device: Freedom Innovations Silhouette VS Device: Pro Active Amputation Dynamic Accommodating Socket Osteoarthritis; Rheumatoid Arthritis; Post-Traumatic Arthritis; Septic Arthritis; Prior Ankle Fusion 315 Age Start (Grp) Date End Sponsors Date Oct-11 Sep-13 University of South Florida URL A Study Evaluating Amplex Compared To Autograft Bone In Foot and Ankle Fusion Surgery Phase I/II: RCT, safety/efficacy study NCT01224119 Heel Cushion for Plantar Fasciitis Phase III: RCT, efficacy study NCT01017406 Device: Amplex; Arthritis Procedure: Autograft bone Device: PSU heel cushion and plantar fascia specific stretching exercise Comparative Study of Device: Fracture Osteosynthesis for Chevron compressing screw Osteotomy of Hallux Valgus Using ZfW 102 Königsee Degradable Versus NonImplantate GmbH; degradable Metallic Device Device: Fracture RCT, efficacy study compressing screw NCT01535144 titanium Königsee Implantate GmbH Comparative Study of Device: Fracture Osteosynthesis for Chevron compressing screw Osteotomy of Hallux Valgus Using ZfW 102 Königsee Degradable Versus NonImplantate GmbH; degradable Metallic Device Device: Fracture RCT, efficacy study compressing screw NCT01535144 titanium Königsee Implantate GmbH PISCES: Pressure and pain In Pressure relieving SCleroderma an Evaluation of a insole; Placebo Simple intervention insole RCT ISRCTN02824122 Artelon Metatarsophalangeal Device: Artelon MTP (MTP) Spacer Spacer Phase IV: Single group assignment NCT01028469 Augment™ Injectable Bone Graft Device: Augment™ Compared to Autologous Bone Injectable; Graft in Foot and Ankle Fusions Procedure: Standard RCT, safety/efficacy study of care NCT01008891 Active, NR 24 Adt Jan-11 Apr-12 BioSurface Sen Engineering Technologies, Inc http://ClinicalTrials.gov/show/NCT01224119 Plantar Fasciitis Invite 160 Child Jan-10 Apr-12 Prince of Adt Songkla University http://ClinicalTrials.gov/show/NCT01017406 Hallux Valgus Comp 26 Adt Feb-10 Feb-12 Syntellix AG Sen http://ClinicalTrials.gov/show/NCT01535144 Hallux Valgus Comp 26 Adt Feb-10 Feb-12 Syntellix AG Sen http://ClinicalTrials.gov/show/NCT01535144 Scleroderma Comp 140 Adt Sen http://www.controlledtrials.com/ISRCTN02824122 Rec 15 Child Dec-09 Dec-11 Artimplant AB Adt Sen http://ClinicalTrials.gov/show/NCT01028469 Active, NR 180 Adt Sep-09 Sep-11 BioMimetic Sen Therapeutics http://ClinicalTrials.gov/show/NCT01008891 Osteoarthritis; Hallux Rigidus Ankle/Hindfoot Fusion 316 Jul-10 Dec-11 University of Leeds (UK) Wdrwn 90 Adt Jun-07 Jul-11 ArthroCare Corporation http://ClinicalTrials.gov/show/NCT00420875 Term 60 http://ClinicalTrials.gov/show/NCT00949897 Amputation Active, NR 20 Orthopedic Surgery Not yet Rec 75 Functional foot Foot pain; Healthy orthoses; Inert cushioning orthoses Comp 120 Adt Mar-09 Jun-11 OrthoCarolina Sen Research Institute, Inc.; Wright Medical Technology Adt Mar-09 Jun-11 Department of Veterans Affairs; Massachusetts Institute of Technology Adt Feb-10 Apr-11 Nottingham Sen University Hospitals NHS Trust Adt May-09 Jan-11 University of Sen Leeds (UK) Device: Iceman® Narcotic Cold Therapy unit Consumption; Pain; (djOrtho); Other: Ice Wound Healing; Patient Satisfaction Term 82 Child Feb-07 Dec-10 OrthoCarolina Adt Research Sen Institute, Inc.; DJO Incorporated http://ClinicalTrials.gov/show/NCT00950183 Device: V.A.C. by K.C.I. Comp 106 Adt Aug-08 Oct-10 Georgetown Sen University http://ClinicalTrials.gov/show/NCT01366105 Comp 69 Adt Oct-09 Sep-10 Henry DeGroot, http://ClinicalTrials.gov/show/NCT01243814 Sen M.D. Clinical Evaluation of Placement of Device: TOPAZ Radiofrequency-based Plasma MicroDebrider Microdebridement in the Treatment Algorithm for Foot and Ankle Tendinosis and Plantar Fasciosis Phase IV: Single group assignment, efficacy study NCT00420875 Comparison Study of Biofoam Device: Biofoam; Porous Metal Versus Allograft to Other: Iliac Crest Treat Adult Acquired Flatfoot Allograft with locked Phase IV: RCT, efficacy study plate NCT00949897 Effects of Wearing a Powered Device: Powered Ankle-Foot Prosthesis on Amputee ankle-foot prosthesis Walking Efficacy study NCT00869947 Pain Relief After Forefoot Surgery Device: Catheter RCT, safety/efficacy study NCT01019005 Causes and treatments in mechanically induced foot pain RCT ISRCTN77862746 Motorized Continuous Cold Therapy Versus Standard Post-op Icing Protocol for Two Foot and Ankle Procedures Phase IV: RCT, efficacy study NCT00950183 Negative Pressure Wound Dressing Study RCT, efficacy study NCT01366105 A Double-blind RCT of a Single Dose of Hyaluronan in the Treatment of Osteoarthritis of the Ankle RCT, efficacy study NCT01243814 Plantar Fasciosis, Achilles Tendinosis Adult Acquired Flatfoot Surgical Wound Infection Device: hyaluronate Osteoarthritis intra-articular injection; Device: placebo injection 317 http://ClinicalTrials.gov/show/NCT00869947 http://ClinicalTrials.gov/show/NCT01019005 http://www.controlledtrials.com/ISRCTN77862746 Achilles Tendinosis Study; Comparison of Radiofrequency to Surgical MicroDebridement Phase IV: RCT, efficacy study NCT00534781 Stability and 3D Motion Study of an Experimental Prosthetic Foot Phase III: RCT NCT00968292 Assessment of the Ability of Ionic Foot Bath (IonCleanse®) to Remove Heavy Metals Through the Feet and Its Potential Impact on Body Burden of Heavy Metals Single group assignment, efficacy study NCT01125592 Clinical Trial of Tensegrity Prosthetics K3 Promoter Foot Prosthesis Phase II/III: RCT, efficacy study NCT00888199 Evaluation of the Efficiency of the Echelon Foot in Traumatic Trans Tibial Amputees Phase I/II: Single group assignment NCT01004926 GEM OS™1 Bone Graft Compared to Autologous Bone Graft in Foot and Ankle Fusions RCT, safety/efficacy study NCT00583375 Drugs including biologics Ketorolac Effects on Postoperative Pain and Bone Healing RCT, efficacy study NCT01133639 Device: plasma Achilles Pain; Wdrwn microdebrider; Achilles Tendinosis; Procedure: Heel Pain Mechanical Surgical Debridement Device: Experimental Amputation Not yet prosthetics foot (K3 Rec Promoter) 60 Adt Sep-07 Sep-10 ArthroCare Sen Corporation http://ClinicalTrials.gov/show/NCT00534781 50 Adt May-10 Aug-10 Tensegrity Sen Prosthetics http://ClinicalTrials.gov/show/NCT00968292 Device: IonCLeanse Healthy Footbath Comp 6 Child May-10 Jul-10 The Canadian Adt College of Sen Naturopathic Medicine http://ClinicalTrials.gov/show/NCT01125592 Device: Experimental Amputation prosthetic foot (K3 Promoter) Not yet Rec 80 http://ClinicalTrials.gov/show/NCT00888199 Device: Echelon foot Unilateral Trans Tibial Amputation Not yet Rec 10 Adt Jan-10 Jun-10 Tensegrity Sen Prosthetics; National Institutes of Health Adt Oct-09 Mar-10 Sheba Medical Sen Center Device: GEM OS1; Foot Fusion Procedure: Standard of Care Comp 396 Adt Apr-07 Feb-10 BioMimetic Sen Therapeutics http://ClinicalTrials.gov/show/NCT00583375 Rec 88 Adt May-10 May-13 Beth Israel http://ClinicalTrials.gov/show/NCT01133639 Deaconess Medical Center; American College of Foot and Ankle Surgeons Drug: Ketorolac; Drug: Placebo Bunion 318 http://ClinicalTrials.gov/show/NCT01004926 Regional Anesthesia for Major Drug: Nerve Block Surgery of the Foot. levobupivacaïne 0,5 Levobupivacaïne Ropivacaine %; Drug: ropivacaïne 0.5% Versus 0.5% in the Sciatic 0,5 % Block Through médiofémorale Phase IV: RCT, efficacy study NCT00956709 Side Effects of Autologous Biological: Osteoarthritis Mesenchymal Stem Cell mesenchymal stem Transplantation in Ankle Joint cell Osteoartritis Phase I: Single group assignment, safety study NCT01436058 Treatment of Plantar Fasciitis With Biological: platelet Plantar Fasciitis Platelet Rich Plasma rich plasma; Drug: RCT, efficacy study corticosteroid NCT01127672 injection TENDOSHOCK-2010 Combination Drug: Polidocanol; Tendinopathy; Therapy for Athletic Device: Focused Epicondylitis; Tendinopathies extracorporeal shock Achilles, Patella, Phase II: Single group wave therapy; Drug: Elbow assignment, safety/efficacy Topical NO; study Behavioral: Painful NCT01185951 eccentric training in Achilles tendinopathy; Behavioral: Painful eccentric training for patella tendinopathy on 25° decline board; Behavioral: Painful eccentric training for elbow tendinopathy using Thera-Band Flex-Bar A Study Comparing Etoricoxib and Drug: etoricoxib; Hallux Valgus; Diclofenac Sodium in Post Hallux Drug: Diclofenac Postoperative Pain Valgus Surgery Pain Phase IV: RCT, safety/efficacy study NCT01190722 Rec 42 Adt Dec-08 Oct-11 Nantes University Hospital http://ClinicalTrials.gov/show/NCT00956709 Comp 6 Adt Sep-10 Sep-11 Royan Institute http://ClinicalTrials.gov/show/NCT01436058 Not yet Rec 50 Adt May-10 May-11 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT01127672 Active, NR 114 Adt Jan-07 Dec-10 Hannover Sen Medical School http://ClinicalTrials.gov/show/NCT01185951 Adt Nov-10 Jul-10 Karolinska Institutet http://ClinicalTrials.gov/show/NCT01190722 Wdrwn 200 319 Procedure Treatment Outcomes for Ankle Arthritis Prospective, cohort study NCT00391365 Procedure: Gait analysis Osteoarthritis Ultrasound Guided Ankle Block Procedure: Pain Relief After Versus Medial Forefoot Block for Ultrasound guided Forefoot Surgery Forefoot Surgery ankle block; RCT, efficacy study Procedure: Medial NCT01386320 forefoot block A Randomized Trial to Evaluate Procedure: Flexor Achilles the Effectiveness of Transferring Hallucis Longus Tendinopathy the Flexor Hallucis Longus Tendon Tendon transfer; Phase IV: RCT, safety/efficacy Procedure: Transfer study of the Flexor Hallucis NCT01341509 Longus Tendon; Procedure: No transfer of Flexor Hallucis Longus tendon Placement of Perineural Catheters Procedure: Foot Surgery in the Popliteal Region Placement of Phase IV: RCT, safety/efficacy perineural catheters study with NCT01546077 Hydrolocalization technique using Rec 500 Rec 60 Rec 20 Adt Apr-11 Apr-14 OAD Sen Orthopaedics Rec 40 Adt Jan-12 Mar-13 Attikon Hospital http://ClinicalTrials.gov/show/NCT01546077 Sen 320 Adt Oct-06 Sep-15 Department of http://ClinicalTrials.gov/show/NCT00391365 Sen Veterans Affairs; Orthopaedic Associates of Michigan, PC; Orthopedic & Fracture Clinic; Minnesota Orthopedic Sports Medicine Institute Twin Cities Orthopedics Adt Feb-11 Oct-14 Hull and East http://ClinicalTrials.gov/show/NCT01386320 Sen Yorkshire Hospitals NHS Trust http://ClinicalTrials.gov/show/NCT01341509 Continuous Popliteal Nerve Blocks: Effect of Perineural Catheter Tip Location Relative to the Sciatic Nerve Bifurcation on Postoperative Analgesia Phase IV: RCT, safety/efficacy study NCT01229696 Ankle Block Versus Popliteal Fossa Block as Primary Anesthesia for Forefoot Surgical Procedures Phase IV: RCT, efficacy study NCT01376960 Prevention of Phantom Limb and Stump Pain Using Ambulatory Continuous Peripheral Nerve Blocks Phase IV: RCT, safety/efficacy study NCT00771862 Popliteal Sciatic Nerve Block Catheter Placement for Foot Surgery RCT NCT01049906 Ultrasound-Guided Continuous Sciatic Nerve Blocks: Popliteal Versus Subgluteal Catheters Phase IV: RCT, pharmacodynamics study NCT01325012 Saphenous Nerve Block: Single Shot Versus Continuous Infusion to Supplement a Continuous Sciatic Nerve Block After Major Ankle Surgery RCT, efficacy study NCT01445210 Procedure: Catheter Placed At Bifurcation; Procedure: Catheter Placed 5cm Above Bifurcation Popliteal Nerve Block; Foot Surgery; Ankle Surgery; Popliteal Bifurcation Rec 150 Adt Oct-10 Dec-12 University of Sen California, San Diego Procedure: elective forefoot surgery Anesthesia; Forefoot Surgery Rec 101 Child Jun-11 Dec-12 OrthoCarolina Adt Research Sen Institute, Inc. http://ClinicalTrials.gov/show/NCT01229696 http://ClinicalTrials.gov/show/NCT01376960 Procedure: Amputation; Active, perineural ropivicaine Phantom Limb Pain; NR Stump Pain 18 Procedure: Foot Surgery; Ankle Placement of nerve Surgery block catheter; Procedure: Placement of nerve block catheter Procedure: Foot Surgery Subgluteal Sciatic Nerve Block; Procedure: Popliteal Sciatic Nerve Block Active, NR 124 Rec 40 Adt Mar-11 Dec-12 University of Sen California, San Diego Rec 50 Adt Sep-11 Jul-12 University of http://ClinicalTrials.gov/show/NCT01445210 Sen Aarhus; Aarhus University Hospital Procedure: Continuous saphenous nerve block; Procedure: Placebo Major Ankle Surgery 321 Adt Oct-08 Dec-12 University of http://ClinicalTrials.gov/show/NCT00771862 Sen California, San Diego; National Institute of General Medical Sciences (NIGMS) Adt Oct-09 Dec-12 Mayo Clinic http://ClinicalTrials.gov/show/NCT01049906 Sen http://ClinicalTrials.gov/show/NCT01325012 Chronic Insertional Achilles Procedure: Achilles Tendonitis Treated With or Without decompression & Flexor Hallucis Longus Tendon debridement; Transfer Procedure: Achilles Phase IV: RCT, efficacy study decompression and NCT00950053 debridement with FHL transfer Ambulatory Continuous Peripheral Procedure: Nerve Blocks for Treatment of perineural Post-Amputation Phantom Limb ropivacaine and Stump Pain RCT, efficacy study NCT00667264 Effectiveness of extracorporeal shock wave therapy in patients with proximal plantar fasciitis RCT ISRCTN49594569 Eccentric Exercise for Chronic Mid-portion Achilles Tendinopathy RCT, efficacy study NCT01225497 Chronic Insertional Achilles Tendonitis Active, NR 52 Adt Dec-08 Jun-12 OrthoCarolina Sen Research Institute, Inc. Amputation; Phantom Limb; Stump Pain Comp 7 Radial extracorporeal Chronic plantar shock wave therapy; fasciitis No active treatment Comp 68 Adt Oct-08 Dec-11 University of http://ClinicalTrials.gov/show/NCT00667264 Sen California, San Diego; Summit Medical; National Institute of General Medical Sciences Adt Sep-09 Sep-11 The Hong Kong http://www.controlledPolytechnic trials.com/ISRCTN49594569 University (China) Achilles Tendon; Tendinopathy Not yet Rec 52 Adt Nov-10 Feb-11 Queen Margaret http://ClinicalTrials.gov/show/NCT01225497 Sen University Sciatic Nerve Blockade for Foot/Ankle Surgery Comp 64 Adt May-09 Dec-10 University Health http://ClinicalTrials.gov/show/NCT00802581 Sen Network, Toronto Hallux Valgus Invite 40 Adt Sep-08 Dec-10 Frederiksberg Sen University Hospital Procedure: Standard eccentric exercise; Procedure: Eccentric exerciseExperimental group Circumferential Spread of Procedure: Anesthetic and Success in Sciatic Circumferential Nerve Blockade spread of local RCT, efficacy study anesthetic; NCT00802581 Procedure: Noncircumferential spread of local anesthetic Home Infusors for Analgesia After Procedure: Foot Surgery elastomeric pump Phase IV: RCT, efficacy study with reservoir of 500 NCT00600899 ml, infusion rate of 8 ml/h; Procedure: elastomeric pump with reservoir of 275 ml, infusion rate of 5 ml/h 322 http://ClinicalTrials.gov/show/NCT00950053 http://ClinicalTrials.gov/show/NCT00600899 The CARROT trial: CAllus Reduction Reinforcing Orthotic Therapy RCT, efficacy study ISRCTN05190231 Effectiveness of radial shock wave treatment or tissue-specific plantar fascia-stretching in patients with chronic plantar heel pain RCT ISRCTN11644582 Other DeNovo NT Ankle LDC Study Cohort study NCT01347892 Prospective Randomized Evaluation of a Two and Three Piece Total Ankle Replacement Phase IV: RCT NCT01504438 Study of the Effect of Weight Bearing Status on Patient Outcomes After Surgery for Osteochondral Defects of the Ankle RCT NCT01405664 Sensory-Targeted Ankle Rehabilitation Strategies (STARS) Phase II: RCT, efficacy study NCT01541657 Callus debridement + Rheumatoid arthritis usual longterm therapies; usual longterm therapies only Plantar fasciaPlantar fasciopathy specific stretching (PFSS); Radial shock wave therapy (RSWT); PFSS + RSWT Comp 64 Child Oct-07 Oct-10 Leeds Teaching http://www.controlledAdt Hospital NHS trials.com/ISRCTN05190231 Sen Trust (UK) Comp 250 Adt Sen Other: DeNovo NT Articular Cartilage Natural Tissue Graft Lesions or Defects; Osteochondral Lesions; Osteochondritis Dissicans Other: Total Ankle Ankle Osteoarthritis Replacement Surgery Rec 250 Adt Mar-11 Sep-18 Zimmer Sen Orthobiologics, Inc. Rec 50 Adt Oct-11 Feb-16 Duke University http://ClinicalTrials.gov/show/NCT01504438 Sen Other: WeightOsteochondritis Bearing as Tolerated Dissecans of Ankle and Joints of Foot Not yet Rec 68 Child Sep-11 Sep-13 Capital District http://ClinicalTrials.gov/show/NCT01405664 Adt Health Authority, Canada Rec 80 Adt Dec-11 Apr-13 University of http://ClinicalTrials.gov/show/NCT01541657 Kentucky; University of North Carolina, Charlotte; National Institute of Arthritis and Musculoskeletal and Skin Diseases Other: Ankle Joint Mobilization; Other: Foot Massage; Other: Calf Stretching Chronic Ankle Instability 323 Jul-07 Jan-10 OrthoTrauma Evaluation Center (Germany) http://www.controlledtrials.com/ISRCTN11644582 http://ClinicalTrials.gov/show/NCT01347892 Surgical Treatment for Hallux Rigidus Non-randomized, efficacy study NCT01048450 Radiation: Joint Resection- Keller Procedure; Procedure: Joint Fusion; Procedure: Hemi-metallic Joint Implant Miscellaneous observational studies Neuro-orthopaedic Surgery in the Treatment of the Spastic Equinovarus Foot Prospective, case-only study NCT01265238 Short Term Follow-up of Patent Implanted With the B-BOP Lock Plate Prospective, cohort study NCT01284998 Microcirculatory Mapping of the Aging Hand and Foot Prospective, cohort study NCT01235312 Hallux Limitus; Hallux Rigidus Comp 158 Adt Sen Rec 50 Adt Dec-09 Dec-12 University http://ClinicalTrials.gov/show/NCT01265238 Sen Hospital of MontGodinne Hallux Valgus; Active, Hallux Varus; NR Vicious Callus on M1 80 Adt Jun-09 Jul-12 Integra Sen LifeSciences Services http://ClinicalTrials.gov/show/NCT01284998 Cutaneous Microcirculation in Vascular Diseases Comp 120 Adt Sep-10 May-11 Hannover Sen Medical School http://ClinicalTrials.gov/show/NCT01235312 Conditions Recruit n Age Start (Grp) Date Femur Fracture Active, NR 33 Child Nov-07 Dec-13 Biomet, Inc. Muscle Spasticity; Spastic Foot (Finding); Stroke Jul-09 Jun-11 American College of Foot and Ankle Surgeons http://ClinicalTrials.gov/show/NCT01048450 A11. LOWER LIMB A11A: PAEDIATRICS Title Interventions Phases: trial design (control) CT ID Device Pediatric Locking Nail for the Device: Pediatric Treatment of Femoral Fractures in Locking Nail Children Prospective, cohort study NCT00725894 324 End Sponsors Date URL http://ClinicalTrials.gov/show/NCT00725894 Drugs including biologics Efficacy Study of Femoral Nerve Block in Children With a Femur Fracture RCT NCT01294098 Spinal anaesthesia in adolescent population with 2-chloroprocaine 1% for lower limb procedures of short duration: a prospective, randomised, blind-observer, dosefinding study RCT, safety/efficacy study ISRCTN57987506 Botulinum toxin: an adjunct in limb reconstruction - Can it reduce pain and joint complications in the lengthening phase? RCT ISRCTN35609758 Drug: Marcaine Femoral Fractures; Pain, Postoperative Invite 180 Child Feb-11 Feb-13 Washington University School of Medicine http://ClinicalTrials.gov/show/NCT01294098 2-chloroprocaine Short duration (less hydrochloride at 1% than 40 minutes) concentration: 0.206 lower limb surgery mg/cm; 0.235 mg/cm; 0.265 mg/cm. Active 96 Child Mar-11 Oct-12 Sintetica S.A. (Switzerland) http://www.controlledtrials.com/ISRCTN57987506 Botulinum toxin intramuscular injections; Saline injections Limb reconstruction surgery; femoral or tibial deformity; congenital talipes equinovarus Comp 36 Child Apr-08 Apr-10 Sheffield http://www.controlledChildren's NHS trials.com/ISRCTN35609758 Foundation Trust (UK) Femoral Fractures Invite 145 Child Jun-09 Jun-13 Washington http://ClinicalTrials.gov/show/NCT00943332 University School of Medicine; University of MissouriColumbia; Children's Mercy Hospital-Kansas City, MO 25 Child Aug-07 Jun-11 University of http://ClinicalTrials.gov/show/NCT00175591 British Columbia Procedure Pediatric Femur Research Project Procedure: femur Prospective, cohort study fracture repair NCT00943332 The Effect of Femoral Nerve Block on Opioid Requirements After Surgery for a Femur Fracture in Children Phase I: RCT, safety/efficacy study NCT00175591 Procedure: Pain, Postoperative Administration of a femoral nerve block (bupivacaine HCL) Term 325 Distal Rectus Femoris Transfer as a Part of Multilevel Surgery in Children With Spastic Diplegia RCT NCT01381198 Simultaneous Lengthening of Bilateral Femora and Tibiae in Achondroplastic Patients Single group assignment, efficacy study NCT01328418 Study of Tibial Shaft Fractures in Children RCT NCT01238523 Procedure: Distal rectus femoris transfer Cerebral Palsy Comp 36 Child Jun-07 May-11 University of Heidelberg Procedure: Lengthening over nail SHOX Gene With Short Stature Comp 22 Child Apr-02 Mar-11 Bilen, Fikri Erkal, http://ClinicalTrials.gov/show/NCT01328418 M.D. Procedure: Long leg Tibial Shaft Comp cast in full extension; Fractures in Children Procedure: Long leg cast with 45 degrees of flexion 81 Child May-07 May-10 University of http://ClinicalTrials.gov/show/NCT01238523 California, Los Angeles; Los Angeles Orthopaedic Hospital Child Apr-08 Apr-10 Sheffield http://www.controlledChildren's NHS trials.com/ISRCTN35609758 Foundation Trust (UK) Botulinum toxin: an adjunct in limb Botulinum toxin reconstruction - Can it reduce pain intramuscular and joint complications in the injections; Placebo lengthening phase? RCT ISRCTN35609758 Titanium Elastic Nailing Versus Hip Procedure: titanium Spica Cast in Treatment of elastic nailing; Femoral Fractures in Children Device: Hip spica Phase II: Non-randomized, casting efficacy study NCT01190696 Miscellaneous observational studies Evaluation of the Change in Length of the Leg in Children After Treatment of Femur Fractures. Phase II: Prospective, cohort study NCT00355420 Femoral or tibial deformity; Congenital talipes equinovarus. Comp 36 Femoral Shaft Fracture Comp 46 Fractures Active, NR http://ClinicalTrials.gov/show/NCT01381198 Child Feb-09 Jan-10 Isfahan University of Medical Sciences http://ClinicalTrials.gov/show/NCT01190696 N/K Child Oct-06 Sep-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00355420 326 A11B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Device A Multicenter Randomized Trial Comparing IM Nails and Plate Fixation in Proximal Tibial Fractures RCT, efficacy study NCT00429585 A Multicenter Randomized Trial Comparing IM Nails and Plate Fixation in Distal Femur Fractures RCT, efficacy study NCT00429663 rhBMP-2 Versus Autograft in Critical Size Tibial Defects Phase IV: RCT, safety/efficacy study NCT00853489 Interventions Conditions Device: reamed, interlocking intramedullary nail; Device: locking periarticular plate Tibial Fractures TRial to Evaluate UltraSound in the Treatment of Tibial Fractures RCT, efficacy study NCT00667849 Device: Exogen Bone Healing System Device: reamed, Femoral Fractures interlocking intramedullary nail; Device: locking periarticular plate Device: recombinant Tibial Fractures human bone morphogenetic protein 2 (rhBMP-2) (INFUSE); Procedure: Autogenous iliac crest bone graft Tibial Fractures Recruit n Rec 160 Rec 160 Child Feb-07 Dec-14 Boston Medical http://ClinicalTrials.gov/show/NCT00429663 Adt Center Sen Not yet Rec 50 Rec 500 327 Age Start (Grp) Date End Sponsors Date URL Adt Feb-07 Dec-14 Boston Medical http://ClinicalTrials.gov/show/NCT00429585 Sen Center Adt Aug-11 Aug-14 St. Louis http://ClinicalTrials.gov/show/NCT00853489 University; Department of Defense, Orthopaedic Extremity Trauma Research Program (OETRP); Major Extremity Trauma Research Consortium Adt Sep-08 Dec-12 Smith & http://ClinicalTrials.gov/show/NCT00667849 Sen Nephew, Inc.; Canadian Institutes of Health Research The Efficacy and Cost Device: Cryotherapy; Proximal Tibia Effectiveness of Preoperative and Device: Room Fracture Postoperative Cryotherapy in temperature cuff Proximal Tibia Fractures Phase III: RCT, efficacy study NCT01104831 Trial to Evaluate the Effectiveness of Angular Stable Locking System (ASLS) in Patients With Distal Tibial Fractures RCT, efficacy study NCT00875992 TRIGEN SURESHOT™ Distal Targeting System Study Phase III: RCT, safety/efficacy study NCT01327508 Device: ETN with Tibial Fractures ASLS; Device: ETN locked with conventional locking bolts Device: TRIGEN Femoral Shaft SURESHOT Distal Fracture Targeting Instrumentation.; Other: Free hand Technique Lateral Versus Anterior Spanning Device: Anterior pin Fractures, Closed External Fixator for Tibial Plateau placement; Device: Fractures Lateral pin RCT, efficacy study placement NCT00610701 Use of a Reinforced Injectable Device: Norian Tibial Fractures Calcium Phosphate Bone Cement Drillable Bone Void in the Treatment of Tibial Plateau Filler Fractures Prospective, case-only study NCT01132508 The Development of a Surgical Device: Target Tape Femoral Fracture; Localizing Aid Medical Device Tibial Fracture RCT, safety/efficacy study NCT01300520 New Method for Distal Interlocking Device: The Guiding Fracture; tibia of Cannulated Intramedullary Nails Star; Device: Phase I/II: RCT, safety/efficacy fluoroscopy (OEC study 9800 - General NCT00648479 Electric) Rec Active, NR 110 Child Apr-10 Nov-12 University of http://ClinicalTrials.gov/show/NCT01104831 Adt Manitoba; Sen Orthopedic Research and Education Foundation; Orthopedic Trauma Association 140 Adt Jun-09 Nov-12 AO Clinical http://ClinicalTrials.gov/show/NCT00875992 Sen Investigation and Documentation; Synthes Inc. Rec 140 Adt Apr-11 Apr-12 Smith & Sen Nephew, Inc. http://ClinicalTrials.gov/show/NCT01327508 Rec 100 Adt Mar-06 Mar-12 University of Sen MissouriColumbia http://ClinicalTrials.gov/show/NCT00610701 Rec 30 Adt Sep-08 Mar-12 Synthes GmbH; http://ClinicalTrials.gov/show/NCT01132508 Sen Synthes Asia Pacific Not yet 250 Child Mar-11 Dec-11 Aeos Biomedical http://ClinicalTrials.gov/show/NCT01300520 Rec Adt Inc. Sen Term 10 328 Adt N/K Dec-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT00648479 Plate Fixation of Distal Femur Device: 95-degree Femoral Fractures Fractures: A Protocol for a Study Angled Blade Plate; of Two Plate Options Device: 4.5mm Prospective, case-only study Condylar Locking NCT00644397 Plate Functional Outcome and MRI of Device: Femoral Femoral Shaft Muscle Damage Following Nailing Nailing with Different Fracture Procedure in Femur (Thigh) Entry Points Fractures Using Different Entry Points Single group assignment, efficacy study NCT00471913 Intramedullary Nailing of the Device: Antegrade Femur Fracture Femur:Trochanteric vs Piriformis Intramedullary Nail; Starting Portals Device: Trigen RCT, efficacy study Trochanteric Femoral NCT00593333 Nail Randomized, Prospective Device: Synthes Femur Fracture Comparison of Two Femoral Reamer-IrrigatorReaming Systems Aspirator (RIA); RCT, efficacy study Device: Zimmer NCT00594438 Sentinel Reamer Pulsed Ultrasound to Speed-up Pulsed, lowClosed or I° open Healing after Intramedullary nailing energetic ultrasound fractures of the tibia of Tibia fractures (Exogen, Smith & RCT, efficacy study Nephew); usual care ISRCTN90844675 Continuous Pressure Monitoring In Lower Leg Fractures RCT, efficacy study NCT00358514 Natural History of Anterior Compartment Pressures of the Thigh Following Femur Fracture Single group assignment NCT00919464 Rec Comp 60 Adt Active, NR 116 Active, NR 20 Adt Jun-03 Dec-10 University of Sen Alabama at Birmingham; Smith & Nephew, Inc. Adt Jan-07 Dec-10 University of Alabama at Birmingham; Synthes Inc. Comp 250 Device: Continuous Compartment Compartment Syndrome Pressure Monitoring Term Device: Pressure monitoring device Term Femur Fracture 100 Child May-06 Jul-11 MetroHealth Adt Medical Center Sen http://ClinicalTrials.gov/show/NCT00644397 Apr-07 Apr-11 University of http://ClinicalTrials.gov/show/NCT00471913 British Columbia http://ClinicalTrials.gov/show/NCT00593333 http://ClinicalTrials.gov/show/NCT00594438 Adt Oct-08 Oct-10 German http://www.controlledSen Employer's trials.com/ISRCTN90844675 Liability Insurance for the Administrative Professions (Germany) 250 Child Sep-08 Mar-10 University of http://ClinicalTrials.gov/show/NCT00358514 Adt British Columbia Sen 7 329 Adt Apr-06 Jan-10 CAMC Health Sen System http://ClinicalTrials.gov/show/NCT00919464 Drugs including biologics Effect of C1-esterase Inhibitor on Drug: C1-esterase Trauma; Systemic Inflammation in Trauma inhibitor; Other: Inflammation; Patients With a Femur Fracture Saline 0.9% Sepsis; Multiple Phase III: RCT Organ Dysfunction NCT01275976 Syndrome Study of AMG 785 in Tibial Drug: AMG 785 Fracture Healing Diaphyseal Fractures Status Post 210mg; Drug: AMG Intramedullary Nailing 785 70mg; Drug: Phase II: RCT, safety/efficacy AMG 785 140 mg; study Drug: Placebo NCT00907296 Efficacy of strontium ranelate in Strontium ranelate Lower limb fracture, the management of limb fractures osteoporosis in osteoporotic patients Single group assignment, efficacy study ISRCTN60251236 Safety and Efficacy of I 0401 in the Drug: I-0401 (a new Tibia Plateau Treatment of Tibial Plateau bone graft substitute) Fractures Fractures Requiring Grafting Phase II: RCT, safety/efficacy study NCT00409799 Pain; Opiate; upper A Dosing and Efficacy Study of Drug: sufentanil or lower extremity Intra-nasal Sufentanil for Moderate fracture to Severe Pain Single group assignment, safety/efficacy study NCT01012999 Study Of Tranexamic Acid For The Drug: Tranexamic Femoral Fractures Reduction Of Blood Loss In Acid plus standard of Patients Undergoing Surgery For care; Procedure: Long Bone Fracture Standard of care Phase IV: RCT, efficacy study NCT00824564 Not yet Rec 70 Adt May-11 Oct-14 UMC Utrecht; Sen Sanquin http://ClinicalTrials.gov/show/NCT01275976 Rec 400 Adt Sep-09 Oct-13 Amgen Sen http://ClinicalTrials.gov/show/NCT00907296 Comp 40 Adt Jun-10 Dec-11 Institut de http://www.controlledSen Recherches trials.com/ISRCTN60251236 Internationales Servier (France) Active, NR 180 Adt Nov-06 Sep-11 Kuros Sen Biosurgery AG http://ClinicalTrials.gov/show/NCT00409799 Term 16 Adt Nov-09 Mar-11 University of Sen Utah http://ClinicalTrials.gov/show/NCT01012999 Comp 82 Adt http://ClinicalTrials.gov/show/NCT00824564 330 Apr-09 Jun-10 Pfizer ACTiF- Assessment of Closed Tibial Fractures Phase II: RCT, efficacy study NCT00533377 Drug: CP-533, 536; Tibial Fractures Drug: Placebo; Procedure: Standard of Care; Drug: CP533,536; Drug: CP533,536; Drug: CP533,536 A Phase 2/3 Multicenter, Drug: rhBMP-2/CPM; Fractures, Controlled Trial Of rhBMP-2/CPM Drug: rhBMP-2/CPM; diaphyseal tibial In Tibial Fractures Drug: rhBMP-2/CPM; fracture Phase II/III: RCT, safety study Drug: rhBMP-2/CPM NCT00387686 Procedure Wound management of Open Lower Limb Fractures (WOLLF) RCT ISRCTN33756652 Comparison of BioCart™II With Microfracture for Treatment of Cartilage Defects of the Femoral Condyle Phase II: RCT, safety/efficacy study NCT00729716 Femoral Bone Metastases Single group assignment NCT01428895 Comp 276 Child Jan-08 May-10 Pfizer Adt Sen http://ClinicalTrials.gov/show/NCT00533377 Term 367 http://ClinicalTrials.gov/show/NCT00387686 Active 460 Child Mar-12 Mar-17 University of Adt Warwick (UK) Sen Adt Nov-06 Mar-10 Wyeth is now a Sen wholly owned subsidiary of Pfizer Negative-pressure wound therapy; Standard dressing Open fractures of the lower limb Procedure: BioCart™II; Procedure: Microfracture Symptomatic Cartilage Defects of the Femoral Condyle Rec 40 Child May-08 May-15 ProChon Biotech http://ClinicalTrials.gov/show/NCT00729716 Adt Ltd Procedure: Surgery Cancer; Metastatic Alone; Other: Malignant Neoplasm Combined Surgery to Femur; Risk of and Radiation Fracture therapy M.I.P.O. vs Intramedullary Nailing Procedure: Minimally Tibia Fracture in Tibia Fractures Invasive Plate RCT Osteosynthesis; NCT01047826 Procedure: intramedullary tibial Nailing Standard Reaming Versus Procedure: Standard Femoral Fractures Reaming/Irrigating/Aspirating for Reaming; Procedure: Intramedullary Nailing of Femoral Reaming/Irrigating/A Shaft Fractures spirating RCT NCT00534326 Rec 180 Adt Mar-09 Mar-15 University Health http://ClinicalTrials.gov/show/NCT01428895 Sen Network, Toronto Rec 180 Adt Dec-10 Dec-14 King Abdullah http://ClinicalTrials.gov/show/NCT01047826 International Medical Research Center Invite 550 Adt Dec-06 Dec-14 Greenville http://ClinicalTrials.gov/show/NCT00534326 Sen Hospital System University Medical Center 331 http://www.controlledtrials.com/ISRCTN33756652 Assessment of Fixation Strategies for Severe Open Tibia Fractures Phase III: RCT NCT01494519 Nails Versus Plates for Femur Fractures in Dar es Salaam, Tanzania Prospective, cohort study NCT01548456 Procedure: Surgery with an external ring fixator; Procedure: Definitive fixation with a locked IM nail or plate Procedure: Intramedullary Nailing; Procedure: Open Reduction Internal Fixation Severe Open Fractures of the Tibia (Shin) Bone Femoral Fractures Rec 624 Not yet 333 Rec Types of Fixation of Vancouver B1 Periprosthetic Fractures RCT NCT01354535 Adt Jul-11 Oct-14 Major Extremity http://ClinicalTrials.gov/show/NCT01494519 Trauma Research Consortium; Department of Defense Adt Jul-12 Jul-14 University of http://ClinicalTrials.gov/show/NCT01548456 California, San Francisco; Orthopaedic Research Foundation; Orthopaedic Trauma Association; Muhimbili Orthopaedic Institute Adt Jun-12 Jun-14 St. Michael's http://ClinicalTrials.gov/show/NCT01354535 Sen Hospital, Toronto Procedure: Isolated Femur Fractures Not yet 89 Locked Compression Rec Plate; Procedure: Cable Plating and Strut Allograft with Cerclage Wiring Hyperbaric Oxygen in Lower Leg Procedure: Tibial Fracture; Soft Rec 120 Adt Feb-06 Dec-13 Bayside Health Trauma Hyperbaric Tissue Injury Sen Phase II/III: RCT, efficacy study Oxygenation NCT00264511 Using autologous mesenchymal mesenchymal stem Tibial Fracture, non- Active 60 Adt Jan-10 Dec-13 Joint UCLH and stem cells (MSC) to treat human cells; bone marrow union Sen UCL Biomedical fractures Research Unit RCT (UK) ISRCTN09755245 Percutaneous Autologous Bone- Procedure: Tibial Fractures; Rec 186 Child Sep-07 Sep-13 University marrow Grafting for Open Tibial Osteosynthesis Fractures, Open; Adt Hospital, Tours Shaft Fracture Bone Marrow Sen RCT, efficacy study Transplantation NCT00512434 332 http://ClinicalTrials.gov/show/NCT00264511 http://www.controlledtrials.com/ISRCTN09755245 http://ClinicalTrials.gov/show/NCT00512434 Efficacy Study of Surgical Technique in Intramedullary Tibia Nailing, Using Trigen META Tibia Nails Phase IV: RCT, safety/efficacy study NCT01358292 Anterolateral Versus Posterior Approach for Total Hip Arthroplasty After Displaced Femoral Neck Fracture RCT, efficacy study NCT01484405 Suprapatellar Versus Infrapatellar Nailing in Tibial Fractures: A Pilot Study RCT, efficacy study NCT01341418 Distal Locking Using an Electromagnetic Field Guided Computer Based Real Time System for Orthopaedic Trauma Patients RCT, efficacy study NCT01183078 Fluid Lavage of Open Wounds (FLOW) RCT ISRCTN33993149 Procedure: Semiextended Surgical Technique Tibial Fractures Rec 200 Adt Feb-11 Jul-13 Smith & Nephew http://ClinicalTrials.gov/show/NCT01358292 Sen Orthopaedics AG Procedure: posterior Femur Fracture approach; Procedure: anterolateral approach Rec 64 Procedure: Suprapatellar approach; Procedure: Infrapatellar approach Procedure: freehand; Procedure: Wand technique Rec 40 Active, NR 48 Adt Jun-10 Jun-13 Florida http://ClinicalTrials.gov/show/NCT01484405 Sen Orthopaedic Institute; Orthopaedic Trauma Association Adt Apr-11 Sep-12 Florida http://ClinicalTrials.gov/show/NCT01341418 Sen Orthopaedic Institute; Orthopaedic Trauma Association Adt Aug-10 Feb-12 Wake Forest http://ClinicalTrials.gov/show/NCT01183078 Sen University; Smith & Nephew, Inc. Tibial Fractures. Tibial Fractures; Femoral Fractures Saline solution at Open fractures, gravity pressure (1-2 upper or lower psi); Saline solution extremity at low pressure (5-10 psi); Saline solution at high pressure (>20 psi); Castile soap solution (80ml per 3 litres saline) at gravity pressure (1 2 psi); Castile soap solution at low pressure (5-10 psi); Castile soap solution at high pressure (>20 psi) Comp 2280 Adt Jun-09 Jan-12 McMaster Sen University (Canada) 333 http://www.controlledtrials.com/ISRCTN33993149 Comparing Surgical Techniques for CRIF of Pertrochanteric Fractures RCT, safety/efficacy study NCT00686023 Procedure: internal fixation (DHS richard nail); Procedure: internal fixation (inflatable PFN by DISCOTEC) A Prospective Randomized Procedure: BMP-7 in Controlled Trial on the Use of adjunct to fresh Bone Morphogenetic 7 (BMP-7) frozen allograft; (OP-1®) and Demineralized Bone Procedure: allograft Matrix in Tibial Non-union together with DBM Phase IV: RCT, efficacy study NCT00551941 Adjunctive Therapy to Treat Tibial Procedure: open Shaft Fractures fracture reduction Phase II: RCT, safety/efficacy study NCT00533793 Pre-drilling or Self Drilling External Procedure: Fixation Pins Placement of Single group assignment, external fixation pins efficacy study NCT01046747 Autologous Implantation of Procedure: Mesenchymal Stem Cells for the autologous Treatment of Distal Tibial mesenchymal stem Fractures cells implantation Phase I/II: RCT, safety/efficacy study NCT00250302 A Study of Immediate and Delayed Procedure: delayed Closure of Type II and IIIa Open closure; Procedure: Tibia Fractures immediate wound Parallel assignment, efficacy closure study NCT01315392 Femur Fracture Non-union Diaphysary Tibial Fractures Trauma Fracture; Dislocation Tibial Fracture Not yet 100 Rec Adt Jun-08 Jan-12 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT00686023 Rec 30 Adt Oct-07 Dec-11 University http://ClinicalTrials.gov/show/NCT00551941 Sen Hospital, Ghent Active, NR 200 Adt Apr-07 Sep-11 Kuros http://ClinicalTrials.gov/show/NCT00533793 Sen Biosurgery AG; Baxter BioScience Rec 100 Adt Sen Jul-09 Aug-11 Temple University Comp 24 Adt Apr-09 Apr-11 Hadassah http://ClinicalTrials.gov/show/NCT00250302 Medical Organization; Teva Pharmaceutical Industries Type II and IIa Open Comp Tibia Fractures http://ClinicalTrials.gov/show/NCT01046747 451 Child Jul-00 Mar-11 Carolinas http://ClinicalTrials.gov/show/NCT01315392 Adt Healthcare Sen System; Orthopaedic Trauma Association; Orthopaedic Research and Education Fund 334 A randomised clinical pilot trial comparing intramedullary nailing with plate and screw fixation in the treatment of patients with an acute fracture of the distal tibia RCT ISRCTN08249684 Comparison Between LISS Plating and Intramedullary (IM) Nailing for Supracondylar Femur Fractures RCT, efficacy study NCT00578019 Skeletal Versus Cutaneous Traction For Treatment of Femur Fractures RCT, efficacy study NCT00916136 Intramedullary nailing; Screw and plate fixation Distal tibia fractures Comp 24 N/K Mar-08 Sep-10 University of Warwick (UK) http://www.controlledtrials.com/ISRCTN08249684 Procedure: IM Nailing; Procedure: LISS Supracondylar Femur Fracture Active, NR 80 Adt Dec-99 Sep-10 University of Sen Alabama at Birmingham http://ClinicalTrials.gov/show/NCT00578019 Rec 150 Adt May-09 May-10 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT00916136 Rec 460 Sen Mar-10 Jun-15 Karolinska Institutet http://ClinicalTrials.gov/show/NCT01141894 Not yet Rec 32 Child Apr-08 Apr-11 Imperial College http://ClinicalTrials.gov/show/NCT00632034 Adt London Sen Rec 20 Adt Dec-08 Dec-10 University of Sen MissouriColumbia; Medtronic Procedure: Femoral Femur Fracture Traction Other Goal Directed Haemodynamic Other: fluid and Therapy for Patients With Proximal inotropic support Femoral Fracture RCT, efficacy study NCT01141894 Stem Cells and Tibial Fractures Other: CD34+ Phase I/II: RCT, safety/efficacy haemopoietic stem study cells NCT00632034 Incisional Vacuum Assisted Other: 75 mmHg Closure (IVAC) Device and Its suction; Other: 125 Effect on Implanted Bone mmHg Morphogenic Protein (BMP-2) RCT NCT00829621 Miscellaneous observational studies Pilon Fracture Reduction and Functional Outcome Prospective, case control study NCT01316289 Femoral Fracture Tibial Fractures Fractures, Closed; BMP-2; Incisional Vacuum Assisted Closure (IVAC); Tibial fracture Pilon Fracture of Tibia Not yet 109 Rec 335 http://ClinicalTrials.gov/show/NCT00829621 Adt Nov-11 Sep-18 AO Clinical http://ClinicalTrials.gov/show/NCT01316289 Sen Investigation and Documentation A Comparison of Two Injection Locations in Obese Patients Having Lower Leg/Foot Surgery Prospective, cohort study NCT01550094 Onset Time of Nerve Block: A Comparison of Two Injection Locations in Patients Having Lower Leg/ Foot Surgery Prospective, cohort study NCT01542840 Inflammatory Response Following Intraarticular Fracture Prospective, case control study NCT01514643 Assessment of Severe Extremity Wound Bioburden at the Time of Definitive Wound Closure or Coverage Prospective, cohort study NCT01496014 Strain of Muscle &/or Rec Tendon of Lower Leg; Fracture of Lower Leg; Crushing Injury of Lower Leg; Fracture Malunion (Ankle &/or Foot); Complete Tear, Ankle &/or Foot Ligament; Pathological Fracture (Ankle &/or Foot); Loose Body in Joint of Ankle &/or Foot Strain of Muscle Not yet and/or Tendon of Rec Lower Leg; Fracture of Lower Leg; Crushing Injury of Lower Leg; Fracture Malunion - Ankle and/or Foot; Disorder of Joint of Ankle and/or Foot; Complete Tear, Ankle and/or Foot Ligament; Pathological Fracture - Ankle and/or Foot; Loose Body in Joint of Ankle and/or Foot Tibial Plateau Active, Fracture NR 80 Adt Mar-12 Mar-14 Jose Soberon, Sen MD 76 Adt Mar-12 Mar-14 Ochsner Health http://ClinicalTrials.gov/show/NCT01542840 Sen System 60 Adt Dec-11 Dec-13 University of Utah Open Fracture; tibial fracture 600 Adt Sep-11 Dec-13 Major Extremity http://ClinicalTrials.gov/show/NCT01496014 Trauma Research Consortium; Department of Defense Rec 336 http://ClinicalTrials.gov/show/NCT01550094 http://ClinicalTrials.gov/show/NCT01514643 The Role of Patient Expectations in Traumatic Orthopedic Outcomes-TEFTOM EURASIA Prospective study NCT01134354 Early Standardized Weight Bearing Utilizing Immersion Therapy Following Periarticular Lower Extremity Fractures Prospective, case control study NCT01457326 Pilon Fracture Reduction and Functional Outcome Prospective, case control study NCT01316289 Tibia Fracture (Isolated); Ankle Fracture (Isolated) Lower Extremity Periarticular Fractures Rec 200 Adt Jun-10 Oct-13 AO Clinical http://ClinicalTrials.gov/show/NCT01134354 Sen Investigation and Documentation Invite 130 Adt Jun-09 May-13 University of Sen Utah http://ClinicalTrials.gov/show/NCT01457326 Pilon Fracture of Tibia Not yet 109 Rec Adt Nov-11 Sep-18 AO Clinical http://ClinicalTrials.gov/show/NCT01316289 Sen Investigation and Documentation Interventions Conditions Recruit n Device: Open implantation of INFUSE Bone Graft (rh BMP-2); Procedure: Open implantation of ICBG Device: C leg compared to subject's mechanical leg (Otto Bock); Device: C leg compared to subject's mechanical leg (Otto Bock) Tibial Delayed Healing Rec 360 Adt Nov-10 Nov-15 Medtronic Spinal http://ClinicalTrials.gov/show/NCT01016067 Sen and Biologics Transfemoral Amputation; Unilateral Traumatic Amputation of Leg at or Above Knee Rec 40 Adt Aug-11 Dec-13 Rehabilitation http://ClinicalTrials.gov/show/NCT01537211 Sen Institute of Chicago; Otto Bock Healthcare A11C: OTHER Title Phases: trial design (control) CT ID Device Tibial Delayed Healing Pivotal Clinical Trial Phase III: RCT, safety/efficacy study NCT01016067 Functional Outcomes in Dysvascular Transfemoral Amputees RCT NCT01537211 337 Age Start (Grp) Date End Sponsors Date URL Effects of Shrinker Use on Healing Device: compression and Volume shrinker RCT, efficacy study NCT00693628 Senza™ spinal cord stimulation Senza™ spinal cord system for the treatment of chronic stimulation system back and leg pain in failed back surgery syndrome (FBSS) patients RCT ISRCTN33292457 SS) patients Study to Evaluate the Safety and Device: GelrinC Performance of Treatment of Articular Cartilage Lesions Located on the Femoral Condyle With gelrinC Phase I/II: Single group assignment, safety study NCT00989794 Strength, Pain and Function in Device: NMES Operation Iraqi Freedom/Operation (EMPI 300PV Enduring Freedom Amputees: A stimulator) plus Nurse-Managed Program standard of care RCT NCT00942890 Transtibial Amputation Rec 100 Adt Mar-07 Jan-13 University of Sen Oklahoma http://ClinicalTrials.gov/show/NCT00693628 Chronic back and leg pain in failed back surgery syndrome (FBSS) patients Active 20 Adt Apr-11 Dec-12 Nevro Sen Corporation (USA) http://www.controlledtrials.com/ISRCTN33292457 Femoral Condyle Lesion Rec 25 Adt Sep-09 Dec-12 Regentis Biomaterials http://ClinicalTrials.gov/show/NCT00989794 Transtibial Amputation Rec 60 Adt Evaluation of a Pro-Active Dynamic Accommodating Socket Cross-sectional, case-only study NCT01546311 Amputation Rec 5 Adt Sen Use of an Interactive Video Game Device: Nintendo Wii Below Knee as Part of a New Amputee fit ™ balance board Amputation Rehabilitation Program Single group assignment NCT01131819 Rec 10 Adt Sen Device: Pro Active Dynamic Accommodating Socket 338 Apr-09 Dec-12 University of http://ClinicalTrials.gov/show/NCT00942890 North Carolina, Charlotte; Walter Reed National Military Medical Center; United States Naval Medical Center, San Diego Jan-12 Dec-12 Infoscitex http://ClinicalTrials.gov/show/NCT01546311 Corporation; Liberating Technologies, Inc; Telemedicine and Advanced Technology Research Center (TATRC) May-10 Sep-12 University of http://ClinicalTrials.gov/show/NCT01131819 British Columbia Comparison of Two Under Knee Device: Lower Limb Bypass endothelialised Types:Endothelialised Prosthesis prosthesis Versus Autologous Vein Graft Phase II: RCT NCT00221806 Arteritis Evaluation of the Development of Device: Novel Evaluation of a New an Advanced, Conformable conformable woven Prosthetic Socket Prosthetic Socket, Study II inner socket Liner Material Cross-sectional, case-only study NCT01455324 Temporary Prosthesis in Traumatic Device: Temporary Below-knee Amputation tuber-ischii bearing Phase II: RCT, efficacy study; prosthesis NCT00263497 Clinical Evaluation of Direct Manufactured Prosthetic Sockets Phase II: RCT, efficacy study NCT01155024 Transtibial Amputation Device: Traditional Amputation fabricated prosthetic socket; Device: Direct manufactured (DM) prosthetic socket Rec 40 Comp 1 Rec 20 Comp 10 339 Adt Jun-04 Jun-12 University Sen Hospital, Bordeaux; Ministry of Health, France; W.L.Gore & Associates Adt Sep-11 Dec-11 Infoscitex Sen Corporation; U.S. Army Medical Research and Materiel Command; Mayo Clinic Child Mar-06 Dec-11 University Adt Hospital of North Norway; Medical University of Joenkoeping, Sweden; NCHADS Ministry of Health of Cambodia Adt Sep-10 Sep-11 Ohio Willow Sen Wood; Department of Defense http://ClinicalTrials.gov/show/NCT00221806 http://ClinicalTrials.gov/show/NCT01455324 http://ClinicalTrials.gov/show/NCT00263497 http://ClinicalTrials.gov/show/NCT01155024 The Effect of Reducing Soreness in Marathon Runners RCT, efficacy study NCT01512082 Device: Pulsed Soreness in Muscles Comp electromagnetic field devices; Device: Pulsed electromagnetic field devices 133 Comparison of Two Lower Limb Bypass Types : Prosthesis Versus Autologous Vein RCT, safety/efficacy study NCT00221715 Device: Arteritis; Diabetes femoropopliteal artery bypass; Device: femoropopliteal artery bypass Device: Monitoring of Compartment StO2 Syndrome Comp 100 Comp 120 Child Sep-09 Apr-11 University http://ClinicalTrials.gov/show/NCT00921271 Adt Hospital Sen Birmingham NHS Foundation Trust Device: adaptive prosthetic socket Active, NR 60 Adt Jan-09 Dec-10 University of Sen Wisconsin, Milwaukee http://ClinicalTrials.gov/show/NCT01108536 Rec 90 Adt http://ClinicalTrials.gov/show/NCT00681616 The Application of Near Infrared Spectroscopy (NIRS) in the Detection of Lower Limb Compartment Syndrome Prospective, cohort study NCT00921271 Dynamic Management of Excess Residual Limb Pressure With New Smart Socket Technology Single group assignment NCT01108536 Study of New Catheter & Pressure Monitor System to Help Prevent Compartment Syndrome From Developing in the Injured Leg RCT, safety/efficacy study NCT00681616 Amputation Device: Compartment Compartment Syndrome Monitoring System (CMS); Device: Compartment Monitoring System with Active Fluid Removal; Device: Compartment Monitoring System without fluid removal 340 Adt Aug-11 Aug-11 Northern http://ClinicalTrials.gov/show/NCT01512082 Sen Orthopaedic Division, Denmark; Department of Geriatrics, Aalborg Hospital, Aarhus University, Denmark; Department of Rheumatology, Aalborg Hospital, Aarhus University, Denmark Adt Jul-02 May-11 University http://ClinicalTrials.gov/show/NCT00221715 Sen Hospital, Bordeaux; Ministry of Health, France Jan-09 Dec-10 Twin Star Medical, Inc.; Department of Defense Medico Economic Evaluation of Dermal Substitute Integra® for Coverage of Inferior Limb Traumatic Skin Loss Phase III: RCT, safety/efficacy study NCT00906672 Negative Pressure Wound Dressing Study RCT, efficacy study NCT01366105 Metabolic Cost Savings for Transtibial Amputees Wearing the CESR Foot Phase III: RCT, efficacy study; NCT00494143 Drugs including biologics Local Infiltration Versus Block Against Pains After High Tibial Osteotomy Phase IV: RCT, safety/efficacy study NCT01537146 Evaluation of Continuous Saphenous Nerve Block to Supplement a Continuous Sciatic Nerve Block After Ankle Surgery RCT, efficacy study NCT01167907 Intraoperative Methadone vs Morphine for Postoperative Pain Control in Patients Undergoing Surgery of the Tibia RCT, efficacy study NCT01430182 Prophylactic Phenylephrine Infusion for Preventing Hypotension During Spinal Anesthesia Phase II: RCT, safety/efficacy study NCT01533662 Device: INTEGRA®; Leg Injuries; Ankle Procedure: Flap Injuries; Foot Injuries technique Rec 120 Adt Jun-09 Nov-10 University Sen Hospital, Bordeaux http://ClinicalTrials.gov/show/NCT00906672 Comp 106 Adt Aug-08 Oct-10 Georgetown Sen University http://ClinicalTrials.gov/show/NCT01366105 Device: CESR Transtibial Prosthetic Foot; Amputation Device: typical prosthetic foot; Device: standardized prosthetic foot Active, NR 20 Adt Sen Drug: Ropivacaine; Drug: Ropivacaine Osteoarthritis; Malalignment Active, NR 60 Adt Feb-12 Jun-14 Northern Sen Orthopaedic Division, Denmark http://ClinicalTrials.gov/show/NCT01537146 Drug: 0.2% ropivacaine; Drug: saline Orthopedic Surgery of Lower Extremity Rec 74 Adt Sen Jul-12 Wake Forest University; IFlow http://ClinicalTrials.gov/show/NCT01167907 Drug: Methadone; Drug: Morphine Pain, Postoperative Active, NR 60 Adt Sep-11 Mar-12 Baylor College of Medicine http://ClinicalTrials.gov/show/NCT01430182 Rec 64 Adt Mar-11 Mar-12 University Sen Hospital, Toulouse http://ClinicalTrials.gov/show/NCT01533662 Device: V.A.C. by K.C.I. Surgical Wound Infection Drug: phenylephrine Orthopedic Surgery infusion; Drug: of Lower Limb patients receiving saline infusion 341 Jul-07 Jun-10 Department of http://ClinicalTrials.gov/show/NCT00494143 Veterans Affairs; University of Michigan Jul-10 Study of Platelet-rich Plasma in Biological: platelet Cartilage Comp 50 Treating Patients With rich plasma injection Degeneration Tibiofemoral Cartilage Degeneration Single group assignment NCT01418755 Effects of Dexmedetomidine on Drug: Orthopedic/Podiatry Wdrwn 80 Tourniquet Pain Associated With Dexmedetomidine Procedures Lower Extremity Surgeries Under Hcl infusion; Drug: General Anesthesia normal saline Phase IV: RCT, efficacy study NCT00932386 A randomised, placebo controlled Perineural saline; Elective lower limb Comp 180 trial of levobupivacaine or the Perineural amputation combination of levobupivacaine levobupivacaine 1.25 and clonidine when administered mg/ml; Perineural as a sciatic perineural infusion for levobupivacaine 1.25 the prevention of phantom limb mg/ml and clonidine pain after lower limb amputation 1 mg/ml RCT, efficacy study ISRCTN31319378 Comparison of Postoperative Drug: Fentanyl; Post Operative Pain Comp 90 Analgesic Effect of Intrathecal Drug: Magnesium and Fentanyl Added to placebo(distilled Bupivacaine in Patients water); Drug: Undergoing Lower Limb magnesium sulphate Orthopedic Surgery Phase I/II: RCT, safety/efficacy study NCT01205997 Prospective, double-blind, Perineural infusion of Lower limb Comp 62 randomised trial to assess the levobupivacaine 1.25 amputation efficacy of continuous mg/ml; placebo sciatic/posterior tibial nerve blockade via a neural sheath catheter in lower limb amputees RCT (placebo), efficacy study ISRCTN68691928 342 Adt Jan-09 Jul-11 Komzak Martin, http://ClinicalTrials.gov/show/NCT01418755 Sen M.D. Adt Sen Jul-09 Jul-11 University of Medicine and Dentistry New Jersey http://ClinicalTrials.gov/show/NCT00932386 Adt Mar-07 Mar-11 NHS Tayside Sen (UK) http://www.controlledtrials.com/ISRCTN31319378 Adt Aug-10 Jan-11 Qazvin University Of Medical Sciences http://ClinicalTrials.gov/show/NCT01205997 Adt Sen http://www.controlledtrials.com/ISRCTN68691928 Jul-07 Jan-10 University Hospitals of Leicester NHS Trust (UK) Procedure Prevention of Phantom Limb and Stump Pain Using Ambulatory Continuous Peripheral Nerve Blocks Phase IV: RCT, safety/efficacy study NCT00771862 Intramedullary Femoral Reaming, Human Study RCT, efficacy study NCT01042132 Procedure: Amputation; Active, perineural ropivicaine Phantom Limb Pain; NR Stump Pain 18 Procedure: the effect of delayed intramedullary reaming; Procedure: the reaming of the femoral canal is performed with two different reaming devices Procedure: Chirurgical procedure Pulmonary Active, Complications; NR Organ Failure; Systemic Inflammatory Response Syndrome 36 Tibia or Femur Pseudo-arthrosis Susp 50 Adt Amputation; Phantom Limb; Stump Pain Comp 7 Comp 12 Adt Oct-08 Dec-11 University of http://ClinicalTrials.gov/show/NCT00667264 Sen California, San Diego; Summit Medical; National Institute of General Medical Sciences (NIGMS) Adt Oct-11 Nov-11 Rigshospitalet, http://ClinicalTrials.gov/show/NCT01449097 Denmark Monly Osseous Setting Improvement With Co-implantation of Osseous Matrix and Mesenchymal Progenitors Cells From Autologous Bone Marrow Phase II: Single group assignment NCT00557635 Ambulatory Continuous Peripheral Procedure: Nerve Blocks for Treatment of perineural Post-Amputation Phantom Limb ropivacaine and Stump Pain RCT, efficacy study NCT00667264 Adductor-Canal-Blockade Versus the Femoral Nerve Block Effect on Muscle Strength and Mobilization in Healthy Volunteers Phase IV: RCT, efficacy study NCT01449097 Procedure: Adductor- Muscle Strength; Canal-Blockade; Healthy Volunteers Procedure: The femoral nerve block; Procedure: Placebo 343 Adt Oct-08 Dec-12 University of http://ClinicalTrials.gov/show/NCT00771862 Sen California, San Diego; National Institute of General Medical Sciences (NIGMS) Adt May-03 May-12 Ullevaal http://ClinicalTrials.gov/show/NCT01042132 University Hospital Jan-08 Dec-11 University Hospital, ClermontFerrand http://ClinicalTrials.gov/show/NCT00557635 Effects of Right Lower Limb Orthopedic Immobilization on Braking Function RCT NCT01171287 Trial of Nonsurgical Treatment of Intermittent Claudication Due to Femoro-Popliteal Disease RCT NCT00798850 Procedure: Driving Automobile Driving Active, with an Aircast With an Aircast NR Walker; Procedure: Walker; Automobile Driving with a Driving With a walking cast; Walking Cast Procedure: Driving with a running shoe Procedure: Femoropopliteal Active, Percutaneous Disease; Intermittent NR Transluminal Claudication Angioplasty (PTA); Procedure: Supervised Exercise Programme (SEP); Procedure: Combined Treatment Perineural Catheter Insertion Procedure: Sciatic Distance for Continuous Peripheral catheter left 0-1cm Nerve Blocks past needle tip vs. 5Phase IV: RCT, safety/efficacy 6cm past needle tip study NCT00997867 Other Treadmill Training With Lower Other: Treadmill Extremity Amputees Training Phase I: RCT, efficacy study NCT01419288 Use of Near Infrared Spectroscopy Other: Shaving to Detect Muscle Perfusion in the Lower Extremity of Uninjured Subjects Cross-sectional study NCT01284023 Assessment of Socket Shapes Other: Assessed for Made by Central Fabrication socket fit Facilities Prospective, cohort study NCT01245504 14 Adt Sep-08 Jul-11 Universitaire de http://ClinicalTrials.gov/show/NCT01171287 Sherbrooke; Fonds de la Recherche en Santé du Québec; BSN Medical Inc 178 Child Aug-02 Dec-10 University of http://ClinicalTrials.gov/show/NCT00798850 Adt Hull; Hull and Sen East Yorkshire Hospitals NHS Trust; British Journal of Surgery Research Grant; European Society of Vascular Surgery Research Grant 350 Adt Nov-09 Oct-10 University of http://ClinicalTrials.gov/show/NCT00997867 Sen California, San Diego Lower Extremity Surgery; Upper Extremity Surgery; Post-operative Pain Comp Traumatic Amputation of Lower Extremity Rec 20 Adt Jun-09 Jun-12 Stony Brook Sen University http://ClinicalTrials.gov/show/NCT01419288 Acute Compartment Syndrome Active, NR 42 Adt Jan-11 Jan-12 J&M Shuler; Sen Nonin Medical http://ClinicalTrials.gov/show/NCT01284023 People With Lower Limb Amputation That Are Ambulatory Rec 50 Adt Nov-08 Dec-11 University of Sen Washington http://ClinicalTrials.gov/show/NCT01245504 Fonly 344 A Comparison of External Mechanical Work Between Different Prosthetic Feet RCT NCT01340807 Segment Transport Versus Acute Shortening In The Treatment of Tibial Pseudarthroses With Bone Loss Non-randomized, parallel assignment, safety/efficacy study NCT01246934 Other: Specialized Traumatic Comp Functional Prosthetic Amputation of Lower Training Extremity 15 Other: Asr Method Comp 22 Child Oct-09 Feb-10 Bezmialem Vakif http://ClinicalTrials.gov/show/NCT01246934 Adt University Rec 30 Child Feb-11 Aug-14 Rambam Health http://ClinicalTrials.gov/show/NCT01255241 Adt Care Campus Miscellaneous observational studies The Effect of Lower Limb Deformities (LLD) on Children's Gait and on Energy Expenditure Prospective, case-only study NCT01255241 Longitudinal Study of Weight Change Following Lower Limb Amputation Retrospective, cohort study NCT00932399 The Use of Near Infrared Spectroscopy in the Diagnosis of Acute Compartment Syndrome in Trauma Patients Prospective, case control study NCT01547013 To Assess Rotation for Femoral Version and Tibial Torsion Cross-sectional, cohort study NCT01531296 Gait Stability of People With Lower-limb Amputations Prospective, case control study NCT00915109 Musculoskeletal Measurements in Transfemoral Amputees Cross-sectional, cohort study NCT00909922 Tibia Pseudoarthroses Lower Limbs Deformities; Gait; Energy Expenditure Amputation Anterior Tibial Compartment Syndrome Rotational Malalignment of the Lower Extremities Adt Mar-08 Jan-11 Miami VA Healthcare System http://ClinicalTrials.gov/show/NCT01340807 Active, 9000 Adt Mar-10 Jun-13 Department of http://ClinicalTrials.gov/show/NCT00932399 NR Sen Veterans Affairs Rec Monly 130 Adt Feb-12 Feb-13 U.S. Army Medical Research and Materiel Command http://ClinicalTrials.gov/show/NCT01547013 Invite 50 Child Oct-11 Nov-12 University of Adt Utah http://ClinicalTrials.gov/show/NCT01531296 Gait; Balance Rec 60 Adt Jun-09 Apr-12 Kim Parker Sen http://ClinicalTrials.gov/show/NCT00915109 Lower Limb Loss Rec 80 Adt Jan-06 Dec-10 Miami VA Sen Healthcare System http://ClinicalTrials.gov/show/NCT00909922 345 A12. GENERAL A12A: PAEDIATRIC Title Phases: trial design (control) CT ID Drugs including biologics Study to Evaluate the Safety of Kedbumin 25% Versus Normal Saline in the Treatment of PostSurgical Hypovolemia in Pediatric Patients Phase II/III: RCT, safety study NCT01531803 Safety and Efficacy of Palonosetron IV to Prevent Postoperative Nausea and Vomiting in Pediatric Patients Phase III: RCT, safety/efficacy study NCT01395901 Prevention of Post Operative Bone Loss in Children RCT, efficacy study NCT00655681 Interventions Conditions Drug: Kedbumin 25% Hypovolemia; elective cardiac, abdominal, orthopedic, or transplant surgery. Drug: Palonosetron; Postoperative Drug: Ondansetron Nausea and Vomiting Recruit n Age Start (Grp) Date Not yet Rec 60 Child Sep-12 Dec-13 Kedrion S.p.A. http://ClinicalTrials.gov/show/NCT01531803 660 Child Jun-11 May-12 Helsinn Healthcare SA http://ClinicalTrials.gov/show/NCT01395901 Rec Drug: pamidronate; Other: saline End Sponsors Date URL Osteoporosis; Comp 24 Child Sep-07 Aug-11 University of http://ClinicalTrials.gov/show/NCT00655681 Cerebral Palsy; Adt New Mexico; Spina Bifida; Thrasher Osteopenia; Research Fund Osteogenesis Imperfecta Measurement of the blood levels of Dyloject® as a single Undergoing routine Comp 25 Child Jun-10 Jun-11 Central http://www.controlledthe pain killer diclofenac in children intravenous bolus surgery including Manchester trials.com/ISRCTN65890744 following a single intravenous dose ear, nose and throat Foundation Trust Single group assignment, (ENT), orthopaedic, (CMFT) (UK) pharmacokinetics study urological and ISRCTN65890744 general RCT on Ketorolac and Tramadol in Drug: ketorolac; Fracture; Pain Not yet 120 Child Apr-09 Oct-10 IRCCS Burlo http://ClinicalTrials.gov/show/NCT00560443 Bone Fractures Pain of Child Drug: tramadol Rec Garofolo Phase IV: RCT, safety/efficacy study NCT00560443 346 Procedure The Treatment of Type I Open Fractures in Pediatrics Phase I/II: RCT, efficacy study NCT00870064 Other Outcomes of Orthopaedic Surgery Using Gait Laboratory Versus Observational Gait Analysis in Children With Cerebral Palsy Phase I/II: RCT, efficacy study NCT00419432 Procedure: Formal Fractures, Open Operative Treatment; Procedure: Emergency Department Treatment Rec 200 Child Mar-10 Mar-14 Children's Memorial Hospital Other: Routine Cerebral Palsy Observational Analysis (prior to procedure); Other: Routine Observational analysis supplemented with Gait Lab Information (prior to procedure) Rec 50 Child Jan-07 Oct-14 The Hospital for http://ClinicalTrials.gov/show/NCT00419432 Sick Children Phalanx of Active, Supernumerary Digit NR of Hand 50 Child Jul-11 Sep-14 University of Adt Utah http://ClinicalTrials.gov/show/NCT01409980 Venous Thromboembolism; Deep Venous Thrombosis; Pediatrics 25 Child May-09 Mar-10 Penn State Adt University http://ClinicalTrials.gov/show/NCT01140386 Miscellaneous observational studies Triphalangeal Thumbs in the Pediatric Population: Long Term Outcomes Following Surgical Intervention Cohort study NCT01409980 Prevalence and Risk Factors of Venous Thromboembolism in Hospitalized Pediatric Patients Retrospective, cohort study NCT01140386 Comp 347 http://ClinicalTrials.gov/show/NCT00870064 A12B: FRACTURE & INJURY Title Phases: trial design (control) CT ID Behavioural Bone Physiology & Mechanics in Osteomyoplasty Amputation Rehabilitation RCT, efficacy study NCT00271362 Device A Randomized Controlled Cost Study of Infuse BMP 2 vs Iliac Crest Autograft for Non Union of Long Bone Fractures Phase IV: RCT, safety/efficacy study NCT00856479 The Use of RIA to Harvest Bone Graft for Treatment of Non-unions and Fractures Single group assignment, efficacy study NCT00582439 Drugs including biologics Antibiotic Prophylaxis in Orthopaedic Traumatology RCT NCT00610987 Methadone Versus Morphine for Orthopedic Surgery Patients Phase IV: RCT, efficacy study NCT00892606 Role of Pregabalin in Treatment of Post-Op Pain in Fracture Patients RCT, efficacy study NCT00583869 Interventions Conditions Recruit n Term 95 Adt Jan-06 Dec-10 Department of http://ClinicalTrials.gov/show/NCT00271362 Sen Veterans Affairs Wdrwn 80 Adt Mar-09 Mar-13 Capital District http://ClinicalTrials.gov/show/NCT00856479 Sen Health Authority, Canada; Canadian Orthopaedic Trauma Society Device: ReamerIrrigator-Aspirator (RIA) Orthopaedic Trauma Active, Fractures and NonNR unions 21 Adt Jan-07 Dec-10 University of Alabama at Birmingham; Synthes Inc. http://ClinicalTrials.gov/show/NCT00582439 Drug: cefazolin; Drug: Placebo Fractures, Closed; Wounds and Injuries Rec 700 Adt Jan-08 Jan-13 University of Sen MissouriColumbia http://ClinicalTrials.gov/show/NCT00610987 Drug: Methadone; Drug: Morphine Fracture; Pain, Postoperative Rec 80 Adt Jan-09 Dec-11 University of Louisville http://ClinicalTrials.gov/show/NCT00892606 Active, NR 150 Adt May-07 Aug-11 University of Sen Alabama at Birmingham; Pfizer http://ClinicalTrials.gov/show/NCT00583869 Behavioral: Amputation; Amputation Fracture; rehabilitation Inflammation; exercise program; Osteoporosis Procedure: Osteomyoplasty vs. routine long posterior flap Device: Infuse Bone Non Union Morphogenic Protein Diaphyseal (BMP) 2; Procedure: Fractures iliac crest autograft Drug: Placebo; Drug: Post-operative Pain Pregabalin; Drug: Pregabalin 348 Age Start (Grp) Date End Sponsors Date URL Procedure Effectiveness of Adipose Tissue Derived Mesenchymal Stem Cells as Osteogenic Component in Composite Grafts Phase II: RCT, safety/efficacy study NCT01532076 Radiation Exposure Using Laser Guided Fluoroscopy in Various Orthopaedic Procedures RCT NCT00972647 Fluid Lavage of Open Wounds RCT NCT00788398 Vacuum Assisted Closure as a Treatment for Open Fractures RCT, efficacy study NCT00582361 Procedure: Osteoporotic Cellularized Fractures composite graft augmentation; Procedure: Acellular composite graft augmentation Procedure: Laser Fractures beam guidance Procedure: Saline Solution; Procedure: Soap solution; Procedure: Gravity Flow Irrigation; Procedure: Low Pressure Irrigation; Procedure: High Pressure Procedure: Standard Wound Dressing; Device: VAC Other Osteogenic Cell Viability in Bone Other: cell viability Graft Obtained Using the Reamer and osteogenic Irrigator Aspirator (RIA) System potential analysis Versus Iliac Crest Bone Graft Prospective, cohort study NCT00843973 Reamer Irrigator Aspirator (RIA) vs Other: RIA Autogenous Iliac Crest Bone Graft harvesting group; (AICBG) for the Treatment of Non- Other: AICBG unions harvesting group RCT, bio-equivalence study NCT01382485 Not yet 290 Rec Rec 50 Adt Feb-12 Oct-15 University http://ClinicalTrials.gov/show/NCT01532076 Sen Hospital, Basel, Switzerland Adt Aug-09 Jun-11 Loma Linda Sen University http://ClinicalTrials.gov/show/NCT00972647 2280 Child Jun-09 Dec-12 Greenville http://ClinicalTrials.gov/show/NCT00788398 Adt Hospital System Sen University Medical Center; McMaster University; Department of Defense Open Fracture Wounds Invite Orthopaedic Traumatic Open Fractures Comp 63 Adt Jun-01 Jan-10 University of http://ClinicalTrials.gov/show/NCT00582361 Sen Alabama at Birmingham; KCI USA, Inc. Rec 30 Adt Jun-08 Dec-11 University of Sen MissouriColumbia; AO North America 88 Adt Fractures, Closed Nonunion of Bone Not yet Graft; Fractures Non Rec Union 349 Jan-12 Jan-14 St. Michael's Hospital, Toronto http://ClinicalTrials.gov/show/NCT00843973 http://ClinicalTrials.gov/show/NCT01382485 Miscellaneous observational studies Prevention of Infection in Surgical Treatment of Closed Fractures: Comparative of Cefazolin vs Vancomycin Prospective, case control study NCT01029457 Smoking Cessation in Nonunion, Malunion, Osseous Infection Prospective, case-only study NCT00754299 Validation of Laboratory Test for Predicting Bone Tissue Regeneration Prospective, cohort study NCT01362413 Arginine and Nitric Oxide (NO) Early Prognostic Markers for Nonunion Development Prospective study NCT01070576 Closed Fractures Rec 600 Adt Feb-10 Feb-13 University of Sen Tennessee http://ClinicalTrials.gov/show/NCT01029457 Fracture Nonunion; Infection Wdrwn 60 Adt Oct-10 Oct-12 Penn State Sen University http://ClinicalTrials.gov/show/NCT00754299 Nonunion of Fracture [Pseudarthrosis], Site Unspecified; Long bones Fracture Healing; Atrophic Non Union Development; Hypertrophic Non Union Development Rec 30 Adt Jan-11 Dec-13 Istituto Sen Ortopedico Rizzoli http://ClinicalTrials.gov/show/NCT01362413 Rec 100 Adt Mar-10 Mar-12 Maastricht Sen University Medical Center http://ClinicalTrials.gov/show/NCT01070576 Recruit n A12C: OTHER Title Phases: trial design (control) CT ID Behavioural An online aftercare programme to improve vocational reintegration after inpatient medical rehabilitation RCT, efficacy study ISRCTN33957202 Interventions Conditions Internet-based Vocationally strained Active aftercare intervention patients in + inpatient psychosomatic, rehabilitation; orthopaedic and Inpatient rehabilation cardiovascular only rehabilitation 800 350 Age Start (Grp) Date End Sponsors Date Adt Nov-10 Oct-13 German Sen Statutory Pension Insurance (Germany) URL http://www.controlledtrials.com/ISRCTN33957202 Ability of Near Infrared Spectroscopy to Isolate Compartments of the Extremity Phase I: Cross-sectional study NCT01283451 Mind Body Therapy During Geriatric Rehabilitation Single group assignment NCT01074788 Device Evaluation of an Acellular Osteochondral Graft for Cartilage LEsions Pilot Trial Phase II: RCT, safety/efficacy study NCT01183637 Evaluation of the Cartilage Autograft Implantation System Treatment for Articular Cartilage Lesions Phase III: RCT, safety/efficacy study NCT01508442 Agili-C Bi-phasic Implant Performances Phase IV: Single group assignment, efficacy study NCT01471236 Comparison of Bioactive Glass and Beeta-Tricalcium Phosphate as Bone Graft Substitute Phase IV: RCT, safety/efficacy study NCT00841152 N/K Jun-11 J&M Shuler Behavioral: Muscle contraction Acute Compartment Syndrome Active, NR 63 Adt Sen http://ClinicalTrials.gov/show/NCT01283451 Behavioral: mind body therapy Patients Who Are in Active, Need of Short or NR Long Term Rehabilitation Due to Neurological Event (Mainly Stroke) or Post Orthopedic Surgery 30 Adt Nov-09 Nov-10 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT01074788 Device: Kensey Articular Cartilage Nash Corp. Cartilage Injury Repair Device; Procedure: Microfracture Active, NR 30 Adt Jun-10 Apr-16 Kensey Nash Sen Corporation http://ClinicalTrials.gov/show/NCT01183637 Device: Cartilage Articular Cartilage Autograft Lesions Implantation System (CAIS); Procedure: Microfracture Rec 12 Adt Apr-11 May-15 The Hawkins Foundation; DePuy Mitek http://ClinicalTrials.gov/show/NCT01508442 Device: Agili-C BiCartilage and phasic Implant; Ostheochondral Procedure: miniDefects arthrotomy or arthroscopy Device: Bioactive Bone Neoplasm glass granules (Bonalive); Device: Beeta-tricalcium phosphate (ChronOs); Procedure: Autograft; Procedure: Allograft (frozen femoral head) Rec 20 Adt Jun-11 Aug-14 Cartiheal (2009) http://ClinicalTrials.gov/show/NCT01471236 Ltd Rec 180 Adt Mar-09 Dec-13 Turku University http://ClinicalTrials.gov/show/NCT00841152 Sen Hospital 351 Sutures Versus Staples for Wound Device: Sutures; Closure in Orthopaedic Surgery Device: Staples RCT, efficacy study NCT01146236 Surgical Wound Infection Rec 2560 Adt Sen Jul-10 Dec-13 University of http://ClinicalTrials.gov/show/NCT01146236 Manitoba; Manitoba Institute for Patient Safety; Manitoba Medical Services Foundation; Alexander Gibson Fund Adt Mar-10 Sep-13 InSightec http://ClinicalTrials.gov/show/NCT01085565 Sen Focused Ultrasound Surgery in the Device: ExAblate Bone Cancer; Bone Rec 50 Treatment of Pain Resulting From 2100 Metastases; Pain Metastatic Bone Tumors With the ExAblate 2100 Conformal Bone System Phase II: Single group assignment, safety/efficacy study NCT01085565 Closure of Fasciotomy Wounds: A Device: DermaClose Wounds and Rec 20 Adt Jul-10 Prospective, Observational Study Continuous External Injuries; Sen of a Continuous External Tissue Tissue Expander; Compartment Expander Device: Vessel loop Syndrome Non-randomised, parallel assignment, efficacy study NCT01171534 ExAblate Conformal Bone System Device: ExAblate Bone Metastases Rec 50 Adt Sep-09 Treatment of Metastatic Bone 2100 Sen Tumors for the Palliation of Pain Phase I: Single group assignment, safety/efficacy study NCT00981578 Vascular CT Assessment of Device: Cone Beam Bone Tumors Rec 20 Child Nov-06 Structural Autograft and Allograft CT Scan Adt Healing Sen Prospective, cohort study NCT00594776 The Use of Near Infrared Device: Near infrared Acute Compartment Not yet 120 Child Sep-11 Spectroscopy in the Diagnosis of spectroscopy (NIRS) Syndrome Rec Adt Acute Compartment Syndrome Prospective, cohort study NCT01171638 352 Jul-13 University of MissouriColumbia; Wound Care Technologies, Inc. http://ClinicalTrials.gov/show/NCT01171534 Feb-13 InSightec http://ClinicalTrials.gov/show/NCT00981578 Jan-13 University of http://ClinicalTrials.gov/show/NCT00594776 Rochester; National Institutes of Health Dec-12 J&M Shuler; http://ClinicalTrials.gov/show/NCT01171638 Department of Defense; Nonin Medical Coiled Catheters for Regional Anesthesia RCT, efficacy study NCT01290185 Transcutaneous Electrical Nerve Stimulation (TENS) and Fibromyalgia (FM) RCT NCT00932360 Device: Placement of Arthritis different catheters for continuous nerve block Device: Transient Fibromyalgia Placebo TENS (Rehabilicare Maxima TENS); Device: Active TENS (Rehabilicare Maxima TENS); Device: No TENS (Rehabilicare Maxima TENS) Device: Window Pressure Ulcer A Multi-centre Evaluation of the Performance of Window Dressings on Subjects With High Risk Pressure Ulceration Phase IV: Single group assignment, efficacy study NCT01438541 ExAblate (Magnetic Resonance- Device: ExAblate Bone Metastases; guided Focused Ultrasound 2000; Device: Sham Multiple Myeloma Surgery) Treatment of Metastatic Bone Tumors for the Palliation of Pain Phase III: RCT, safety/efficacy study NCT00656305 Assessment of Near Infrared Device: near-infrared Compartment Spectroscopy as a Diagnostic Tool spectroscopy Syndrome in Acute Compartment Syndrome Prospective, cohort study NCT01077934 Hyaluronic Acid Injection Post Device: Hyaluronic Cartilage Injury Arthroscopy - Does it Improve Acid Injection; Drug: Immediate Function? Double Blind Saline Injection Controlled Prospective Study Phase I/II: RCT, safety/efficacy study NCT01442571 Rec 152 Adt Apr-11 Aug-12 Sunnybrook http://ClinicalTrials.gov/show/NCT01290185 Sen Health Sciences Centre Rec 50 Adt Jun-09 Jun-12 University of http://ClinicalTrials.gov/show/NCT00932360 Sen Iowa; Orthopedic Section of the American Physical Therapy Association Rec 26 Adt Sep-11 Feb-12 Molnlycke http://ClinicalTrials.gov/show/NCT01438541 Sen Health Care AB Rec 148 Adt Mar-08 Dec-11 InSightec Sen http://ClinicalTrials.gov/show/NCT00656305 Not yet 200 Child Nov-11 Oct-11 J&M Shuler; http://ClinicalTrials.gov/show/NCT01077934 Rec Adt Emory University Sen Not yet 100 Rec 353 Adt Aug-11 Hadassah Medical Organization http://ClinicalTrials.gov/show/NCT01442571 The Use of Near Infrared Spectroscopy in the Diagnosis of Acute Compartment Syndrome in Injured Soldiers Prospective, cohort study NCT01123798 Bioactive Glass Granules in Filling of Bone Defects Phase IV: RCT, efficacy study NCT01304121 Perioperative Temperature Management RCT, efficacy study NCT00617136 Ultrasound Visualization Versus Electrical Nerve Stimulation Phase IV: RCT, safety/efficacy study NCT01010412 Vagus Nerve Stimulation for Treating Adults With Severe Fibromyalgia Phase I: Single group assignment, safety/efficacy study NCT00294281 Device: near-infrared Acute Compartment spectroscopy Syndrome Comp 300 Adt Feb-10 Jan-11 J&M Shuler; Department of Defense; Somanetics Corporation Device: Bioactive glass (SP53P4) Comp 48 Adt Oct-06 Dec-10 Turku University http://ClinicalTrials.gov/show/NCT01304121 Sen Hospital Rec 279 Adt Apr-08 Dec-10 VU University Sen Medical Center http://ClinicalTrials.gov/show/NCT00617136 Rec 450 Adt Feb-09 Sep-10 Allentown Sen Anesthesia Associates; SonoSite, Inc. http://ClinicalTrials.gov/show/NCT01010412 Comp 14 Adt Bone Tumors Device: Hypothermia Intraoperative warming (Bair Hugger); Device: Pre- and intraoperative warming (HotDog); Device: Intraoperative warming (HotDog) Device: Ultrasound Trauma to the Arm, (Sonosite Titan TShoulder, Elbow, shaped ultrasound Forearm, or Hand probe); Device: Electrical Nerve Stimulation (Stimuplex (B Braun) needle) Device: Vagus Nerve Fibromyalgia Stimulation (VNS) Therapy 354 http://ClinicalTrials.gov/show/NCT01123798 Oct-06 Jun-10 University of http://ClinicalTrials.gov/show/NCT00294281 Medicine and Dentistry New Jersey; National Institute of Arthritis and Musculoskeletal and Skin Diseases; National Institute of Neurological Disorders and Stroke (NINDS) Dietary supplements Muscle Regrowth During Physical Rehabilitation and Amino Acid Supplementation RCT NCT00760383 Dietary Supplement: Osteoarthritis Essential amino acids; Dietary Supplement: Alanine Testing the Effect of Crustacean's Dietary Supplement: Skeletal Deformities; Gastrolith Nutraceutical on gastrolith calcium Leg Length Mineralization Rate During Discrepancy Distraction Osteogenesis Phase I: Non-randomized, single group assignement, safety/efficacy study NCT01087437 Drugs including biologics Neocartilage Implant Phase III Trial Phase III: RCT, efficacy study NCT01400607 A Study of Pre-Operative Treatment of Newly-Diagnosed, Surgically-Resectable Osteosarcoma With Doxorubicin, Ifosfamide, Etoposide, and Cisplatin With Early Metabolic Assessment of Response Single group assignment, safety/efficacy study NCT01258634 Randomized Controlled Trials of the Effects of Decadron on Swallowing, Airway, and Arthrodesis Phase I/II: RCT, safety/efficacy study NCT01065961 Rec 60 Rec Biological: Articular Cartilage Rec Neocartilage Disorder; Implant/DeNovo® ET Degeneration; (Engineered Tissue Articular Cartilage; Graft); Other: Chronic Cartilage Microfracture Injury; Acute Cartilage Injury; Defect of Articular Cartilage Drug: Dexrazoxane; Osteosarcoma; Lung Term Drug: Doxorubicin; Metastases Drug: Cisplatin; Drug: G-CSF; Drug: PEG-filgrastim; Drug: Etoposide; Drug: Ifosfamide; Drug: Mesna; Drug: Leucovorin 225 Drug: Decadron; Drug: Saline 200 Swallowing Rec 2 355 Adt Jun-08 Aug-13 Eunice Kennedy http://ClinicalTrials.gov/show/NCT00760383 Sen Shriver National Institute of Child Health and Human Development Child Jan-11 Dec-11 Hadassah http://ClinicalTrials.gov/show/NCT01087437 Adt Medical Organization; Amorfical Adt Jul-11 Jul-19 ISTO Technologies, Inc.; Zimmer, Inc. http://ClinicalTrials.gov/show/NCT01400607 Child Jul-10 May-18 University of Adt Chicago http://ClinicalTrials.gov/show/NCT01258634 Adt Nov-08 Nov-16 Albany Medical Sen College http://ClinicalTrials.gov/show/NCT01065961 Post Market Study of DeNovo NT, Natural Tissue Graft Prospective, case-only study NCT00791245 A Study to Determine the Activity of SCH 717454 in Subjects With Relapsed Osteosarcoma or Ewing's Sarcoma (Study P04720AM3) Phase II: RCT, efficacy study NCT00617890 Efficacy of Local Powder Prophylactics RCT, safety/efficacy study NCT01372371 Biological: Cartilage Repair Particulated Juvenile Cartilage Allograft Active, NR 25 Drug: SCH 717454 (19D12) Active, NR 249 Child Feb-08 Aug-13 Schering-Plough http://ClinicalTrials.gov/show/NCT00617890 Adt Sen Rec 1844 Child Jun-11 Jun-13 Ganga Hospital http://ClinicalTrials.gov/show/NCT01372371 Adt Sen Biological: Vancomycin; Biological: Vancomycin and Gentamycin; Biological: Cefuroxime Pre- Versus Post-incisional Drug: Pregabalin; Pregabalin for Postoperative Pain Drug: Pregabalin Attenuation and Analgesics Spare in Orthopedic Oncologic Patients RCT NCT01359059 Study of Melatonin on Sleep, Pain, Drug: Melatonin; and Delirium After Joint Drug: Placebo Replacement Surgery RCT, safety/efficacy study NCT01505465 NeoCart Phase 2 Clinical Trial Biological: NeoCart; Phase II: RCT, safety/efficacy Procedure: study microfracture NCT00548119 Osteosarcoma; Sarcoma, Ewing's; Peripheral Neuroectodermal Tumor Infection Postoperative Pain Adt Jan-06 Dec-13 Zimmer Orthobiologics, Inc. http://ClinicalTrials.gov/show/NCT00791245 Not yet Rec 80 Adt Jun-11 Jun-13 Tel-Aviv Sen Sourasky Medical Center Postoperative Pain; Not yet Delirium; Confusion; Rec Sleep 50 Adt Feb-12 Feb-13 Hospital for http://ClinicalTrials.gov/show/NCT01505465 Sen Special Surgery, New York Articular Cartilage Damage 30 Adt Dec-06 Jan-13 Histogenics Corporation Active, NR 356 http://ClinicalTrials.gov/show/NCT01359059 http://ClinicalTrials.gov/show/NCT00548119 Combination Chemotherapy Before and After Surgery in Treating Patients With Osteosarcoma Phase II NCT00019864 Biological: filgrastim; Cardiac Toxicity; Drug: cisplatin; Drug: Sarcoma dexrazoxane hydrochloride; Drug: doxorubicin hydrochloride; Drug: leucovorin calcium; Drug: methotrexate; Procedure: adjuvant therapy; Procedure: conventional surgery; Procedure: neoadjuvant therapy Acute Pain and Inflammation After Drug: 1 Ketorolac Acute Pain; Pain Surgery intraarticular; Drug: Relief Phase IV: RCT, Placebo pharmacokinetics/dynamics study NCT00774540 Treatment of Methicillin-sensitive Drug: association of Osteoarticular Staphylococcus Aureus (MSSA) RIFAMPIN + Infection RCT CLINDAMYCIN; NCT01500837 Drug: association of LEVOFLOXACIN+ CLINDAMYCIN Echo-Doppler Assessment of the Drug: Enoxaparin Deep Vein Occurrence of Asymptomatic DVT Thrombosis; in Orthopedic Replacement Enoxaparin; Surgery Under Enoxaparin Anticoagulants Phase IV: RCT, safety/efficacy study NCT01354704 Open Label Trial of NanoDOX Drug: NanoDOX Orthopedic Trauma Hydrogel in Orthopedic Trauma Hydrogel; Other: Wounds Wounds With and Without Vacuum VAC Alone Assisted Closure Therapy Phase II: RCT, safety/efficacy study NCT01518491 Active, NR 100 Child Mar-00 Dec-12 National Cancer http://ClinicalTrials.gov/show/NCT00019864 Adt Institute (NCI) Rec 40 Adt Aug-08 Dec-12 Oslo University Sen Hospital http://ClinicalTrials.gov/show/NCT00774540 Active, NR 23 Adt Oct-10 Dec-12 Assistance Sen Publique Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT01500837 Rec 240 Adt Mar-11 Dec-12 Les Laboratoires http://ClinicalTrials.gov/show/NCT01354704 Sen des Médicaments Stériles; Hospital Charles Nicolle Tunis. Not yet Rec 24 Adt Apr-12 Dec-12 Nanohttp://ClinicalTrials.gov/show/NCT01518491 Sen therapeutics, Inc.; Department of Defense 357 Biological: filgrastim; Sarcoma Active, 44 Adt Aug-01 Oct-12 City of Hope Drug: dexrazoxane NR Medical Center; hydrochloride; Drug: National Cancer doxorubicin Institute (NCI) hydrochloride; Drug: ifosfamide; Drug: irinotecan hydrochloride; Genetic: protein expression analysis; Other: immunoenzyme technique; Procedure: adjuvant therapy; Procedure: conventional surgery; Procedure: neoadjuvant therapy; Radiation: radiation therapy Lusedra (Fospropofol Disodium) Drug: Fospropofol Procedural Sedation; Susp 150 Adt Feb-11 Oct-12 Mayo Clinic; for Minimal to Moderate Sedation disodium; Drug: Regional Anesthesia Sen Eisai Inc. for Regional Anesthesia Block Fospropofol Block; Orthopedic Prior to Orthopedic Surgery disodium; Drug: Surgery Phase IV: RCT, efficacy study Placebo + NCT01195103 Midazolam Prevention of Surgical Site Drug: mupirocin Surgical Site Rec 3000 Adt Mar-11 Sep-12 3M Infection; hip, knee, Infections: Effectiveness of Nasal calcium ointment, Sen Povidone-Iodine and Nasal 2%; Drug: Povidone- shoulder and elbow arthroplasty surgery Mupirocin iodine solution 5% Phase IV: RCT w/w (0.5% available and primary spinal fusion surgery NCT01313182 iodine) Patient Preoperative Skin Preparation DVT Prophylaxis in Orthopaedic Drug: Dalteparin Bone Cancer Active, 70 Adt Jul-06 Jul-12 M.D. Anderson Oncology Patients - A Safety NR Sen Cancer Center; Study Pfizer Single group assignment, safety/efficacy study NCT00525057 Combination Chemotherapy and Dexrazoxane Followed by Surgery and Radiation Therapy in Treating Patients With Advanced Soft Tissue Sarcoma or Recurrent Bone Sarcoma Phase II NCT00544778 358 http://ClinicalTrials.gov/show/NCT00544778 http://ClinicalTrials.gov/show/NCT01195103 http://ClinicalTrials.gov/show/NCT01313182 http://ClinicalTrials.gov/show/NCT00525057 Phase II Dose-ranging Study of APD421 in PONV Phase II: RCT, safety/efficacy study NCT01510704 Surgical Surveillance Trial to Evaluate a Shortened Infusion Time of Intravenous Ibuprofen Phase IV: Single group assignment, safety/efficacy study NCT01334957 Double-Blinded Clinical Trial Using Apatone®B for Symptomatic Postoperative Total Joint Replacements Phase II: RCT, safety/efficacy study NCT01272830 Combination Chemotherapy in Treating Patients With Stage III or Stage IV Malignant Peripheral Nerve Sheath Tumors Phase II NCT00304083 Drug: APD421; Drug: Postoperative Placebo Nausea and Vomiting; elective surgery requiring overnight stay Drug: Intravenous Pain ibuprofen Rec 200 Adt Jan-12 Jun-12 Acacia Pharma http://ClinicalTrials.gov/show/NCT01510704 Sen Ltd Rec 300 Adt Jun-11 Jun-12 Cumberland http://ClinicalTrials.gov/show/NCT01334957 Sen Pharmaceuticals Drug: Placebo; Drug: Edematous; Apatone®B Synovitis; Foreign Body Reaction; Osteolysis Rec 60 Adt Oct-10 Jun-12 Summa Health http://ClinicalTrials.gov/show/NCT01272830 Sen System; Crystal Clinic Orthopaedic Center LLC 74 Child Dec-05 Apr-12 Sarcoma http://ClinicalTrials.gov/show/NCT00304083 Adt Alliance for Sen Research through Collaboration; National Cancer Institute (NCI) Biological: filgrastim; Neurofibromatosis Rec Drug: doxorubicin Type 1; Sarcoma hydrochloride; Drug: etoposide; Drug: ifosfamide; Procedure: conventional surgery; Radiation: radiation therapy Observation, Radiation Therapy, Drug: doxorubicin Childhood Malignant Active, Combination Chemotherapy, hydrochloride; Drug: Fibrous Histiocytoma NR and/or Surgery in Treating Young ifosfamide; Other: of Bone; Sarcoma Patients With Soft Tissue Sarcoma clinical observation; Phase III Procedure: NCT00346164 therapeutic conventional surgery; Radiation: radiation therapy Rosuvastatin for Preventing Deep Drug: Rosuvastatin Deep Vein Rec Vein Thrombosis 20mg/d for 14days; Thrombosis; Phase IV: RCT, safety/efficacy Drug: enoxaparin Venous; study only Thrombosis; NCT01021488 Prevention 600 Child Feb-07 Mar-12 Children's http://ClinicalTrials.gov/show/NCT00346164 Adt Oncology Group; National Cancer Institute (NCI) 180 359 Adt Oct-09 Mar-12 Hallym Sen University Medical Center http://ClinicalTrials.gov/show/NCT01021488 How Lidocaine Affects Outcomes In Orthopedic Surgery Patients Phase IV: RCT, efficacy study NCT01179100 Traumeel S for Reduction of Post Operative Pain Following Arthroscopy Phase III: RCT, efficacy study NCT00307892 Oral Versus Intravenous Antibiotics for Bone and Joint Infections (OVIVA B&J) Phase IV: RCT, safety/efficacy study NCT00974493 Drug: Lidocaine Orthopedic; Surgery; Invite Elderly 100 Adt Jun-11 Feb-12 Cedars-Sinai Sen Medical Center http://ClinicalTrials.gov/show/NCT01179100 Drug: Traumeel S: intra-operative irrigation + oral ingestion; Drug: Placebo Drug: Antibiotics Post-operative Pain Susp 98 Adt Jan-11 Jan-12 Shaare Zedek Medical Center http://ClinicalTrials.gov/show/NCT00307892 Bone Infection; Joint Infection Invite 200 Clinical Study to Investigate the Efficacy and the Safety of Dexmedetomidine in Sedation During the Surgery With Epidural Anesthesia or Spinal Anesthesia Without Intubation Phase III: RCT, safety/efficacy study NCT01438957 Pregabalin in the Prevention of Postoperative Delirium and Pain Phase III: RCT, safety/efficacy study NCT00819988 Preoperative Thalidomide With Radiation Therapy For Patients With Low-Grade Primary Soft Tissue Sarcoma or Thalidomide With Radiation Therapy and Chemotherapy For Patients With High-Grade or Intermediate-Grade Primary Soft Tissue Sarcoma of the Arm, Leg, or Body Wall Phase II NCT00089544 Drug: Dexmedetomidine hydrochloride Sedation Rec 120 Adt Jun-10 Nov-11 Oxford http://ClinicalTrials.gov/show/NCT00974493 Sen University Hospitals NHS Trust; Nuffield Orthopaedic Centre NHS Trust Adt Jun-11 Nov-11 Hospira, Inc.; http://ClinicalTrials.gov/show/NCT01438957 Sen Maruishi Pharmaceutical Drug: Pregabalin; Other: Sugar pill Delirium; Pain Comp 240 Adt May-09 Oct-11 Ottawa Hospital http://ClinicalTrials.gov/show/NCT00819988 Sen Research Institute; Pfizer Comp 44 Child Jun-04 Sep-11 Radiation http://ClinicalTrials.gov/show/NCT00089544 Adt Therapy Sen Oncology Group; National Cancer Institute (NCI) Biological: filgrastim; Sarcoma Drug: dacarbazine; Drug: doxorubicin hydrochloride; Drug: ifosfamide; Drug: thalidomide; Procedure: adjuvant therapy; Procedure: conventional surgery; Procedure: neoadjuvant therapy; Radiation: radiation therapy 360 Supporting the Health of Adults Drug: donepezil; Delirium Active, 40 Sen Jan-07 Aug-11 Beth Israel http://ClinicalTrials.gov/show/NCT00586196 Undergoing Orthopedic Surgery Drug: Placebo NR Deaconess During the Recovery Period Medical Center; Phase II: RCT, safety study National Institute NCT00586196 on Aging (NIA) Safety and Efficacy of Repeated Drug: PMI-150 Pain, Postoperative Comp 250 Adt Jun-08 Aug-11 Hospira, Inc. http://ClinicalTrials.gov/show/NCT00709436 Doses of PMI-150 (Intranasal (intranasal Sen Ketamine) in Acute Post-operative ketamine); Drug: Pain Following Orthopedic Surgery Placebo Phase III: RCT, safety/efficacy study NCT00709436 Combination Chemotherapy, PEG- Biological: PEGSarcoma Rec 2300 Child Nov-05 Jun-11 Children's http://ClinicalTrials.gov/show/NCT00134030 Interferon Alfa-2b, and Surgery in interferon alfa-2b; Adt Oncology Group; Treating Patients With Drug: cisplatin; Drug: National Cancer Osteosarcoma doxorubicin Institute (NCI); Phase III: RCT hydrochloride; Drug: University NCT00134030 etoposide; Drug: College London ifosfamide; Drug: Hospitals methotrexate Cognitive Effects of Inhalational Drug: inhalation Lumbar Spondylosis; Rec 200 Sen Nov-08 Jun-11 Duke University; http://ClinicalTrials.gov/show/NCT00788008 Versus Intravenous General anesthesia with Cervical Department of Anesthesia in the Elderly isoflurane vs. TIVA Spondylosis; Hip Veterans Affairs RCT, pharmacodynamics study with propofol Osteoarthritis; Knee NCT00788008 Osteoarthritis Assessing the Role of “Statin” Drug: simvastatin; Perioperative Rec 70 Adt Apr-08 Jun-11 Mayo Clinic http://ClinicalTrials.gov/show/NCT00656292 Therapy and Perioperative Drug: placebo Inflammatory Sen Inflammatory Response in Patients Response Undergoing Major Orthopedic Surgery" Phase IV: RCT, efficacy study NCT00656292 Chlorhexidine Versus Betadine in Drug: Skin antisepsis Infection Not yet 200 Adt Oct-10 May-11 North Shore http://ClinicalTrials.gov/show/NCT00896402 Preventing Colonization of with chlorhexidine; Rec Sen Long Island Femoral Nerve Catheters After Drug: povidoneJewish Health Total Joint Arthroplasty (TJA) iodine System RCT, efficacy study NCT00896402 361 An Observational Study On The Drug: Fragmin® Venous Safety And Tolerability Of (Dalteparin Sodium) Thromboembolism Prolonged Thrombosis Prophylaxis With Fragmin® Prospective, cohort study NCT01046903 Prospective randomised singleGenta-Coll resorb® Acute and chronic blind trial for application of osteomyelitis GENTA-COLL resorb® for treatment of acute and chronic osteomyelitis RCT ISRCTN74677374 Treatment of Patients Colonized Drug: Placebo; Drug: Orthopedic With Methicillin-Resistant Altabax (retapamulin) Procedures; Staphylococcus Aureus Prior to Methicillin-resistant Bone and Joint Surgery Staphylococcus Phase II: RCT, efficacy study Aureus NCT00903279 Trial of 6% HES130/0.4 Drug: 6% Hypovolemia; Phase III: RCT, safety/efficacy hydroxyethyl starch Hemorrhage study 130/0.4; Drug: 6% NCT01010022 hydroxyethyl starch 70/0.5 (Salinhes®) The Effect of Combined Ephedrine Drug: Ephedrine Pain Due to Propofol and Lidocaine Pretreatment on 30microgram/kg; Injection; Pain and Hemodynamic Changes Drug: Hemodynamic Due to Propofol Injection lidocaine0.5mg/kg - Changes Due to Phase I/II: RCT, safety/efficacy ephedrine30 Propofol Injection study micrograms/kg; NCT01186549 Drug: ephedrine 70 microgram/kg; Drug: lidocaine 0.5mg/kg; Drug: normal saline 2ml Comp 503 Wtdrwn 320 Adt Mar-10 Feb-11 Pfizer Sen http://ClinicalTrials.gov/show/NCT01046903 Adt Feb-08 Feb-11 Friedrich Schiller http://www.controlledSen University Jena trials.com/ISRCTN74677374 (Germany) Wdrwn 400 Child Aug-09 Dec-10 Bay Pines VA Adt Healthcare Sen System http://ClinicalTrials.gov/show/NCT00903279 Comp 64 Adt Nov-09 Nov-10 Fresenius Kabi Sen Japan http://ClinicalTrials.gov/show/NCT01010022 Comp 165 Adt Aug-10 Nov-10 Qazvin University Of Medical Sciences http://ClinicalTrials.gov/show/NCT01186549 362 Sorafenib and Ifosfamide in Drug: sorafenib; Treating Patients With High-Grade Drug: Ifosfamide Soft Tissue Sarcoma or Bone Sarcoma That Can Be Removed by Surgery Phase II: Single group assignment, safety/efficacy study NCT00880542 The cerebrospinal fluid (CSF) Dyloject® (75 mg) pharmacokinetics of a single pre- single intravenous operative intravenous bolus dose bolus; Voltarol® of diclofenac (Dyloject®) in ampoules (75 mg) comparison to diclofenac infusion single intravenous (Voltarol®) infusion Phase IV: RCT ISRCTN37500282 Ultrasound Guided Supraclavicular Drug: Ropivacaine; Nerve Block Drug: Mepivacaine Phase III: RCT, safety/efficacy and ropivacaine study NCT00825786 Inhaled Sargramostim in Treating Biological: Patients With First Pulmonary sargramostim; (Lung) Recurrence of Procedure: Osteosarcoma conventional surgery Phase II NCT00066365 Prolotherapy Versus Steroids for Drug: Prolotherapy Thumb Carpo-metacarpal Joint (10% dextrose Arthritis solution); Drug: RCT, safety/efficacy study Corticosteroid NCT00685880 solution Sarcoma Term 7 Adt Aug-08 Nov-10 University of http://ClinicalTrials.gov/show/NCT00880542 Sen California, Los Angeles; National Cancer Institute (NCI) Undergo surgery performed under spinal anaesthesia Comp 20 Adt Feb-09 Aug-10 Barts and The London NHS Trust (UK) http://www.controlledtrials.com/ISRCTN37500282 Local Anesthetic; upper extremity procedures Comp 120 Adt Sep-08 Aug-10 Outcomes Sen Research Consortium http://ClinicalTrials.gov/show/NCT00825786 Metastatic Cancer; Sarcoma Comp 40 Child Jul-04 Adt Thumb Carpometacarpal Joint Osteoarthritis Term 2 Adt May-08 Jul-10 Mayo Clinic Sen 363 Jul-10 Children's http://ClinicalTrials.gov/show/NCT00066365 Oncology Group; National Cancer Institute (NCI) http://ClinicalTrials.gov/show/NCT00685880 Biological: filgrastim; Sarcoma Comp Drug: dacarbazine; Drug: doxorubicin hydrochloride; Drug: ifosfamide; Drug: mesna; Procedure: conventional surgery; Radiation: brachytherapy; Radiation: intraoperative radiation therapy; Radiation: radioisotope therapy Study of Daptomycin in Subjects Drug: daptomycin; Osteomyelitis Comp Undergoing Surgery for Drug: daptomycin; Osteomyelitis Associated With an Drug: vancomycin; Infected Prosthetic Caused by Drug: teicoplanin; Staphylococci Drug: nafcillin; Drug: Phase II: RCT, safety/efficacy oxacillin; Drug: study flucloxacillin NCT00428844 Ifosfamide and Doxorubicin, Drug: doxorubicin Childhood Malignant Rec Radiation Therapy, and/or Surgery hydrochloride; Drug: Fibrous Histiocytoma in Treating Young Patients With ifosfamide; of Bone; Sarcoma Localized Soft Tissue Sarcoma Procedure: adjuvant Phase III: Non-Randomized; therapy; Procedure: NCT00334854 conventional surgery; Procedure: neoadjuvant therapy; Radiation: radiation therapy Adt Feb-97 Jun-10 Radiation http://ClinicalTrials.gov/show/NCT00002791 Sen Therapy Oncology Group; National Cancer Institute (NCI); Eastern Cooperative Oncology Group Chemotherapy Plus Radiation Therapy Followed by Surgery in Treating Patients With Soft Tissue Sarcoma Phase II NCT00002791 75 Adt Jan-07 Jun-10 Cubist http://ClinicalTrials.gov/show/NCT00428844 Sen Pharmaceuticals 250 Child Mar-06 May-10 European http://ClinicalTrials.gov/show/NCT00334854 Adt Paediatric Soft Tissue Sarcoma Study Group; Italian Association for Pediatric Hematology Oncology; Cooperative Weichteilsarkom Studie; Children's Cancer and Leukaemia Group; Dutch Childhood Oncology Group 364 To compare dose and concentration of local anaesthetics in regional anaesthesia RCT ISRCTN44947124 To compare analgesia and side effects of intrathecal fentanyl and intrathecal morphine RCT, efficacy study ISRCTN49793641 Onset Time of Thiopental Versus Propofol in the Elderly Phase IV: RCT, efficacy study NCT00965107 20ml levobupivacaine 02.5% + 20ml lidocaine 1% for each block; 20ml levobupivacaine 02.5% + 20ml lidocaine 1% for femoral block AND 10ml levobupivacaine 0.5% + 10ml lidocaine 2% for sciatic block. 2.5ml heavy bupivacaine 0.5% + 25mcg fentanyl intrathecally; 2.5ml heavy bupivacaine 0.5% + 50 mcg morphine intrathecally; 2.5ml heavy bupivacaine 0.5% + 100mcg morphine intrathecally. Drug: Thiopental; Drug: Propofol Elective orthopaedic surgery Comp 40 Adt May-09 Apr-10 North Wales http://www.controlledSen NHS Trust (UK) trials.com/ISRCTN44947124 Elective orthopaedic surgery Comp 90 Adt May-09 Apr-10 North Wales http://www.controlledSen NHS Trust (UK) trials.com/ISRCTN49793641 Induction of Anaesthesia; Age Comp 78 Adt Sep-09 Mar-10 Rigshospitalet, Sen Denmark; TrygFonden, Denmark 365 http://ClinicalTrials.gov/show/NCT00965107 Biological: Sarcoma Active, dactinomycin; Drug: NR cyclophosphamide; Drug: doxorubicin hydrochloride; Drug: etoposide; Drug: ifosfamide; Drug: mesna; Drug: vincristine sulfate; Procedure: conventional surgery; Radiation: low-LET cobalt-60 gamma ray therapy; Radiation: low-LET photon therapy Intravenous Ferric Carboxymaltose Drug: Ferinject ® Iron Deficiency Rec (Ferinject®) With or Without Anemia Erythropoietin in Patients Undergoing Orthopaedic Surgery Phase IV: RCT, safety/efficacy study NCT00706667 Pharmacokinetic, Drug: intravenous Orthopaedic Surgery Rec Pharmacodynamic and morphine titration Pharmacogenetic of Morphine After Surgery Cross-sectional study NCT00822549 Child Jul-92 Jan-10 Klinik und http://ClinicalTrials.gov/show/NCT00002516 Adt Poliklinik fuer Kinder und Jugendmedizin Universitaetsklini kum Muenster; Medical Research Council Combination Chemotherapy Plus Surgery and Radiation Therapy in Treating Patients With Ewing's Sarcoma Phase III NCT00002516 Procedure Chondrofix Osteochondral Allograft Procedure: Prospective Study Chondrofix Phase IV: Single group Osteochondral assignment, efficacy study Allograft NCT01410136 Articular Cartilage Disorder; Degeneration; Articular Cartilage; Chronic Cartilage Injury; Acute Cartilage Injury; Defect of Articular Cartilage Rec 75 Adt May-08 Jan-10 University of http://ClinicalTrials.gov/show/NCT00706667 Sen Zurich; Vifor Inc. 500 Adt Sep-06 Jan-10 Assistance Sen Publique Hôpitaux de Paris http://ClinicalTrials.gov/show/NCT00822549 50 Adt Apr-11 Sep-17 Zimmer Sen Orthobiologics, Inc. http://ClinicalTrials.gov/show/NCT01410136 366 Prophylactic Antibiotic Regimens in Tumor Surgery (PARITY): Pilot Study Phase III: RCT, efficacy study NCT01479283 Optimizing Catheter Insertion Technique for Ultrasound-guided Continuous Peripheral Nerve Blocks RCT, efficacy study NCT01459523 Procedure: Prophylactic Cefazolin Antibiotic Regimen Infection; Bone Neoplasms Procedure: Proximal Pain, Postoperative placement; Procedure: Short axis ultrasound; Procedure: Long axis; Procedure: Distal placement Safety and Efficacy of Cryoablation Procedure: Pain; Neoplasm Combined With Radiation Therapy Cryoablation; Metastasis for the Palliation of Painful Bone Procedure: Radiation Metastases Phase I/II: Single group assignment, safety/efficacy study NCT01461252 Safety and Efficacy of Cryoablation Procedure: Pain; Neoplasm for the Palliation of Painful Bone Cryoablation Metastasis Metastases Phase I/II: Single group assignment, safety/efficacy study NCT01461265 Supported Fast track multi-Trauma Fast track multiMulti-trauma Rehabilitation Service trauma rehabilitation Non-randomized efficacy study service; ISRCTN68246661 Conventional multitrauma care service Can the Usage of Regional Block Procedure: regional Anesthesia; Time Room Save the Time of anesthesia Anesthesia Team Prospective, cohort study NCT01499589 Not yet 100 Child Jul-12 Jun-14 Michelle Ghert Rec Adt Sen http://ClinicalTrials.gov/show/NCT01479283 Rec 200 Adt Oct-11 Oct-13 VA Palo Alto Sen Health Care System http://ClinicalTrials.gov/show/NCT01459523 Not yet Rec 40 Adt Feb-12 Sep-13 Galil Medical Sen http://ClinicalTrials.gov/show/NCT01461252 Rec 40 Adt Nov-11 Jun-13 Galil Medical Sen http://ClinicalTrials.gov/show/NCT01461265 Active 164 Adt Oct-08 Dec-12 Adelante Sen Rehabilitation Centre (The Netherlands) http://www.controlledtrials.com/ISRCTN68246661 Rec 800 Child Oct-11 Jul-12 Mahidol Adt University Sen 367 http://ClinicalTrials.gov/show/NCT01499589 Postoperative Nausea/Vomiting and Acupressure Phase II: Non-randomised, parallel assignment, efficacy study NCT01389570 Procedure: Acupressure wrist band PET Scan Combined With CT Scan in Evaluating Treatment Response in Patients Undergoing Treatment for Bone Cancer or Soft Tissue Sarcoma Single group assignment NCT00335751 Procedure: Sarcoma computed tomography; Procedure: positron emission tomography; Procedure: radionuclide imaging; Radiation: fludeoxyglucose F 18 Radiotherapy with Extremity soft tissue Clinical Target sarcoma Volume (CTV) giving 5 cm margin; CTV volume giving a 1.5 cm margin longitudinally and 2 cm laterally Procedure: Osteoarticular Infections; including Microbiological prosthetic joint cultures and infection Molecular biology Procedure: Bone Tumors Navigation surgery; Procedure: Navigation system Randomised trial of volume of post-operative radiotherapy given to adult patients with extremity soft tissue sarcoma RCT ISRCTN76456502 Postoperative Nausea Not yet 2000 Child Sep-11 Jun-12 National http://ClinicalTrials.gov/show/NCT01389570 Rec Adt Research Centre Sen of Complementary and Alternative Medicine, Norway; Lovisenberg Diakonale Hospital Comp 120 Adt Jan-06 Oct-11 University of http://ClinicalTrials.gov/show/NCT00335751 Sen California, Los Angeles; National Cancer Institute (NCI) Comp Molecular Microbiology in OsteoRec arthritis Infection Prospective, case control study NCT01193803 Navigation Surgery for Bone and Rec Soft Tissue Tumor Single group assignment, safety study NCT01179698 Vacuum Assisted Closure as a Procedure: Standard Draining Hematoma Active, Treatment for Draining Pressure Dressing; NR Hematomas Device: VAC RCT, efficacy study NCT00582179 400 Child Jan-06 Jul-11 University of Adt Sheffield (UK) Sen http://www.controlledtrials.com/ISRCTN76456502/ 284 Adt Oct-08 Apr-11 Assistance Sen Publique Hôpitaux de Paris Child Jan-09 Dec-10 Samsung Adt Medical Center Sen http://ClinicalTrials.gov/show/NCT01193803 Adt Sep-01 Dec-10 University of Sen Alabama at Birmingham http://ClinicalTrials.gov/show/NCT00582179 45 94 368 http://ClinicalTrials.gov/show/NCT01179698 Pre and Post Arthrogram Ultrasound Images of Joints Single group assignment NCT00724659 HLA Sensitization Following Major Cortical Allograft Bone Procedures Phase IV: Prospective, caseonly study NCT00160719 Treatment Outcome After Surgical Treatment of Osteoid Osteoma Retrospective, cohort study NCT01466010 Other Observation Versus Post-surgery Radiotherapy After Complete Exeresis in Soft Tissues Members Sarcoma Phase III: RCT, efficacy study NCT00870701 Improving a Bayesian Model's Survival Estimates in Patients Needing Surgery for Bone Metastases Prospective, cohort study NCT01470105 Patient Anxiety and Concern as Predictors for the Perceived Quality and Efficacy of Treatment Prospective, cohort study NCT01205295 Procedure: Ultrasound; Procedure: Ultrasound Procedure: retrieve blood samples Arthrography Active, NR 300 Adt Sep-04 Sep-10 University of Sen Michigan http://ClinicalTrials.gov/show/NCT00724659 Bone Cancer Comp 120 Child Sep-99 Mar-10 University of Adt Florida Sen http://ClinicalTrials.gov/show/NCT00160719 Procedure: surgical removal of osteoid osteoma Osteoid Osteoma Comp 150 Child Jan-98 Jan-10 Universitaire Adt Ziekenhuizen Sen Leuven http://ClinicalTrials.gov/show/NCT01466010 Radiation: Soft Tissue Sarcoma Radiotherapy; Other: of Members absence of radiotherapy Rec 570 Adt Mar-09 Mar-21 Institut Claudius http://ClinicalTrials.gov/show/NCT00870701 Sen Regaud Other: blood Bone Metastases sampling, the SF-36 questionnaire Rec 440 Adt Nov-11 Nov-14 Memorial Sloan- http://ClinicalTrials.gov/show/NCT01470105 Sen Kettering Cancer Center; Naval Medical Research Center Other: Cognitive Anxiety; Orthopedic behavioural therapy Surgery Rec 800 Not yet Rec 10 Adt Sep-10 Feb-13 Kolding Sen Sygehus; Odense University Hospital; University of Southern Denmark Adt Jan-12 Jan-13 Tel-Aviv Sen Sourasky Medical Center Restrictive Versus Liberal Red Cell Other: Red blood Transfusion Strategy in cells transfusion Orthopedic-Oncology Patients Undergoing Surgery - a Randomized Controlled Study RCT NCT01491308 Red Blood Cells Transfusion. 369 http://ClinicalTrials.gov/show/NCT01205295 http://ClinicalTrials.gov/show/NCT01491308 Remote Orthopedic Outpatient Consultation by Help of Telemedicine RCT, safety/efficacy study NCT00616837 Pain and Function After Orthopedic Surgery Prospective, cohort study NCT01390298 A Migration and Bone Density Study Comparing 2 Types of Bone Cement in the OptiPac Bone Cement Mixing System RCT, safety/efficacy study NCT00678236 Dynamic Contrast Enhanced MRI(DCE-MRI)of Bone Tumors Single group assignment, efficacy study NCT00598741 Other: Telemedicine Orthopedic consultation Conditions Rec 400 Child Nov-07 Dec-12 University http://ClinicalTrials.gov/show/NCT00616837 Adt Hospital of North Sen Norway; Helse Nord Other: Observational Chronic Pain Rec 75 Adt Sen Sen Jun-08 Sep-12 University of http://ClinicalTrials.gov/show/NCT00678236 Aarhus; Aarhus University Hospital; Biomet, Inc. Jul-11 Nov-12 Wake Forest University Other: Refobacin Bone Cement R; Other: Refobacin Plus Bone Cement Osteoarthritis Active, NR 54 Other: DCE-MRI Sarcoma; Bone Tumor Active, NR 210 Child Jul-04 Adt Sen Tissue Sample Collection From Genetic: microarray Sarcoma Patients With Soft Tissue Sarcoma analysis; Genetic: of the Arms, Hands, Legs, or Feet molecular diagnostic Treated on Clinial Trial CRUKmethod; Other: VORTEX biologic sample NCT00900211 preservation procedure Orthopaedic Patient Recognition of Other: Orthopaedic Patient Satisfaction Attending Improves Satisfaction Attending Biosketch Evaluations (Orthopaedic PRAISE Card Study) RCT NCT01263639 Rec http://ClinicalTrials.gov/show/NCT01390298 Jul-12 Memorial Sloan- http://ClinicalTrials.gov/show/NCT00598741 Kettering Cancer Center; New York Presbyterian Hospital; University of Oregon; University College, London; Montefiore Hospital 400 Child Aug-07 Mar-12 Christie Hospital http://ClinicalTrials.gov/show/NCT00900211 Adt NHS Foundation Sen Trust Not yet 200 Rec 370 Adt Jan-11 Feb-12 Vanderbilt Sen University http://ClinicalTrials.gov/show/NCT01263639 Detection of Circulating Other: Blood draw Osteosarcoma Osteosarcoma Tumor Cells in the Blood of Patients Using the Polymerase Chain Reaction Prospective, cohort study NCT00588510 Amputee Residual Limb Volume Other: Monitored for Amputation Fluctuation limb volume Prospective, cohort study NCT01161238 Traditional Chinese Medicine in Routine care of Orthopaedic Rehabilitation - sustainability and acceptance by patients of the German Pension Fund RCT ISRCTN40932605 Comp Rec Usual care; usual Chronic back pain Comp care + TCM and/or osteoarthritis (acupuncture, tuina- of one or more joints massage, herbal therapy, qi gong or tai chi and consultations to way of life and dietetics) Establishment of Optimal Other: Allowed drop Anemia; Comp Transfusion Threshold After Major in hemoglobin to 4.5- Arthroplasty; Orthopedic Surgery 5.5 mmol/L; Other: Replacement; Hip RCT, efficacy study Allowed drop in NCT00906295 hemoglobin to level between 5.6-6.5 mmol/L Two Strategies for MethicillinOther: Rapid MRSA Infection Active, resistant Staphylococcus Aureus molecular MRSA NR (MRSA) Infection Prevention in test; Behavioral: Surgical Patients Hand hygiene Non-randomized, parallel promotion assignment NCT00685867 59 Child Jan-00 Sep-11 Memorial Sloan- http://ClinicalTrials.gov/show/NCT00588510 Adt Kettering Cancer Sen Center 100 Child May-10 Sep-11 University of http://ClinicalTrials.gov/show/NCT01161238 Adt Washington; Sen Eunice Kennedy Shriver National Institute of Child Health and Human Development 520 Adt Jan-09 Jun-11 Refonet http://www.controlledSen (Germany) trials.com/ISRCTN40932605 67 Adt Jun-09 Jun-11 Rigshospitalet, Sen Denmark; TrygFonden, Denmark http://ClinicalTrials.gov/show/NCT00906295 30 Child May-08 Dec-10 University Adt Hospital, Sen Geneva http://ClinicalTrials.gov/show/NCT00685867 371 Intensity-Modulated Radiation Therapy in Treating Patients Undergoing Surgery for Stage IB, Stage II, or Stage III Soft Tissue Sarcoma Phase II NCT00740597 Effect of Systematic Medication Review in Elderly Patients Admitted to an Orthopedic Department RCT, safety study NCT00738816 Genetic: gene Sarcoma expression analysis; Genetic: polymerase chain reaction; Genetic: western blotting; Procedure: neoadjuvant therapy; Procedure: therapeutic conventional surgery; Radiation: intensitymodulated radiation therapy Other: Systematic Elderly medication review and advisory notes Miscellaneous observational studies Retrieval and Analysis of Orthopedic Implants at Revision Arthroplasty Surgery Prospective, case-only study NCT01425021 Clinical Orthopaedic Data Bank (Acute and Chronic) Prospective study NCT00411060 Huntsman Biopsy Study Prospective, case-only study NCT00615329 Identification of Risk Factors of Prolonged Wound Healing Following Primary Arthroplasty Prospective, cohort study NCT01477047 Term 30 Adt Sen Comp 108 Adt Apr-09 Apr-10 Aarhus Sen University Hospital http://ClinicalTrials.gov/show/NCT00738816 Total Joint Revisions Invite 500 Adt Aug-10 Aug-20 University of Sen Utah http://ClinicalTrials.gov/show/NCT01425021 Osteoarthritis; Osteosarcoma; Scoliosis; Cerebral Palsy Soft Tissue Sarcoma; Osteosarcoma 1000 Child Jan-07 Jan-20 University of 0 Adt Florida Sen http://ClinicalTrials.gov/show/NCT00411060 Evaluate Surgical, Medical and Pharmacological Factors Influence on Wound Healing Following Primary Arthroplasty Surgery Rec Rec Jul-08 Apr-10 City of Hope http://ClinicalTrials.gov/show/NCT00740597 Medical Center; National Cancer Institute (NCI) 100 Child Apr-03 Dec-15 State University http://ClinicalTrials.gov/show/NCT00615329 Adt of New York Sen Upstate Medical University; Huntsman Cancer Institute Not yet 3000 Adt Jan-12 Jan-14 Hvidovre http://ClinicalTrials.gov/show/NCT01477047 Rec Sen University Hospital 372 Pro Osteon Bone Void Filler Study Prospective, cohort study NCT00858598 Prevention of Venous Thromboembolic Events After Elective Orthopaedic Surgery in Patients Treated With PRADAXA Prospective, cohort study NCT01139658 Effect of Spinal Cord Stimulation on Pain Thresholds and Sensory Perception in Chronic Pain Patients Cross-sectional, case-only study NCT01137617 Objective Functional Outcome Measures in Orthopedic Surgery Using Advanced Tracking Technologies Cross-sectional, cohort study NCT00641823 OrthoIllustrated Web Based Orthopaedic Sports Medicine Registry Prospective, cohort study NCT01191151 Musculotendinous Tissue Repair Unit and Reinforcement (MTURR) Prospective, cohort study NCT01292876 Musculotendinous Tissue Unit Repair and Reinforcement (MTURR) Coordinating Center Prospective, cohort study NCT01497678 Osteoarthritis; Revision Arthroplasty Venous Thromboembolism Wdrwn Rec 0 Adt Dec-09 Jan-14 Biomet, Inc. Sen http://ClinicalTrials.gov/show/NCT00858598 1660 Adt Aug-10 Jul-12 Boehringer http://ClinicalTrials.gov/show/NCT01139658 Sen Ingelheim Pharmaceuticals Chronic Pain Rec 60 Adt Jun-10 Jun-12 Massachusetts http://ClinicalTrials.gov/show/NCT01137617 Sen General Hospital Orthopedic Disorders Rec 60 Adt Mar-08 Mar-12 Hadassah Sen Medical Organization Degenerative and Rec 12500 Child Sep-10 Mar-12 Arthrex, Inc. Traumatic Pathology Adt of the Knee; Sen Degenerative and Traumatic Pathology of the Shoulder; Degenerative and Traumatic Pathology of the Foot and Ankle Traumatic Injury; Rec 40 Adt Dec-10 Dec-11 University of Muscle Injury; Pittsburgh Tendon Injury; Soft Tissue Injury; Extremity Injury Traumatic Injury; Not yet 40 Adt Feb-12 Dec-11 University of Muscle Injury; Rec Pittsburgh; Tendon Injury; Soft United States Tissue Injury; Naval Medical Extremity Injury Center, Portsmouth 373 http://ClinicalTrials.gov/show/NCT00641823 http://ClinicalTrials.gov/show/NCT01191151 http://ClinicalTrials.gov/show/NCT01292876 http://ClinicalTrials.gov/show/NCT01497678 Inflammatory Cytokine Variations in Traumatic Injury Responses Prospective, case-only study NCT00593892 Inflammatory Active, Cytokine Variations NR Following Traumatic Injury 150 A Comparison of Ultrasound and Nerve Stimulator Techniques for Nerve Localization in Regional Anesthesia Prospective study NCT01221415 Ultrasound Confirmation of Fluoroscopically Guided Piriformis Muscle Injections Prospective, case-only study NCT01390090 The Incidence of TRALI in Patients Undergoing Orthopedic-Oncology Surgery Prospective, case control study NCT00914784 Rapid Identification of Key Pathogens in Wound Infection by Molecular Means Prospective, case-only study NCT00287599 Perfusion Index (PI) and Pleth Variability Index (PVI) in Patients With Interscalene Blocks in Orthopedic Surgery Prospective, case-only study NCT01389011 Transfusion-Associated Microchimerism in Previously Injured Individuals Who Received a Blood Transfusion Retrospective, cohort study NCT00441779 Orthopedic Comp 220 Rec 60 Adt May-07 Dec-11 University of http://ClinicalTrials.gov/show/NCT00593892 Sen Alabama at Birmingham; Orthopaedic Trauma Association Adt Jan-08 Oct-11 Ochsner Health http://ClinicalTrials.gov/show/NCT01221415 Sen System Adt Jan-11 Sep-11 University of Sen Florida http://ClinicalTrials.gov/show/NCT01390090 Dyspnea; Pulmonary Not yet 550 Edema Rec Adt Aug-09 Sep-11 Tel-Aviv Sen Sourasky Medical Center http://ClinicalTrials.gov/show/NCT00914784 Postoperative Wound Infection; Traumatic Wound Infection; Closed Soft Tissue Abscess Perfusion Index and Pleth Variability Index; Interscalene Blocks; Orthopedic Surgery Comp 400 Adt Oct-06 Aug-11 Brentwood Sen Biomedical Research Institute http://ClinicalTrials.gov/show/NCT00287599 Comp 30 Adt Sep-10 Jul-11 Johannes http://ClinicalTrials.gov/show/NCT01389011 Sen Gutenberg University Mainz Chimerism; Blood Transfusion; Wounds and Injuries; Traumatic injuries; Burn injuries; Elective orthopedic operations. Invite 600 Child Aug-08 Jun-11 National Heart, http://ClinicalTrials.gov/show/NCT00441779 Adt Lung, and Blood Sen Institute (NHLBI) Subjects Will Have Failed Conservative Treatment. 374 Collection of Blood, Bone Marrow, Leukapheresis, and Tissue Biopsy Samples From Patients and Their Family Members for Center for Human Immunology, Autoimmunity, and Inflammatory Diseases Laboratory Research Studies NCT01200823 MRI Study of Musculoskeletal Function NCT00051857 Idopathic Inflammatory; Autoimmune Syndromes Rec N/K Child Jun-10 Jun-11 National Heart, http://ClinicalTrials.gov/show/NCT01200823 Adt Lung, and Blood Sen Institute (NHLBI) Healthy Rec Comparison of Three Methods of Hemoglobin Monitoring Prospective, cohort study NCT00792597 Cytogenetic and Molecular Genetic Studies in Bone Sarcomas Prospective, case-only study NCT00579930 Standard Deviation of the Distance Between the Sural Nerve and Achilles Tendon by Ultrasound Cross-sectional study NCT01112605 Evaluation of the Surgical Pleth Index During Spinal and General Anesthesia Prospective, case control study NCT00789438 Blood Loss Comp 500 Child Jan-03 Apr-11 National Adt Institutes of Sen Health Clinical Center (CC) 20 Adt Apr-09 Dec-10 University of Sen California, San Francisco Lung Cancer Susp 0 Healthy Comp 50 Adt Apr-10 May-10 Meir Medical Center http://ClinicalTrials.gov/show/NCT01112605 Stress; Pain Comp 69 Adt Oct-08 May-10 University of Sen SchleswigHolstein http://ClinicalTrials.gov/show/NCT00789438 375 http://ClinicalTrials.gov/show/NCT00051857 http://ClinicalTrials.gov/show/NCT00792597 Child Dec-93 Dec-10 Memorial Sloan- http://ClinicalTrials.gov/show/NCT00579930 Adt Kettering Cancer Sen Center