| Rank |
Status |
Study |
| 1 |
Unknown †
|
Validation of Ultrasound as a Diagnostic Tool for Assessment of Hemophilic Arthropathy of Knees and Ankles
| Conditions: |
Hemophilia; Hemophilic Arthropathy |
| Intervention: |
|
| Outcome Measures: |
Ultrasound findings according to the International Prophylaxis Study Group (IPSG) scale; MRI findings according to the International Prophylaxis Study Group (IPSG) scale; X-ray findings according to the Pettersson radiographic system; Physical Assessment according to the HJHS and FISH scores |
|
| 2 |
Recruiting
|
Safety Study of Univers® Revers Shoulder Prosthesis
| Condition: |
Rotator Cuff Tear Arthropathy |
| Intervention: |
Device: Universe Reverse Prosthesis |
| Outcome Measures: |
SADE within 2 years po; Risk of adverse events intra-operatively, and post-operatively up to 2 years follow-up; Prosthesis survival at 2, 5 and 10 years; Constant (Murley) score (CS); The Shoulder Pain and Disability Index (SPADI); Short version of the Disability of the Arm, Shoulder and Hand questionnaire (QuickDASH); EuroQoL EQ-5D-5L; Patient satisfaction; Radiographic Parameters; Patient active and passive range of motion (ROM) and shoulder strength |
|
| 3 |
Recruiting
|
Osteopathic Manipulation for Female Interstitial Cystitis Patients With Sacroiliac Joint Dysfunction
| Conditions: |
Interstitial Cystitis; Sacroiliac Joint Somatic Dysfunction |
| Intervention: |
Procedure: Osteopathic Manipulation Therapy |
| Outcome Measure: |
Improvement in Scores of Validated questionnaires pertaining to Interstitial Cystitis problems and symptoms |
|
| 4 |
Recruiting
|
Anakinra to Treat Patients With Neonatal Onset Multisystem Inflammatory Disease
| Conditions: |
Nervous System Malformations; Arthropathy, Neurogenic; Urticaria; Papilledema |
| Intervention: |
|
| Outcome Measure: |
Comparison of group mean of total disease diary score before compared to after treatment (3-4 mo); mean change in the area under the curve in SAA in patients before and 3-4 mo after tx as well as before and after drug withdrawal. |
|
| 5 |
Unknown †
|
Synvisc Injections for Lumbar Facet Joint Pain
| Condition: |
Joint Pain |
| Intervention: |
Procedure: Synvisc viscosupplementation |
| Outcome Measures: |
Visual Analogue Scale (VAS) for baseline pain (best, worst, average) and pain while walking; Oswestry Disability Questionnaire; Short Form 36-Item (SF-36); Standing/walking tolerance (defined as time patient can sit for before pain level reaches baseline or distance walked before pain reaches baseline); Analgesic usage; Lumbar range of motion; Patient satisfaction |
|
| 6 |
Recruiting
|
Transplantation of Bone Marrow Stem Cells Stimulated by Proteins Scaffold to Heal Defects Articular Cartilage of the Knee
| Conditions: |
Osteoarthritis; Knee Osteoarthritis; Osteochondritis Dissecans; Osteonecrosis |
| Intervention: |
Procedure: Transplantation of Bone Marrow Stem Cells Activated in Knee Arthrosis |
| Outcome Measures: |
IKS, International Knee Score; KOOS, Knee Injury and Osteoarthritis Outcome Score |
|
| 7 |
Recruiting
|
Studies of the Natural History and Pathogenesis and Outcome of Neonatal Onset Multisystem Inflammatory Disease (NOMID/CAPS, DIRA, CRMO, Still s Disease, Behcet s Disease, and Other Undifferentiated Autoinflammatory Diseases)
| Conditions: |
Urticaria; Arthropathy; Lymphadenopathy; Nervous System Anomalies |
| Intervention: |
|
| Outcome Measure: |
|
|
| 8 |
Recruiting
|
Radiofrequency Nerve Ablation Versus Sham to Treat Chronic Low Back Pain Caused by Sacroiliac Joint Dysfunction
| Condition: |
Sacroiliac Joint Dysfunction |
| Intervention: |
|
| Outcome Measures: |
Reduction in pain; Economic outcomes |
|
| 9 |
Unknown †
|
Gait Evaluation in Haemophiliac Patients
| Conditions: |
Hemophilia A; Hemophilia B |
| Intervention: |
|
| Outcome Measure: |
evaluate specific changes in gait in patients suffering from haemophilic Arthropathy |
|
| 10 |
Recruiting
|
A Prospective, Multicenter, Single Arm Feasibility Study of the Safety and Performance of GRADION™ Hip Total Cartilage Replacement (TCR)™ in the Treatment of Degenerative Joint Disease of the Hip
| Condition: |
Degenerative Joint Disease of the Hip |
| Intervention: |
Device: GRADION™ Hip Total Cartilage Replacement (TCR)™ |
| Outcome Measure: |
Adverse events |
|
| 11 |
Unknown †
|
Impact of Conservative Treatment by Custom-Made Orthoses in Patients With Haemophilic Ankle Arthropathy
| Conditions: |
Haemophilia A; Haemophilia B |
| Intervention: |
Device: custom-molded insoles and custom-molded shoes |
| Outcome Measure: |
Gait analysis, foot pressure measurement, specific joint score |
|
| 12 |
Recruiting
|
The Norwegian Antirheumatic Drug Register
| Condition: |
Inflammatory Joint Diseases |
| Intervention: |
|
| Outcome Measures: |
Disease Activity Score-28 (DAS28); American College of Rheumatology (ACR) responses (ACR20, ACR50, ACR70); Simplified Disease Activity Index (SDAI); American College of Rheumatology (ACR)/European League Against Rheumatism (EULAR) remission; Ankylosing Spondylitis Disease Activity Score (ASDAS); Assessments of Spondyloarthritis International Society (ASAS) responses (ASAS20, ASAS40); Bath Ankylosing Spondylitis Disease Activity Index (BASDAI); Modified Health Assessment Questionnaire (MHAQ); Rheumatoid Arthritis Impact of Disease (RAID); Work Productivity and Activity Impairment (WPAI) Questionnaire; EuroQol 5-dimensions (EQ-5D) questionnaire; 28-Swollen joint count; 28-Tender joint count; Erythrocyte Sedimentation Rate (ESR); C-Reactive Protein (CRP); Sharp/van der Heijde score; Number of participants with adverse events; Clinical Disease Activity Index (CDAI) |
|
| 13 |
Recruiting
|
Study of Adalimumab to Lower Cardiovascular Risk in RA Patients With Well Controlled Joint Disease
| Conditions: |
Rheumatoid Arthritis; Cardiovascular Disease |
| Interventions: |
Drug: Adalimumab; Drug: Placebo |
| Outcome Measures: |
Change in Endothelial Function; Change in vascular inflammation |
|
| 14 |
Recruiting
|
Treatment of Sacroiliac Dysfunction With SI-LOK® Sacroiliac Joint Fixation SI-SI-LOK
| Condition: |
Joint Dysfunction |
| Intervention: |
Device: SI-LOK |
| Outcome Measures: |
Radiographic Evaluation; Hospitalization Data |
|
| 15 |
Recruiting
|
Nocipoint Therapy Versus Standard Physical Therapy Using Electrical Stimulation in Treating Pain From TMJ Disorder
| Condition: |
Temporomandibular Joint Disorders |
| Interventions: |
Procedure: Nocipoint Therapy; Procedure: Physical Therapy |
| Outcome Measures: |
Visual Analog Scale (VAS) for pain; Maximal mouth opening range (MMO); Quality of Life (QoL) |
|
| 16 |
Recruiting
|
A Double Blind Study Comparing Hyaluronic Acid, Corticosteroid and Placebo During Arthrocentesis for TMJ
| Conditions: |
Temporomandibular Joint Dysfunction; Pain; Arthrocentesis |
| Interventions: |
Drug: Hyaluronic acid; Drug: Corticosteroid; Drug: Lactated Ringers |
| Outcome Measures: |
Pain; Function |
|
| 17 |
Unknown †
|
2-Year Post-Approval Study to Investigate the Scandinavian Total Ankle Replacement System (STAR) Ankle Under Actual Conditions of Use
| Conditions: |
Primary Arthrosis; Post Traumatic Arthritis; Rheumatoid Arthritis; Osteoarthritis |
| Intervention: |
Device: Scandinavian Total Ankle Replacement System (STAR Ankle) |
| Outcome Measures: |
The principal endpoint consists of evaluating the safety and effectiveness of the STAR Ankle using the same composite definition of patient success used in the IDE study.; American Orthopaedic Foot and Ankle Society Score questionnaire will be used to evaluate and monitor the progress of patients following foot and ankle surgery. |
|
| 18 |
Not yet recruiting
|
Study of Association Between Digital Osteoarthritis and Lower Limb Osteoarthritis
| Condition: |
Digital Arthrosis |
| Intervention: |
Radiation: Hand X-rays |
| Outcome Measures: |
Kellgren and Lawrence score; Harris score |
|
| 19 |
Recruiting
|
COMPREHENSIVE® REVERSE SHOULDER Mini BasePlate
| Conditions: |
Rotator Cuff Tear Arthropathy; Osteoporosis; Osteomalacia; Joint; Destruction, Sacroiliac |
| Intervention: |
Device: COMPREHENSIVE |
| Outcome Measures: |
Survivorship; Adverse Events (including dislocation); Constant-Murley Shoulder Score; Radiographic Evaluation (Plain X-ray and CT); Scapular Notching; Radiographic Evaluation |
|
| 20 |
Unknown †
|
Effects of Masseter Manual Therapy on Temporomandibular Dysfunction
| Conditions: |
Temporomandibular Joint; Temporomandibular Joint Dysfunction Syndrome; Temporomandibular Joint Disorder |
| Intervention: |
Procedure: Active release techniques |
| Outcome Measures: |
Range of Motion; VAS pain scale |
|
