{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Arthropathy+Shoulder", "query": { "condition": "Arthropathy Shoulder" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 293, "total_pages": 30, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Arthropathy+Shoulder&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-06-10T10:29:05.046Z", "attribution": "Data derived from public ClinicalTrials.gov records. The official record at https://clinicaltrials.gov/ remains the source of truth for current availability, contacts, and full study details.", "notes": [ "This endpoint exposes only public summary fields — no participant contact emails, phone numbers, or scraped investigator contact details.", "For contact information and full protocol detail, follow each trial's `official_url` to the ClinicalTrials.gov record.", "This API is a navigational aid. It does not provide medical advice, eligibility determinations, or compensation guarantees." ], "trials": [ { "nct_id": "NCT07138898", "title": "Immunosuppressant Management in Rheumatology Patients Undergoing Elective Total Shoulder Arthroplasty", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Rheumatic Disease" ], "interventions": [ { "name": "Methotrexate", "type": "DRUG" }, { "name": "Sulfasalazine", "type": "DRUG" }, { "name": "Hydroxychloroquine", "type": "DRUG" }, { "name": "Leflunomide", "type": "DRUG" }, { "name": "Azathioprine", "type": "DRUG" }, { "name": "Mycophenolate", "type": "DRUG" }, { "name": "Cyclosporine", "type": "DRUG" }, { "name": "Tacrolimus", "type": "DRUG" }, { "name": "Etanercept", "type": "DRUG" }, { "name": "Adalimumab", "type": "DRUG" }, { "name": "Golimumab", "type": "DRUG" }, { "name": "Certolizumab", "type": "DRUG" }, { "name": "Infliximab", "type": "DRUG" }, { "name": "Rituximab", "type": "BIOLOGICAL" }, { "name": "Belimumab", "type": "BIOLOGICAL" }, { "name": "Tocilizumab", "type": "BIOLOGICAL" }, { "name": "Anakinra", "type": "BIOLOGICAL" }, { "name": "Canakinumab", "type": "BIOLOGICAL" }, { "name": "Abatacept", "type": "BIOLOGICAL" }, { "name": "Secukinumab", "type": "BIOLOGICAL" }, { "name": "Ixekizumab", "type": "BIOLOGICAL" }, { "name": "Bimekizumab", "type": "BIOLOGICAL" }, { "name": "Ustekinumab", "type": "BIOLOGICAL" }, { "name": "Guselkumab", "type": "BIOLOGICAL" }, { "name": "Risankizumab", "type": "BIOLOGICAL" }, { "name": "Tofacitinib", "type": "DRUG" }, { "name": "Upadacitinib", "type": "DRUG" } ], "intervention_types": [ "DRUG", "BIOLOGICAL" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 80, "start_date": "2025-09", "completion_date": "2027-09", "has_results": false, "last_update_posted_date": "2025-08-24", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07138898" }, { "nct_id": "NCT02995941", "title": "Shoulder Symptom Irritability Scale: A Single-Blinded Observational Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Shoulder Pain", "Pain" ], "interventions": [], "intervention_types": [], "sponsor": "St. Luke's Hospital and Health Network, Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 138, "start_date": "2016-12", "completion_date": "2017-07", "has_results": false, "last_update_posted_date": "2019-09-20", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 17, "location_summary": "Washington, New Jersey • Allentown, Pennsylvania • Bath, Pennsylvania + 11 more", "locations": [ { "city": "Washington", "state": "New Jersey" }, { "city": "Allentown", "state": "Pennsylvania" }, { "city": "Allentown", "state": "Pennsylvania" }, { "city": "Bath", "state": "Pennsylvania" }, { "city": "Bethlehem", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02995941" }, { "nct_id": "NCT03525275", "title": "Effect of Battlefield Acupuncture and Physical Therapy Versus Physical Therapy Alone After Shoulder Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use", "Pain, Postoperative", "SLAP Lesion", "Bankart Lesion", "Subacromial Impingement Syndrome", "Rotator Cuff Tear", "Glenohumeral Dislocation", "Glenohumeral Subluxation", "Hill Sach Lesion", "Bony Bankart Lesion", "Acromioclavicular Separation" ], "interventions": [ { "name": "Battlefield Acupuncture", "type": "DEVICE" }, { "name": "Post-surgical shoulder protocol", "type": "PROCEDURE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "Keller Army Community Hospital", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "17 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "17 Years to 55 Years" }, "enrollment_count": 40, "start_date": "2018-08-15", "completion_date": "2019-04-15", "has_results": false, "last_update_posted_date": "2019-05-20", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "West Point, New York", "locations": [ { "city": "West Point", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03525275" }, { "nct_id": "NCT04968405", "title": "Catalyst CSR Shoulder System for Semi or Total Shoulder Arthroplasty", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Osteoarthritis Shoulder", "Avascular Necrosis of the Head of Humerus", "Rheumatoid Arthritis Shoulder" ], "interventions": [ { "name": "Catalyst CSR Total Shoulder System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Catalyst OrthoScience", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 87, "start_date": "2022-07-22", "completion_date": "2026-02-01", "has_results": false, "last_update_posted_date": "2026-03-31", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 3, "location_summary": "Royal Oak, Michigan • Portland, Oregon • Providence, Rhode Island", "locations": [ { "city": "Royal Oak", "state": "Michigan" }, { "city": "Portland", "state": "Oregon" }, { "city": "Providence", "state": "Rhode Island" } ], "official_url": "https://clinicaltrials.gov/study/NCT04968405" }, { "nct_id": "NCT05703958", "title": "Exactech Proximal Humerus Fracture Plate System Post Market Clinical Follow-up", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Proximal Humeral Fracture", "Fracture Dislocation", "Non-Union Fracture" ], "interventions": [], "intervention_types": [], "sponsor": "Exactech", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 151, "start_date": "2023-04-19", "completion_date": "2034-09-30", "has_results": false, "last_update_posted_date": "2024-10-24", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05703958" }, { "nct_id": "NCT07125833", "title": "Cryoneurolysis of the Suprascapular Nerve for Perioperative Pain Control After Receiving a Reverse Total Shoulder Arthroplasty (RTSA)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Joint Disease of Shoulder" ], "interventions": [ { "name": "Cryoneurolysis", "type": "DEVICE" }, { "name": "No cryoneurolysis", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "North Texas Medical Research Institute, PLLC", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "30 Years to 85 Years" }, "enrollment_count": 20, "start_date": "2025-07-30", "completion_date": "2026-08", "has_results": false, "last_update_posted_date": "2025-08-15", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "Rockwall, Texas", "locations": [ { "city": "Rockwall", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07125833" }, { "nct_id": "NCT01743833", "title": "Effects of Thoracic Orthopedic Manual Therapy and Biopsychosocial Variables on Signs of Shoulder Impingement", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shoulder Impingement" ], "interventions": [ { "name": "Thoracic High Velocity, Low Amplitude Thrust Maneuver (HVLATM)", "type": "OTHER" }, { "name": "Scapular High Velocity, Low Amplitude Thrust Maneuver", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "UConn Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "69 Years", "sex": "ALL", "summary": "18 Years to 69 Years" }, "enrollment_count": 97, "start_date": "2011-06", "completion_date": "2012-12-05", "has_results": false, "last_update_posted_date": "2017-04-26", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "Farmington, Connecticut", "locations": [ { "city": "Farmington", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT01743833" }, { "nct_id": "NCT06536114", "title": "Efficacy of a Criteria Based Clinical Pathway for Rehabilitation of Shoulder Injuries", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Shoulder Pain", "Shoulder Injuries" ], "interventions": [ { "name": "CRISP: Criteria-Based Approach for the Rehabilitation for Non-Operative Shoulder Injuries", "type": "OTHER" }, { "name": "Standard of Care", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "United States Naval Medical Center, San Diego", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 250, "start_date": "2025-03-01", "completion_date": "2027-08-30", "has_results": false, "last_update_posted_date": "2024-08-02", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06536114" }, { "nct_id": "NCT04003311", "title": "MDR - Comprehensive Primary/Micro Stem & Versa-Dial Ti Humeral Head", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Shoulder Pain", "Shoulder Injuries", "Shoulder Fractures", "Shoulder Disease", "Shoulder Arthritis" ], "interventions": [ { "name": "Comprehensive Primary Micro Stem", "type": "DEVICE" }, { "name": "Comprehensive Anatomic Versa-Dial Titanium Humeral Head", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Zimmer Biomet", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 146, "start_date": "2019-12-13", "completion_date": "2028-07-29", "has_results": false, "last_update_posted_date": "2025-10-30", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 4, "location_summary": "Boise, Idaho • Royal Oak, Michigan • Rochester, New York + 1 more", "locations": [ { "city": "Boise", "state": "Idaho" }, { "city": "Royal Oak", "state": "Michigan" }, { "city": "Rochester", "state": "New York" }, { "city": "Burlington", "state": "Vermont" } ], "official_url": "https://clinicaltrials.gov/study/NCT04003311" }, { "nct_id": "NCT00426985", "title": "Efficacy and Safety of Ketoprofen Topical Patch 20% in the Treatment of Pain Associated With Shoulder, Elbow or Knee Tendonitis or Bursitis", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Tendonitis", "Bursitis" ], "interventions": [ { "name": "Ketoprofen Topical Patch 20%", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "APR Applied Pharma Research s.a.", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 381, "start_date": "2007-02-07", "completion_date": "2008-03-10", "has_results": false, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-06-10T10:29:05.046Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00426985" } ] }