{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Tear&page=2", "query": { "condition": "Muscle Tear", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Muscle+Tear&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-07-23T22:24:22.234Z", "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": "NCT01330641", "title": "Accuracy of Needle Placement Into The Subacromial Space of The Shoulder", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rotator Cuff Tendonitis" ], "interventions": [ { "name": "Injection of Subacromial Bursa", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, Davis", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2008-09", "completion_date": "2011-03", "has_results": false, "last_update_posted_date": "2011-04-07", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Sacramento, California", "locations": [ { "city": "Sacramento", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01330641" }, { "nct_id": "NCT04136743", "title": "Ultrasound-Guided Treatments for Shoulder Pain in Wheelchair Users With Spinal Cord Injury", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Spinal Cord Injuries", "Tendinopathy", "Rotator Cuff Tears", "Shoulder Pain" ], "interventions": [ { "name": "Lipogems", "type": "DEVICE" }, { "name": "Dexamethasone", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Kessler Foundation", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 24, "start_date": "2019-06-14", "completion_date": "2024-04-30", "has_results": false, "last_update_posted_date": "2022-10-14", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "West Orange, New Jersey", "locations": [ { "city": "West Orange", "state": "New Jersey" } ], "official_url": "https://clinicaltrials.gov/study/NCT04136743" }, { "nct_id": "NCT02584452", "title": "Trial Evaluating Postop Pain and Muscle Strength Among Regional Anesthesia Techniques for Ambulatory ACL Reconstruction", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Rupture of Anterior Cruciate Ligament", "Tear of Anterior Cruciate Ligament" ], "interventions": [ { "name": "Mepivacaine", "type": "DRUG" }, { "name": "adductor canal continuous nerve catheter", "type": "PROCEDURE" }, { "name": "Normal Saline as bolus followed by bupivacaine", "type": "DRUG" }, { "name": "adductor canal nerve block", "type": "PROCEDURE" }, { "name": "ropivacaine and dexamethasone", "type": "DRUG" }, { "name": "Propofol", "type": "DRUG" }, { "name": "Fentanyl", "type": "DRUG" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Vanderbilt University Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "ALL", "summary": "14 Years and older" }, "enrollment_count": 59, "start_date": "2015-11-03", "completion_date": "2018-04-10", "has_results": true, "last_update_posted_date": "2019-12-11", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02584452" }, { "nct_id": "NCT03307499", "title": "NeoPatch Used as Adjunct in Foot and Ankle Tendon Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tendinopathy", "Tendon Tear", "Tendon Injuries", "Foot Ankle Injuries" ], "interventions": [ { "name": "NeoPatch", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "CryoLife, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 7, "start_date": "2017-09-21", "completion_date": "2019-05-15", "has_results": false, "last_update_posted_date": "2019-05-24", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Sycamore, Illinois", "locations": [ { "city": "Sycamore", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03307499" }, { "nct_id": "NCT07721220", "title": "Acute Effects of Neurodynamics on Strength and Endurance in Athletes", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Sciatic Leg Pain", "Hamstring Muscle Tightness", "Hamstring Muscle Strain", "Hamstring Muscle Strength", "Hamstring Injuries", "Hamstring Injury Prevention", "Hamstring Rupture", "Sciatic Nerve Injury", "Sciatic Radiculopathy", "Lumbar Disc Herniation With Radiculopathy", "Lumbar Disc Herniation" ], "interventions": [ { "name": "Sciatic Slider", "type": "OTHER" }, { "name": "Sciatic Tensioner", "type": "OTHER" }, { "name": "Mechanically loaded neurodynamic sciatic floss", "type": "OTHER" }, { "name": "Elastic Resistance Band", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "High Point University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 45, "start_date": "2026-06-15", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2026-07-22", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "High Point, North Carolina", "locations": [ { "city": "High Point", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT07721220" }, { "nct_id": "NCT01550094", "title": "A Comparison of Two Injection Locations in Obese Patients Having Lower Leg/Foot Surgery", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Strain of Muscle and/or Tendon of Lower Leg", "Fracture of Lower Leg", "Crushing Injury of Lower Leg", "Fracture Malunion - 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" ], "interventions": [], "intervention_types": [], "sponsor": "Jose Soberon, MD", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 60, "start_date": "2012-03", "completion_date": "2015-10", "has_results": false, "last_update_posted_date": "2015-10-14", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "New Orleans, Louisiana", "locations": [ { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT01550094" }, { "nct_id": "NCT06571695", "title": "Restoring the Anatomic Tension Relationship of the Long Head of the Biceps During Tenodesis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Biceps Tendon Disorder", "Tendinosis", "Rotator Cuff Injuries" ], "interventions": [ { "name": "Anatomic Long Head of Biceps Tensioning Technique", "type": "PROCEDURE" }, { "name": "Traditional Long Head of Biceps Tensioning Technique", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Loyola University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 204, "start_date": "2020-10-27", "completion_date": "2024-02-20", "has_results": true, "last_update_posted_date": "2024-11-20", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Maywood, Illinois", "locations": [ { "city": "Maywood", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06571695" }, { "nct_id": "NCT07498166", "title": "Project Tendura: The Impact of Blood Flow Restriction Resistance Training (BFR-RT) in Patients With Achilles Tendon Rupture (ATR) Repair", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Achilles Tendon Rupture", "Blood Flow Restriction Therapy", "Achilles Tendon Repairs/Reconstructions", "Dynamic Blood Flow Restriction" ], "interventions": [ { "name": "Blood Flow Restriction Resistance Training (BFR-RT)", "type": "DEVICE" }, { "name": "Sham Blood Flow Restriction", "type": "DEVICE" }, { "name": "Standard Physical Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 75, "start_date": "2026-02-01", "completion_date": "2027-02-01", "has_results": false, "last_update_posted_date": "2026-04-01", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07498166" }, { "nct_id": "NCT04057833", "title": "E-CEL UVEC Cells as an Adjunct Cell Therapy for the Arthroscopic Rotator Cuff Repair in Adults", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Rotator Cuff Tears", "Muscle Atrophy or Weakness", "Tendon Rupture - Shoulder", "Safety Issues" ], "interventions": [ { "name": "E-CEL UVEC", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Hospital for Special Surgery, New York", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "45 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "45 Years to 70 Years" }, "enrollment_count": 20, "start_date": "2019-11-20", "completion_date": "2026-10", "has_results": false, "last_update_posted_date": "2025-11-26", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04057833" }, { "nct_id": "NCT01833936", "title": "E-Stim and Achilles Tendon Repair Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Achilles Tendon Rupture" ], "interventions": [ { "name": "Compex® muscle stimulator", "type": "DEVICE" }, { "name": "(inactive) muscle stimulator", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Orthopedic Foot and Ankle Center, Ohio", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2013-01", "completion_date": "2016-09-22", "has_results": true, "last_update_posted_date": "2018-01-10", "last_synced_at": "2026-07-23T22:24:22.234Z", "location_count": 1, "location_summary": "Westerville, Ohio", "locations": [ { "city": "Westerville", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01833936" } ] }