{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Rotator+Cuff+Injury",
    "query": {
      "condition": "Rotator Cuff Injury"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 175,
    "total_pages": 18,
    "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Rotator+Cuff+Injury&page=2&page_size=10",
    "previous_page_url": null
  },
  "source": "remote",
  "last_synced_at": "2026-07-21T23:11:51.569Z",
  "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": "NCT03806842",
      "title": "Easytech Reversed Shoulder System Clinical Study",
      "overall_status": "UNKNOWN",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Osteo Arthritis Shoulders",
        "Avascular Necrosis of the Head of Humerus",
        "Rotator Cuff Tear"
      ],
      "interventions": [
        {
          "name": "Easytech group",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "FX Shoulder Solutions",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "21 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "21 Years and older"
      },
      "enrollment_count": 90,
      "start_date": "2018-11-28",
      "completion_date": "2024-12-28",
      "has_results": false,
      "last_update_posted_date": "2023-09-28",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 6,
      "location_summary": "Sun City West, Arizona • Menlo Park, California • Philadelphia, Pennsylvania + 3 more",
      "locations": [
        {
          "city": "Sun City West",
          "state": "Arizona"
        },
        {
          "city": "Menlo Park",
          "state": "California"
        },
        {
          "city": "Philadelphia",
          "state": "Pennsylvania"
        },
        {
          "city": "Wakefield",
          "state": "Rhode Island"
        },
        {
          "city": "Bedford",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03806842"
    },
    {
      "nct_id": "NCT03577379",
      "title": "Vascular Changes of Rotator Cuff Repair Augmented With a Whole Blood Fibrin Clot",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Rotator Cuff Tear"
      ],
      "interventions": [
        {
          "name": "Whole Blood Fibrin Clot",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Santa Barbara Cottage Hospital",
      "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": 53,
      "start_date": "2019-03-01",
      "completion_date": "2022-04-25",
      "has_results": false,
      "last_update_posted_date": "2022-05-05",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "Santa Barbara, California",
      "locations": [
        {
          "city": "Santa Barbara",
          "state": "California"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03577379"
    },
    {
      "nct_id": "NCT07455474",
      "title": "Clinical Research Study of the Benefits of BREG Polar Care Wave to Reduce Opioid Use by Patients Having Undergone Arthroscopic Rotator Cuff Repair Shoulder Surgery",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Rotator Cuff Tear"
      ],
      "interventions": [
        {
          "name": "Breg Polar Care Wave Cold Compression Device",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "University of Nevada, Reno",
      "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": 50,
      "start_date": "2023-10-01",
      "completion_date": "2026-03-03",
      "has_results": false,
      "last_update_posted_date": "2026-03-06",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 2,
      "location_summary": "Mammoth Lakes, California • Taos, New Mexico",
      "locations": [
        {
          "city": "Mammoth Lakes",
          "state": "California"
        },
        {
          "city": "Taos",
          "state": "New Mexico"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07455474"
    },
    {
      "nct_id": "NCT00640939",
      "title": "Diclofenac Patch for Treatment of Mild to Moderate Tendonitis or Bursitis",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2",
        "PHASE3"
      ],
      "conditions": [
        "Rotator Cuff Tendonitis",
        "Bicipital Tendonitis",
        "Subdeltoid Bursitis of the Shoulder",
        "Subacromial Bursitis of the Shoulder",
        "Medial Epicondylitis of the Elbow",
        "Lateral Epicondylitis of the Elbow",
        "DeQuervain's Tenosynovitis of the Wrist"
      ],
      "interventions": [
        {
          "name": "diclofenac sodium",
          "type": "DRUG"
        },
        {
          "name": "Matching Placebo",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Cerimon Pharmaceuticals",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "18 Years to 75 Years"
      },
      "enrollment_count": 308,
      "start_date": "2007-12",
      "completion_date": "2008-06",
      "has_results": false,
      "last_update_posted_date": "2008-08-06",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "Austin, Texas",
      "locations": [
        {
          "city": "Austin",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00640939"
    },
    {
      "nct_id": "NCT03332238",
      "title": "Stromal Vascular Fraction Cell Therapy to Improve the Repair of Rotator Cuff Tears",
      "overall_status": "ACTIVE_NOT_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE2"
      ],
      "conditions": [
        "Rotator Cuff Tear",
        "Muscle Atrophy",
        "Tendon Tear"
      ],
      "interventions": [
        {
          "name": "Autologous Stomal Vascular Fraction Material",
          "type": "DEVICE"
        },
        {
          "name": "Ringer's solution",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Hospital for Special Surgery, New York",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "45 Years",
        "maximum_age": "65 Years",
        "sex": "ALL",
        "summary": "45 Years to 65 Years"
      },
      "enrollment_count": 56,
      "start_date": "2019-07-01",
      "completion_date": "2026-07-23",
      "has_results": false,
      "last_update_posted_date": "2026-04-28",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03332238"
    },
    {
      "nct_id": "NCT07158892",
      "title": "Understanding Patient Preferences When Deciding on a Voluntary Musculoskeletal Test",
      "overall_status": "NOT_YET_RECRUITING",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Non-traumatic Musculoskeletal Conditions",
        "Carpal Tunnel Syndrome (CTS)",
        "Lateral Epicondylitis",
        "Osteoarthritis",
        "Trigger Digit",
        "Dupuytren Contracture",
        "Rotator Cuff Tendinopathy",
        "De Quervain Disease"
      ],
      "interventions": [
        {
          "name": "Diagnostic Advance Care Planning Discussion",
          "type": "BEHAVIORAL"
        },
        {
          "name": "Informational Statement Only",
          "type": "BEHAVIORAL"
        }
      ],
      "intervention_types": [
        "BEHAVIORAL"
      ],
      "sponsor": "University of Texas at Austin",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 220,
      "start_date": "2025-09-10",
      "completion_date": "2026-03-01",
      "has_results": false,
      "last_update_posted_date": "2025-09-08",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "Austin, Texas",
      "locations": [
        {
          "city": "Austin",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT07158892"
    },
    {
      "nct_id": "NCT03245320",
      "title": "Clinical Evaluation of the TITAN™ Total Shoulder System",
      "overall_status": "TERMINATED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Arthritis",
        "Arthritis, Degenerative",
        "Rheumatoid Arthritis",
        "Post-traumatic Arthrosis of Other Joints, Shoulder Region",
        "Rotator Cuff Syndrome of Shoulder and Allied Disorders",
        "Fracture",
        "Avascular Necrosis",
        "Joint Instability",
        "Joint Trauma",
        "Dislocation, Shoulder",
        "Pain, Shoulder"
      ],
      "interventions": [
        {
          "name": "Integra TITAN™ Total Shoulder Generation 1.0",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Smith & Nephew, Inc.",
      "sponsor_class": "INDUSTRY",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 50,
      "start_date": "2017-03-20",
      "completion_date": "2022-06-23",
      "has_results": false,
      "last_update_posted_date": "2023-12-21",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 2,
      "location_summary": "Indianapolis, Indiana • Philadelphia, Pennsylvania",
      "locations": [
        {
          "city": "Indianapolis",
          "state": "Indiana"
        },
        {
          "city": "Philadelphia",
          "state": "Pennsylvania"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03245320"
    },
    {
      "nct_id": "NCT01355757",
      "title": "Post-Operative Quality of Life Evaluation for Different Anesthesia Techniques for Arthroscopic Shoulder Surgery",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "EARLY_PHASE1"
      ],
      "conditions": [
        "Rotator Cuff Injury"
      ],
      "interventions": [
        {
          "name": "Baxter INFUSOR System",
          "type": "DEVICE"
        },
        {
          "name": "Single Injection of Local Anesthetic",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DEVICE",
        "DRUG"
      ],
      "sponsor": "St. Luke's-Roosevelt Hospital Center",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "18 Years to 75 Years"
      },
      "enrollment_count": 70,
      "start_date": "2011-06",
      "completion_date": "2013-01",
      "has_results": false,
      "last_update_posted_date": "2014-05-19",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01355757"
    },
    {
      "nct_id": "NCT01383239",
      "title": "Impact of Postoperative Management on Outcomes and Healing of Rotator Cuff Repairs",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Rotator Cuff Tear"
      ],
      "interventions": [
        {
          "name": "Immediate Postoperative Therapy",
          "type": "OTHER"
        },
        {
          "name": "Delayed Physical Therapy",
          "type": "OTHER"
        }
      ],
      "intervention_types": [
        "OTHER"
      ],
      "sponsor": "Vanderbilt University",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "100 Years",
        "sex": "ALL",
        "summary": "18 Years to 100 Years"
      },
      "enrollment_count": 27,
      "start_date": "2011-09",
      "completion_date": "2016-07",
      "has_results": false,
      "last_update_posted_date": "2016-11-04",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 9,
      "location_summary": "San Francisco, California • Boulder, Colorado • Iowa City, Iowa + 6 more",
      "locations": [
        {
          "city": "San Francisco",
          "state": "California"
        },
        {
          "city": "Boulder",
          "state": "Colorado"
        },
        {
          "city": "Iowa City",
          "state": "Iowa"
        },
        {
          "city": "Ann Arbor",
          "state": "Michigan"
        },
        {
          "city": "St Louis",
          "state": "Missouri"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01383239"
    },
    {
      "nct_id": "NCT06669741",
      "title": "Clinical Outcomes Related to Arthroscopic Rotator Cuff Repair Recovery Using Incrediwear",
      "overall_status": "ENROLLING_BY_INVITATION",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "NA"
      ],
      "conditions": [
        "Rotator Cuff Tears",
        "Rotator Cuff Injuries",
        "Rotator Cuff Arthropathy of Left Shoulder (Disorder)",
        "Rotator Cuff Arthropathy of Right Shoulder (Disorder)",
        "Rotator Cuff Arthropathy of Bilateral Shoulders"
      ],
      "interventions": [
        {
          "name": "Placebo",
          "type": "DEVICE"
        },
        {
          "name": "Shoulder Sleeve",
          "type": "DEVICE"
        }
      ],
      "intervention_types": [
        "DEVICE"
      ],
      "sponsor": "Texas Bone and Joint",
      "sponsor_class": "OTHER",
      "healthy_volunteers": true,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": "75 Years",
        "sex": "ALL",
        "summary": "18 Years to 75 Years"
      },
      "enrollment_count": 140,
      "start_date": "2024-11-11",
      "completion_date": "2026-12-02",
      "has_results": false,
      "last_update_posted_date": "2025-05-08",
      "last_synced_at": "2026-07-21T23:11:51.569Z",
      "location_count": 1,
      "location_summary": "Denton, Texas",
      "locations": [
        {
          "city": "Denton",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT06669741"
    }
  ]
}