{
  "api_version": "1",
  "request": {
    "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Medial+Epicondylitis",
    "query": {
      "condition": "Medial Epicondylitis"
    },
    "page_size": 10
  },
  "pagination": {
    "page": 1,
    "page_size": 10,
    "total_count": 4,
    "total_pages": 1,
    "next_page_url": null,
    "previous_page_url": null
  },
  "source": "remote",
  "last_synced_at": "2026-05-22T07:37:03.319Z",
  "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": "NCT01525043",
      "title": "Study to Evaluate the Efficacy of the Synera Patch Compared to Naproxen Sodium for Epicondylitis of the Elbow",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE4"
      ],
      "conditions": [
        "Epicondylitis of the Elbow"
      ],
      "interventions": [
        {
          "name": "Naproxen",
          "type": "DRUG"
        },
        {
          "name": "Synera patch twice daily",
          "type": "DRUG"
        },
        {
          "name": "Synera patch for 12hrs/day",
          "type": "DRUG"
        },
        {
          "name": "Synera",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "International Clinical Research Institute",
      "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": 78,
      "start_date": "2012-02",
      "completion_date": "2013-09",
      "has_results": false,
      "last_update_posted_date": "2014-03-05",
      "last_synced_at": "2026-05-22T07:37:03.319Z",
      "location_count": 1,
      "location_summary": "Overland Park, Kansas",
      "locations": [
        {
          "city": "Overland Park",
          "state": "Kansas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT01525043"
    },
    {
      "nct_id": "NCT03782298",
      "title": "Safety and Performance of PEEK Anchors in Extremities",
      "overall_status": "COMPLETED",
      "study_type": "OBSERVATIONAL",
      "phases": [],
      "conditions": [
        "Medial or Lateral Instability Repairs/Reconstructions",
        "Hallux Valgus Repairs",
        "Achilles Tendon Repairs/Reconstructions",
        "Midfoot Reconstructions",
        "Metatarsal Ligament/Tendon Repairs/Reconstructions",
        "Bunionectomy",
        "Scapholunate Ligament Reconstructions",
        "Ulnar",
        "Lateral Epicondylitis Repair",
        "Bicep Tendon Reattachments"
      ],
      "interventions": [
        {
          "name": "Spyromite, Dynomite, Raptomite, Footprint Ultra PK SL",
          "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": 140,
      "start_date": "2019-03-12",
      "completion_date": "2019-10-10",
      "has_results": true,
      "last_update_posted_date": "2024-10-01",
      "last_synced_at": "2026-05-22T07:37:03.319Z",
      "location_count": 3,
      "location_summary": "Charlotte, North Carolina • Chardon, Ohio • Grapevine, Texas",
      "locations": [
        {
          "city": "Charlotte",
          "state": "North Carolina"
        },
        {
          "city": "Chardon",
          "state": "Ohio"
        },
        {
          "city": "Grapevine",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT03782298"
    },
    {
      "nct_id": "NCT04686799",
      "title": "Doxycycline for Elbow Tendinopathy",
      "overall_status": "COMPLETED",
      "study_type": "INTERVENTIONAL",
      "phases": [
        "PHASE1"
      ],
      "conditions": [
        "Lateral Epicondylitis",
        "Lateral Epicondylitis, Left Elbow",
        "Lateral Epicondylitis, Right Elbow",
        "Lateral Epicondylitis, Unspecified Elbow",
        "Lateral Epicondylitis (Tennis Elbow) Bilateral",
        "Medial Epicondylitis",
        "Medial Epicondylitis, Right Elbow",
        "Medial Epicondylitis, Left Elbow"
      ],
      "interventions": [
        {
          "name": "Doxycycline Hyclate 20 MG",
          "type": "DRUG"
        }
      ],
      "intervention_types": [
        "DRUG"
      ],
      "sponsor": "Hospital for Special Surgery, New York",
      "sponsor_class": "OTHER",
      "healthy_volunteers": false,
      "eligibility": {
        "minimum_age": "18 Years",
        "maximum_age": null,
        "sex": "ALL",
        "summary": "18 Years and older"
      },
      "enrollment_count": 21,
      "start_date": "2020-12-03",
      "completion_date": "2025-10-09",
      "has_results": false,
      "last_update_posted_date": "2026-04-28",
      "last_synced_at": "2026-05-22T07:37:03.319Z",
      "location_count": 1,
      "location_summary": "New York, New York",
      "locations": [
        {
          "city": "New York",
          "state": "New York"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT04686799"
    },
    {
      "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": "2026-05-22T07:37:03.319Z",
      "location_count": 1,
      "location_summary": "Austin, Texas",
      "locations": [
        {
          "city": "Austin",
          "state": "Texas"
        }
      ],
      "official_url": "https://clinicaltrials.gov/study/NCT00640939"
    }
  ]
}