{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reference&page=5", "query": { "intervention": "Reference", "page": 5 }, "page_size": 10 }, "pagination": { "page": 5, "page_size": 10, "total_count": 1503, "total_pages": 151, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reference&page=6&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Reference&page=4&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-21T06:08:49.977Z", "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": "NCT06728969", "title": "A Comparative Study to Evaluate a Novel Algorithm As a Diagnostic Aid for ADHD in Youth Ages 6-17.", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "ADHD" ], "interventions": [ { "name": "MT1 Auditory startle response patterns analysis algorithm", "type": "DEVICE" }, { "name": "T.O.V.A. Continuous Performance Test", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "MindTension", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "6 Years to 17 Years" }, "enrollment_count": 120, "start_date": "2024-06-02", "completion_date": "2026-06", "has_results": false, "last_update_posted_date": "2024-12-11", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06728969" }, { "nct_id": "NCT07222995", "title": "Hybrid Effectiveness-Implementation Trial to Integrate Precision Skin Cancer Risk Feedback in FQHCs", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Skin Cancer" ], "interventions": [ { "name": "Precision Prevention Booklet", "type": "BEHAVIORAL" }, { "name": "Standard Prevention Booklet", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "H. Lee Moffitt Cancer Center and Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2900, "start_date": "2025-10-10", "completion_date": "2030-10-10", "has_results": false, "last_update_posted_date": "2026-02-05", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 2, "location_summary": "Tampa, Florida • New York, New York", "locations": [ { "city": "Tampa", "state": "Florida" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07222995" }, { "nct_id": "NCT05508750", "title": "Growth and Safety Clinical Trial on a New Infant Formula", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Weight Gain" ], "interventions": [ { "name": "New Infant Formula", "type": "OTHER" }, { "name": "Commercial Infant Formula", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Jovie USA, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "0 Days", "maximum_age": "14 Days", "sex": "ALL", "summary": "0 Days to 14 Days" }, "enrollment_count": 420, "start_date": "2022-09-21", "completion_date": "2024-01-02", "has_results": false, "last_update_posted_date": "2024-01-17", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05508750" }, { "nct_id": "NCT04743921", "title": "Effects of Reparel™ Knee Sleeve on Knee Osteoarthritis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Knee Osteoarthritis" ], "interventions": [ { "name": "Reparel Knee Sleeve", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Alabama at Birmingham", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 14, "start_date": "2021-02-01", "completion_date": "2021-11-06", "has_results": true, "last_update_posted_date": "2024-05-16", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "Birmingham, Alabama", "locations": [ { "city": "Birmingham", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT04743921" }, { "nct_id": "NCT03545789", "title": "Phase 1 Test-retest Evaluation of [18F]MNI-958 PET", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy Volunteers", "Alzheimer Disease", "Progressive Supranuclear Palsy" ], "interventions": [ { "name": "[18F]MNI-958", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Invicro", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 16, "start_date": "2018-03-12", "completion_date": "2020-02-06", "has_results": false, "last_update_posted_date": "2020-02-17", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT03545789" }, { "nct_id": "NCT00902187", "title": "A Bioequivalence Study Of 4 Mg Fesoterodine Extended-Release Tablets (Toviaz™) In Healthy Subjects", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Treatment of Overactive Bladder" ], "interventions": [ { "name": "Fesoterodine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Pfizer", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 36, "start_date": "2009-05", "completion_date": "2009-06", "has_results": false, "last_update_posted_date": "2018-10-16", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT00902187" }, { "nct_id": "NCT01072643", "title": "Sedation With Dexmedetomidine During Cardiac Catheterization", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Pulmonary Hypertension" ], "interventions": [ { "name": "Dexmedetomidine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Aruna Nathan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "21 Years", "sex": "ALL", "summary": "8 Years to 21 Years" }, "enrollment_count": 4, "start_date": "2010-03", "completion_date": "2013-04", "has_results": true, "last_update_posted_date": "2019-04-16", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01072643" }, { "nct_id": "NCT01775904", "title": "A Study of Two Dosage Forms of LY2886721 in Healthy Participants", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Healthy Volunteers" ], "interventions": [ { "name": "LY2886721 in a Capsule", "type": "DRUG" }, { "name": "LY2886721 in an orally disintegrating tablet (ODT)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Eli Lilly and Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 26, "start_date": "2013-02", "completion_date": "2013-05", "has_results": true, "last_update_posted_date": "2019-07-19", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT01775904" }, { "nct_id": "NCT04593043", "title": "Replication of the RELY Anticoagulant Trial in Healthcare Claims Data", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Atrial Fibrillation" ], "interventions": [ { "name": "Warfarin", "type": "DRUG" }, { "name": "Dabigatran", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Brigham and Women's Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 78140, "start_date": "2020-01-01", "completion_date": "2021-02-18", "has_results": false, "last_update_posted_date": "2023-07-27", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04593043" }, { "nct_id": "NCT05662982", "title": "Sub-Ischial Socket for Transfemoral Amputation and Lower Mobility", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Transfemoral Amputation" ], "interventions": [ { "name": "Northwestern University Flexible Subischial Suction Socket (NU-FlexSIS)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 84, "start_date": "2023-03-01", "completion_date": "2025-11-30", "has_results": false, "last_update_posted_date": "2025-12-15", "last_synced_at": "2026-10-21T06:08:49.977Z", "location_count": 3, "location_summary": "Minneapolis, Minnesota • Houston, Texas • Seattle, Washington", "locations": [ { "city": "Minneapolis", "state": "Minnesota" }, { "city": "Houston", "state": "Texas" }, { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT05662982" } ] }