{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=FAST&page=47", "query": { "intervention": "FAST", "page": 47 }, "page_size": 10 }, "pagination": { "page": 47, "page_size": 10, "total_count": 3871, "total_pages": 388, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=FAST&page=48&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=FAST&page=46&page_size=10" }, "source": "remote", "last_synced_at": "2026-11-04T05:39:01.353Z", "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": "NCT00534482", "title": "Evaluation of the \"Americans in Motion - Healthy Interventions\" Project", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Activity", "Diet", "Mental Health" ], "interventions": [ { "name": "Enhanced Office", "type": "BEHAVIORAL" }, { "name": "Conventional Office", "type": "BEHAVIORAL" }, { "name": "AIM-HI program with enhanced feedback", "type": "BEHAVIORAL" }, { "name": "AIM-HI program and regular feedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "American Academy of Family Physicians", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 950, "start_date": "2007-07", "completion_date": "2009-10", "has_results": false, "last_update_posted_date": "2011-05-10", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Leawood, Kansas", "locations": [ { "city": "Leawood", "state": "Kansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00534482" }, { "nct_id": "NCT04702529", "title": "Treatment of Fibrotic Scars With Rapid Acoustic Pulse (RAP) Device", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Scars, Hypertrophic" ], "interventions": [ { "name": "Treatment of hypertrophic scars (Soliton's Rapid Acoustic Pulse (RAP) Device)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Soliton", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2022-06-22", "completion_date": "2023-08-31", "has_results": false, "last_update_posted_date": "2024-12-24", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "San Diego, California", "locations": [ { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04702529" }, { "nct_id": "NCT00717145", "title": "Food Effects on the Relative Bioavailability of Different Dosages of Risedronate", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Postmenopausal", "Non-lactating", "Surgically Sterile" ], "interventions": [ { "name": "risedronate", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Warner Chilcott", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": "70 Years", "sex": "FEMALE", "summary": "40 Years to 70 Years · Female only" }, "enrollment_count": 94, "start_date": "2008-07", "completion_date": "2008-09", "has_results": false, "last_update_posted_date": "2011-10-12", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 3, "location_summary": "Gainesville, Florida • Miramar, Florida • Austin, Texas", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Miramar", "state": "Florida" }, { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00717145" }, { "nct_id": "NCT00789672", "title": "Pilot Study to Evaluate Levodopa as Treatment for Residual Amblyopia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Amblyopia" ], "interventions": [ { "name": "levodopa/carbidopa", "type": "DRUG" }, { "name": "patching", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "DEVICE" ], "sponsor": "Jaeb Center for Health Research", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "8 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "8 Years to 17 Years" }, "enrollment_count": 33, "start_date": "2009-01", "completion_date": "2009-12", "has_results": true, "last_update_posted_date": "2016-07-13", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00789672" }, { "nct_id": "NCT01851395", "title": "Rapid Autopsy and Procurement of Cancer Tissue", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Thymus Tumors", "Adoptive Cellular Therapy", "Mesothelioma", "Genitourinary Cancers", "Lung Cancers" ], "interventions": [], "intervention_types": [], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 32, "start_date": "2013-12-30", "completion_date": "2025-10-14", "has_results": false, "last_update_posted_date": "2026-05-05", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01851395" }, { "nct_id": "NCT05489445", "title": "All Inclusive Kodex - EPD Study", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Atrial Fibrillation" ], "interventions": [ { "name": "KODEX - EPD", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Arizona", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15, "start_date": "2021-09-15", "completion_date": "2022-11-02", "has_results": false, "last_update_posted_date": "2023-12-15", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Phoenix, Arizona", "locations": [ { "city": "Phoenix", "state": "Arizona" } ], "official_url": "https://clinicaltrials.gov/study/NCT05489445" }, { "nct_id": "NCT02093637", "title": "Rapid Extremity Pain Relief by Battlefield Acupuncture After Orthopedic Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pain" ], "interventions": [ { "name": "Placebo acupuncture", "type": "OTHER" }, { "name": "Battlefield Acupuncture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Mike O'Callaghan Military Hospital", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 279, "start_date": "2013-08", "completion_date": "2017-02", "has_results": false, "last_update_posted_date": "2017-08-11", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 2, "location_summary": "Travis Air Force Base, California • Nellis Air Force Base, Nevada", "locations": [ { "city": "Travis Air Force Base", "state": "California" }, { "city": "Nellis Air Force Base", "state": "Nevada" } ], "official_url": "https://clinicaltrials.gov/study/NCT02093637" }, { "nct_id": "NCT01489995", "title": "Migalastat Food Effect Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Fabry Disease" ], "interventions": [ { "name": "A (migalastat)", "type": "DRUG" }, { "name": "B (migalastat)", "type": "DRUG" }, { "name": "C (migalastat)", "type": "DRUG" }, { "name": "D (migalastat)", "type": "DRUG" }, { "name": "E (migalastat)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Amicus Therapeutics", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 20, "start_date": "2011-10", "completion_date": "2011-12", "has_results": false, "last_update_posted_date": "2013-12-18", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01489995" }, { "nct_id": "NCT00992095", "title": "Bioequivalency Study of Buprenorphine Hydrochloride 8 mg Tablet Under Fasted Conditions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid-Related Disorders" ], "interventions": [ { "name": "buprenorphine hydrochloride", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Roxane Laboratories", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 48, "start_date": "2006-08", "completion_date": "2006-09", "has_results": false, "last_update_posted_date": "2018-01-23", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00992095" }, { "nct_id": "NCT04388904", "title": "Rapid Reinitiation of a Single Tablet Antiretroviral Therapy Using Symtuza® in HIV-1 Infected Treatment-Experienced Patients Off Therapy. (ReSTART)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "HIV-1-infection" ], "interventions": [ { "name": "Darunavir/Cobicistat/Emtricitabine/Tenofovir Alafenamide (FDC)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "The Crofoot Research Center, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2021-09-01", "completion_date": "2024-04-05", "has_results": false, "last_update_posted_date": "2024-04-26", "last_synced_at": "2026-11-04T05:39:01.353Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04388904" } ] }