{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=FT", "query": { "intervention": "FT" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 59, "total_pages": 6, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=FT&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-10T12:11:54.501Z", "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": "NCT03490825", "title": "Aging Program Project Grant 6", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Improving Cardiometabolic Outcomes in Older Adults" ], "interventions": [ { "name": "Melatonin 1 mg", "type": "DIETARY_SUPPLEMENT" }, { "name": "Placebos", "type": "DIETARY_SUPPLEMENT" }, { "name": "Meal timing", "type": "OTHER" }, { "name": "Non-Meal timing", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "OTHER" ], "sponsor": "Northwestern University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "55 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "55 Years to 75 Years" }, "enrollment_count": 32, "start_date": "2018-03-01", "completion_date": "2024-05-31", "has_results": false, "last_update_posted_date": "2025-05-23", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT03490825" }, { "nct_id": "NCT03670524", "title": "Health, Environment and Action in Louisville (HEAL) Green Heart Louisville Project", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cardiovascular Diseases", "Metabolic Health" ], "interventions": [ { "name": "Greenness as a therapeutic intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Louisville", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "30 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "30 Years to 70 Years" }, "enrollment_count": 835, "start_date": "2018-05-03", "completion_date": "2028-10-30", "has_results": false, "last_update_posted_date": "2026-02-10", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Louisville, Kentucky", "locations": [ { "city": "Louisville", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT03670524" }, { "nct_id": "NCT05564390", "title": "MYELOMATCH: A Screening Study to Assign People With Myeloid Cancer to a Treatment Study or Standard of Care Treatment Within myeloMATCH (MyeloMATCH Screening Trial)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Myeloid Leukemia", "Acute Myeloid Leukemia Arising From Previous Myelodysplastic/Myeloproliferative Neoplasm", "Acute Myeloid Leukemia Post Cytotoxic Therapy", "Acute Myeloid Leukemia, Myelodysplasia-Related", "Myelodysplastic Syndrome" ], "interventions": [ { "name": "Allogeneic Hematopoietic Stem Cell Transplantation", "type": "PROCEDURE" }, { "name": "Azacitidine", "type": "DRUG" }, { "name": "Best Practice", "type": "OTHER" }, { "name": "Biopsy Procedure", "type": "PROCEDURE" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Bone Marrow Aspiration", "type": "PROCEDURE" }, { "name": "Bone Marrow Biopsy", "type": "PROCEDURE" }, { "name": "Busulfan", "type": "DRUG" }, { "name": "Chest Radiography", "type": "PROCEDURE" }, { "name": "Computed Tomography", "type": "PROCEDURE" }, { "name": "Cytarabine", "type": "DRUG" }, { "name": "Daunorubicin Hydrochloride", "type": "DRUG" }, { "name": "Decitabine and Cedazuridine", "type": "DRUG" }, { "name": "Echocardiography Test", "type": "PROCEDURE" }, { "name": "Emavusertib", "type": "BIOLOGICAL" }, { "name": "Enasidenib", "type": "DRUG" }, { "name": "Epoetin Alfa", "type": "BIOLOGICAL" }, { "name": "Fludarabine", "type": "DRUG" }, { "name": "Gemtuzumab Ozogamicin", "type": "DRUG" }, { "name": "Gilteritinib", "type": "DRUG" }, { "name": "Liposome-encapsulated Daunorubicin-Cytarabine", "type": "DRUG" }, { "name": "Luspatercept", "type": "BIOLOGICAL" }, { "name": "Melphalan", "type": "DRUG" }, { "name": "Multigated Acquisition Scan", "type": "PROCEDURE" }, { "name": "Mutation Carrier Screening", "type": "PROCEDURE" }, { "name": "Olutasidenib", "type": "DRUG" }, { "name": "Placebo Administration", "type": "DRUG" }, { "name": "Positron Emission Tomography", "type": "PROCEDURE" }, { "name": "Total-Body Irradiation", "type": "RADIATION" }, { "name": "Venetoclax", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG", "OTHER", "BIOLOGICAL", "RADIATION" ], "sponsor": "National Cancer Institute (NCI)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2000, "start_date": "2024-06-18", "completion_date": "2029-05-15", "has_results": false, "last_update_posted_date": "2026-09-10", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 336, "location_summary": "Birmingham, Alabama • Phoenix, Arizona • Tucson, Arizona + 259 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Phoenix", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Tucson", "state": "Arizona" }, { "city": "Little Rock", "state": "Arkansas" } ], "official_url": "https://clinicaltrials.gov/study/NCT05564390" }, { "nct_id": "NCT01825564", "title": "Comparison of RightSpot pH Indicator & RightLevel pH Detector With X-Ray Verification for FT or G-Tube Placement", "overall_status": "TERMINATED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Gastrostomy" ], "interventions": [], "intervention_types": [], "sponsor": "St. Louis University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 11, "start_date": "2013-03-14", "completion_date": "2016-05-25", "has_results": false, "last_update_posted_date": "2017-01-24", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "St Louis, Missouri", "locations": [ { "city": "St Louis", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT01825564" }, { "nct_id": "NCT07115914", "title": "PSMA PET for Surveillance After Focal Therapy", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer (Adenocarcinoma)", "Prostate Cancer (Diagnosis)", "Prostate Cancer Metastatic Disease" ], "interventions": [ { "name": "PSMA PET/CT scan", "type": "RADIATION" } ], "intervention_types": [ "RADIATION" ], "sponsor": "University of Chicago", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 62, "start_date": "2025-11-19", "completion_date": "2028-08-01", "has_results": false, "last_update_posted_date": "2026-02-17", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT07115914" }, { "nct_id": "NCT07039396", "title": "Prospective Case Series Evaluating the Efficacy and Safety of NeoThelium FT for Diabetic Foot Ulcers", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Diabetic Foot Ulcer" ], "interventions": [ { "name": "NeoThelium FT (HCT/P 361)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "NuScience Medical Biologics, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2025-08-26", "completion_date": "2026-06-01", "has_results": false, "last_update_posted_date": "2026-03-12", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 3, "location_summary": "Alexandria, Louisiana • Leesville, Louisiana • Many, Louisiana", "locations": [ { "city": "Alexandria", "state": "Louisiana" }, { "city": "Leesville", "state": "Louisiana" }, { "city": "Many", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT07039396" }, { "nct_id": "NCT04073823", "title": "A Study Evaluating FT-SW in Unilateral Breast Cancer-Related Lymphedema Patients", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Breast Cancer Related Lymphedema" ], "interventions": [ { "name": "Flexitouch Plus", "type": "DEVICE" }, { "name": "Flexitouch Plus FT with software modification", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Tactile Medical", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 2, "start_date": "2020-01-23", "completion_date": "2020-02-08", "has_results": true, "last_update_posted_date": "2023-01-18", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04073823" }, { "nct_id": "NCT02118688", "title": "Efficacy and Safety of Risperidone and Trazodone Monotherapy and Combination Therapy in Critically Ill Patients With Delirium", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Delirium", "Agitation" ], "interventions": [ { "name": "Risperidone", "type": "DRUG" }, { "name": "Trazodone", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Rochester General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2011-03", "completion_date": "2016-03", "has_results": false, "last_update_posted_date": "2019-09-10", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Rochester, New York", "locations": [ { "city": "Rochester", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02118688" }, { "nct_id": "NCT04053504", "title": "Feasibility Study of Family Teamwork Peer-Delivery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 1 Diabetes" ], "interventions": [ { "name": "Family Teamwork-Peer Delivery", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "10 Years", "sex": "ALL", "summary": "4 Years to 10 Years" }, "enrollment_count": 60, "start_date": "2019-05-04", "completion_date": "2022-05-01", "has_results": false, "last_update_posted_date": "2022-07-25", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04053504" }, { "nct_id": "NCT04715139", "title": "Evaluate the Continued Safety and Performance of the Foot and Ankle Products", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Hyperpronated Foot", "Reconstruction Surgeries of the Foot", "Fixation of Fractures and Fusion (Bunionectomy Osteotomies) of the Foot/Ankle", "Fixation of Small Bone Fragments of the Foot/Ankle", "Lisfranc Arthrodesis", "Mono or Bi-cortical Osteotomies in the Forefoot", "First Metatarsophalangeal Arthrodesis", "Akin Osteotomy", "Midfoot and Hindfoot Arthrodeses or Osteotomies", "Fixation of Osteotomies for Hallux Valgus Treatment (Scarf and Chevron)", "Arthrodesis of the Metatarsocuneiform Joint to Reposition and Stabilize Metatarsus Primus Varus", "Osteotomy Fixation of Hallux Valgus Repair (Such as Scarf and Chevron Etc.)", "Medial Ankle Stabilization", "Tibiotalocalcaneal Arthrodesis" ], "interventions": [ { "name": "Products listed in Group/Cohort Description", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Arthrex, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 700, "start_date": "2020-12-01", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2026-02-11", "last_synced_at": "2026-09-10T12:11:54.501Z", "location_count": 5, "location_summary": "Sacramento, California • Chicago, Illinois • Nashville, Tennessee + 2 more", "locations": [ { "city": "Sacramento", "state": "California" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Nashville", "state": "Tennessee" }, { "city": "San Antonio", "state": "Texas" }, { "city": "Virginia Beach", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT04715139" } ] }