{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Closed+Reduction&page=2", "query": { "intervention": "Closed Reduction", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Closed+Reduction&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-11T18:31:27.735Z", "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": "NCT04498143", "title": "Single-Session Intervention Targeting Self-Injurious Behavior in Adolescents", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Nonsuicidal Self Injury", "Self Hatred", "Suicidal Thoughts", "Suicide Attempts" ], "interventions": [ { "name": "Project SAVE (\"Stop Adolescent Violence Everywhere\") SSI", "type": "OTHER" }, { "name": "Active Comparator: Supportive Therapy (\"Share Your Feelings\") SSI", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "13 Years", "maximum_age": "16 Years", "sex": "ALL", "summary": "13 Years to 16 Years" }, "enrollment_count": 565, "start_date": "2020-08-18", "completion_date": "2021-04-14", "has_results": true, "last_update_posted_date": "2024-12-10", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "Denver, Colorado", "locations": [ { "city": "Denver", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04498143" }, { "nct_id": "NCT01865123", "title": "A Randomized Controlled Trial of Meditation Compared to Exposure Therapy and Education Control on PTSD in Veterans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-traumatic Stress Disorder" ], "interventions": [ { "name": "Transcendental Meditation", "type": "BEHAVIORAL" }, { "name": "Prolonged Exposure", "type": "BEHAVIORAL" }, { "name": "Educational control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "United States Department of Defense", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2013-06", "completion_date": "2016-08", "has_results": false, "last_update_posted_date": "2018-11-26", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01865123" }, { "nct_id": "NCT01942356", "title": "Evaluation of Closed-loop TIVA Propofol, Sufentanil and Ketamine Guided by BIS Monitor", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Cholecystitis", "Chronic Cholecystitis" ], "interventions": [ { "name": "TIVA - Hypotension", "type": "PROCEDURE" }, { "name": "TIVA - Hypertension", "type": "PROCEDURE" }, { "name": "TIVA - Bradycardia", "type": "PROCEDURE" }, { "name": "TIVA - Tachycardia", "type": "PROCEDURE" }, { "name": "INH - Hypotension", "type": "PROCEDURE" }, { "name": "INH - Hypertension", "type": "PROCEDURE" }, { "name": "INH - Bradycardia", "type": "PROCEDURE" }, { "name": "INH - Tachycardia", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "The University of Texas Health Science Center at San Antonio", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 4, "start_date": "2013-09", "completion_date": "2014-08", "has_results": false, "last_update_posted_date": "2015-01-27", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "San Antonio, Texas", "locations": [ { "city": "San Antonio", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01942356" }, { "nct_id": "NCT03835065", "title": "Long Arm Vs Short Arm Fiberglass Cast for Treatment of Displaced Distal Radius Fractures", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Distal Forearm Fractures" ], "interventions": [ { "name": "Closed Reduction", "type": "PROCEDURE" }, { "name": "Long Arm Fiberglass Cast", "type": "OTHER" }, { "name": "Short Arm Fiberglass Cast", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Hospital for Special Surgery, New York", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "4 Years", "maximum_age": "12 Years", "sex": "ALL", "summary": "4 Years to 12 Years" }, "enrollment_count": 0, "start_date": "2019-02-12", "completion_date": "2025-02-11", "has_results": false, "last_update_posted_date": "2025-03-24", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03835065" }, { "nct_id": "NCT04219397", "title": "Investigating Interventions to Reduce Residual Opioids in the Home Following Legitimate Opioid Prescribing in Children.", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use, Unspecified" ], "interventions": [ { "name": "Medication take back", "type": "OTHER" }, { "name": "Medication home disposal", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Years", "maximum_age": "18 Years", "sex": "ALL", "summary": "12 Years to 18 Years" }, "enrollment_count": 83, "start_date": "2020-01-23", "completion_date": "2023-01-03", "has_results": false, "last_update_posted_date": "2024-02-15", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 2, "location_summary": "Indianapolis, Indiana • New Orleans, Louisiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" }, { "city": "New Orleans", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT04219397" }, { "nct_id": "NCT02061800", "title": "CD34+ (Malignant) Stem Cell Selection for Patients Receiving Allogenic Stem Cell Transplant", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Chronic Myeloid Leukemia (CML)", "Acute Myelogenous Leukemia (AML)", "Myelodysplastic Syndrome (MDS)", "Juvenile Myelomonocytic Leukemia (JMML)", "Acute Lymphoblastic Leukemia (ALL)", "Lymphoma (Hodgkin's and Non-Hodgkin's)" ], "interventions": [ { "name": "CliniMACS CD34+ Reagent System", "type": "DEVICE" }, { "name": "Thiotepa", "type": "DRUG" }, { "name": "Cyclophosphamide", "type": "DRUG" }, { "name": "Alemtuzumab", "type": "DRUG" }, { "name": "Tacrolimus", "type": "DRUG" }, { "name": "Melphalan", "type": "DRUG" }, { "name": "Busulfan", "type": "DRUG" }, { "name": "Fludarabine", "type": "DRUG" }, { "name": "Methylprednisolone", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Diane George", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "22 Years", "sex": "ALL", "summary": "Up to 22 Years" }, "enrollment_count": 14, "start_date": "2013-06-03", "completion_date": "2026-07", "has_results": false, "last_update_posted_date": "2024-06-04", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02061800" }, { "nct_id": "NCT02032966", "title": "Surgical Versus Nonsurgical Treatment of Fibular Fractures: A Prospective Randomized Study", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Ankle Fracture", "Malleolus Fracture", "Medial Malleolus Fracture", "Bimalleolar Fracture", "Trimalleolar Fracture" ], "interventions": [ { "name": "Nonsurgical", "type": "PROCEDURE" }, { "name": "Surgical", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Tennessee", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 30, "start_date": "2011-04", "completion_date": "2019-12", "has_results": false, "last_update_posted_date": "2018-11-28", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "Chattanooga, Tennessee", "locations": [ { "city": "Chattanooga", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT02032966" }, { "nct_id": "NCT01407263", "title": "Trial of Modifications to Radical Prostatectomy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Prostate Cancer" ], "interventions": [ { "name": "Lymph node template", "type": "PROCEDURE" }, { "name": "Transverse versus vertical closure", "type": "PROCEDURE" }, { "name": "antibiotic prophylaxis", "type": "DRUG" }, { "name": "Hemostatic Agent", "type": "DRUG" } ], "intervention_types": [ "PROCEDURE", "DRUG" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "MALE", "summary": "21 Years and older · Male only" }, "enrollment_count": 3204, "start_date": "2011-07", "completion_date": "2027-07", "has_results": false, "last_update_posted_date": "2026-08-17", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 5, "location_summary": "Basking Ridge, New Jersey • Montvale, New Jersey • Harrison, New York + 2 more", "locations": [ { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Montvale", "state": "New Jersey" }, { "city": "Harrison", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "Uniondale", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01407263" }, { "nct_id": "NCT01681511", "title": "A Trial for the Safety and Effectiveness of a Novel Antimicrobial-Coated Foley Catheter for Reduction of CAUTI.", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urinary Tract Infection" ], "interventions": [ { "name": "ICET™ TIC Foley Catheter", "type": "DEVICE" }, { "name": "BARD® LUBRI-SIL® IC Foley Catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Innovative Chemical and Environmental Technologies, Inc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2012-05", "completion_date": "2013-01", "has_results": true, "last_update_posted_date": "2014-04-28", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "Minneapolis, Minnesota", "locations": [ { "city": "Minneapolis", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01681511" }, { "nct_id": "NCT00330421", "title": "Sorafenib in Treating Patients With Soft Tissue Sarcomas (Extremity Sarcoma Closed to Entry as of 5/30/07)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Metastatic Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "Metastatic Osteosarcoma", "Recurrent Adult Soft Tissue Sarcoma", "Recurrent Ewing Sarcoma/Peripheral Primitive Neuroectodermal Tumor", "Recurrent Osteosarcoma", "Stage I Adult Soft Tissue Sarcoma", "Stage II Adult Soft Tissue Sarcoma", "Stage III Adult Soft Tissue Sarcoma", "Stage IV Adult Soft Tissue Sarcoma" ], "interventions": [ { "name": "sorafenib tosylate", "type": "DRUG" }, { "name": "therapeutic conventional surgery", "type": "PROCEDURE" }, { "name": "laboratory biomarker analysis", "type": "OTHER" }, { "name": "pharmacological study", "type": "OTHER" }, { "name": "computed tomography", "type": "PROCEDURE" }, { "name": "dynamic contrast-enhanced magnetic resonance imaging", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE", "OTHER" ], "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": 15, "start_date": "2006-06", "completion_date": "2008-07", "has_results": true, "last_update_posted_date": "2014-04-30", "last_synced_at": "2026-09-11T18:31:27.735Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT00330421" } ] }