{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Trauma+Management+Therapy&page=2", "query": { "intervention": "Trauma Management Therapy", "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=Trauma+Management+Therapy&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-19T20:20:35.273Z", "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": "NCT03211884", "title": "Effects of PSTon Mental Health Outcomes in Caregivers of Post-9/11 Combat Veterans With a Traumatic Brain Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Military Family", "Brain Injuries, Traumatic" ], "interventions": [ { "name": "Problem-Solving Thearpy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Duquesne University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 149, "start_date": "2017-07-13", "completion_date": "2020-07-15", "has_results": false, "last_update_posted_date": "2021-03-24", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03211884" }, { "nct_id": "NCT04667468", "title": "Cold Stored Platelet in Hemorrhagic Shock", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Trauma", "Hemorrhage" ], "interventions": [ { "name": "Cold Stored Platelets (CSP)", "type": "BIOLOGICAL" }, { "name": "Standard Care", "type": "BIOLOGICAL" } ], "intervention_types": [ "BIOLOGICAL" ], "sponsor": "Jason Sperry", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "15 Years to 90 Years" }, "enrollment_count": 200, "start_date": "2022-06-21", "completion_date": "2023-11-20", "has_results": true, "last_update_posted_date": "2024-12-18", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 5, "location_summary": "Los Angeles, California • San Francisco, California • Jackson, Mississippi + 1 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Jackson", "state": "Mississippi" }, { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04667468" }, { "nct_id": "NCT04019314", "title": "Assessment of ProEnkephalin to Detect Acute Kidney Injury (AKI)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Heart Failure", "Volume Overload", "Decompensated Heart Failure", "Systolic Heart Failure" ], "interventions": [ { "name": "Blood Collection", "type": "PROCEDURE" }, { "name": "Blood Volume Analysis", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 20, "start_date": "2019-06-11", "completion_date": "2021-10-06", "has_results": false, "last_update_posted_date": "2022-08-23", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT04019314" }, { "nct_id": "NCT04989504", "title": "Testing the Application of Mepitel Film During Radiation Therapy to Reduce Radiation Related Redness and Peeling in Breast Cancer Patients Following Mastectomy", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Breast Carcinoma", "Mastectomy Patient" ], "interventions": [ { "name": "Best Practice", "type": "OTHER" }, { "name": "Wound Dressing Material", "type": "DEVICE" }, { "name": "Quality-of-Life Assessment", "type": "OTHER" }, { "name": "Questionnaire Administration", "type": "OTHER" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Alliance for Clinical Trials in Oncology", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 216, "start_date": "2022-07-26", "completion_date": "2029-02-15", "has_results": true, "last_update_posted_date": "2025-04-29", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 49, "location_summary": "Marysville, California • Truckee, California • Frankford, Delaware + 39 more", "locations": [ { "city": "Marysville", "state": "California" }, { "city": "Truckee", "state": "California" }, { "city": "Frankford", "state": "Delaware" }, { "city": "Newark", "state": "Delaware" }, { "city": "Newark", "state": "Delaware" } ], "official_url": "https://clinicaltrials.gov/study/NCT04989504" }, { "nct_id": "NCT01789216", "title": "Improving Pain Management and Long Term Outcomes Following High Energy Orthopedic Trauma (Pain Study)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Orthopaedic Fractures" ], "interventions": [ { "name": "NSAID", "type": "DRUG" }, { "name": "Gabapentinoids", "type": "DRUG" }, { "name": "placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Major Extremity Trauma Research Consortium", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 450, "start_date": "2013-07", "completion_date": "2018-12-31", "has_results": false, "last_update_posted_date": "2021-02-03", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 17, "location_summary": "Miami, Florida • West Palm Beach, Florida • Indianapolis, Indiana + 13 more", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "West Palm Beach", "state": "Florida" }, { "city": "Indianapolis", "state": "Indiana" }, { "city": "Iowa City", "state": "Iowa" }, { "city": "Shreveport", "state": "Louisiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT01789216" }, { "nct_id": "NCT00591448", "title": "Study in the Use of Virtual Reality as an Adjunct to Pain Control in Burn Patients", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Burn" ], "interventions": [ { "name": "Virtual Reality (VR)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Wisconsin, Madison", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "6 Years", "maximum_age": null, "sex": "ALL", "summary": "6 Years and older" }, "enrollment_count": 10, "start_date": "2007-10", "completion_date": "2008-08", "has_results": false, "last_update_posted_date": "2012-10-17", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Madison, Wisconsin", "locations": [ { "city": "Madison", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT00591448" }, { "nct_id": "NCT00675714", "title": "Assessment of the Treatment of Severely Burned With Anabolic Agents on Clinical Outcomes, Recovery and Rehabilitation", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Burns" ], "interventions": [ { "name": "Stable Isotope Infusion Study", "type": "PROCEDURE" }, { "name": "Collection of blood and tissues", "type": "PROCEDURE" }, { "name": "Radiology testing: Dual-energy X-ray absorptiometry (DEXA), ultrasound, MRI", "type": "PROCEDURE" }, { "name": "Humatrope", "type": "DRUG" }, { "name": "Ketoconazole", "type": "DRUG" }, { "name": "Oxandrolone", "type": "DRUG" }, { "name": "Propranolol", "type": "DRUG" }, { "name": "Oxandrolone and propranolol combined", "type": "DRUG" }, { "name": "Humatrope and propranolol combined", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Exercise--Hospital supervised intensive exercise program", "type": "BEHAVIORAL" }, { "name": "Home exercise program", "type": "BEHAVIORAL" } ], "intervention_types": [ "PROCEDURE", "DRUG", "BEHAVIORAL" ], "sponsor": "The University of Texas Medical Branch, Galveston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "80 Years", "sex": "ALL", "summary": "Up to 80 Years" }, "enrollment_count": 1126, "start_date": "2004-01", "completion_date": "2019-07-15", "has_results": false, "last_update_posted_date": "2019-11-29", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Galveston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00675714" }, { "nct_id": "NCT01681004", "title": "Investigation of Sacroiliac Fusion Treatment (INSITE)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Degenerative Sacroiliitis", "Sacroiliac Joint Disruption" ], "interventions": [ { "name": "iFuse Implant System", "type": "DEVICE" }, { "name": "Non-surgical management", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "SI-BONE, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "21 Years to 70 Years" }, "enrollment_count": 159, "start_date": "2012-09", "completion_date": "2017-06", "has_results": true, "last_update_posted_date": "2017-08-25", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 19, "location_summary": "La Jolla, California • Newport Beach, California • Denver, Colorado + 16 more", "locations": [ { "city": "La Jolla", "state": "California" }, { "city": "Newport Beach", "state": "California" }, { "city": "Denver", "state": "Colorado" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "Daytona Beach", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01681004" }, { "nct_id": "NCT07332143", "title": "Psilocybin-Assisted Therapy", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "PTSD" ], "interventions": [ { "name": "psilocybin", "type": "DRUG" }, { "name": "Supportive Therapy", "type": "BEHAVIORAL" }, { "name": "Prolonged Exposure Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": "2026-06", "completion_date": "2027-03", "has_results": false, "last_update_posted_date": "2026-05-26", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Atlanta, Georgia", "locations": [ { "city": "Atlanta", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07332143" }, { "nct_id": "NCT00937235", "title": "Treatment of Smoking Among Individuals With PTSD", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Cigarette Smoking", "Nicotine Dependence", "Post-traumatic Stress Disorder", "Tobacco Use Disorder" ], "interventions": [ { "name": "Varenicline", "type": "DRUG" }, { "name": "Medication Management Counseling", "type": "BEHAVIORAL" }, { "name": "Prolonged Exposure", "type": "BEHAVIORAL" } ], "intervention_types": [ "DRUG", "BEHAVIORAL" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 142, "start_date": "2009-01", "completion_date": "2015-12", "has_results": true, "last_update_posted_date": "2017-11-14", "last_synced_at": "2026-09-19T20:20:35.273Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00937235" } ] }