{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Trauma+Related+Injuries", "query": { "condition": "Trauma Related Injuries" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 2291, "total_pages": 230, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Trauma+Related+Injuries&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-06-26T06:08:49.117Z", "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": "NCT05240924", "title": "ERP to Improve Functioning in Veterans With OCD", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obsessive Compulsive Disorder (OCD)", "Comorbid Post-Traumatic Stress Disorder and OCD" ], "interventions": [ { "name": "Exposure and Response Prevention", "type": "BEHAVIORAL" }, { "name": "Stress Management Training", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 160, "start_date": "2022-10-03", "completion_date": "2027-05-31", "has_results": false, "last_update_posted_date": "2026-06-08", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 18, "location_summary": "East Orange, New Jersey • Buffalo, New York • New York, New York + 15 more", "locations": [ { "city": "East Orange", "state": "New Jersey" }, { "city": "Buffalo", "state": "New York" }, { "city": "New York", "state": "New York" }, { "city": "Northport", "state": "New York" }, { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT05240924" }, { "nct_id": "NCT03108079", "title": "Bladder Morphology Using 2 Different Catheter Designs", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Urologic Injuries", "Urologic Diseases", "Bladder Infection", "Urinary Tract Infections", "Mucosal Inflammation", "Mucosal Infection", "Bladder Injury", "Catheter-Related Infections", "Catheter Complications", "Catheter; Infection (Indwelling Catheter)", "Pelvic Floor Disorders", "Urinary Incontinence" ], "interventions": [ { "name": "Cystosure Urinary Access System", "type": "DEVICE" }, { "name": "Foley Catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "The Pelvic Floor Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": "70 Years", "sex": "FEMALE", "summary": "21 Years to 70 Years · Female only" }, "enrollment_count": 3, "start_date": "2017-04", "completion_date": "2017-06", "has_results": false, "last_update_posted_date": "2017-04-12", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03108079" }, { "nct_id": "NCT01849029", "title": "Cognitive Processing Intervention for Trauma, HIV/STI Risks, and Substance Use Among Native Women", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post Traumatic Stress Disorders", "Unsafe Sex", "Substance Use Disorders" ], "interventions": [ { "name": "Cognitive Processing Therapy-Cognitive", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 60, "start_date": "2013-10-15", "completion_date": "2017-07-30", "has_results": false, "last_update_posted_date": "2017-08-22", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Toppenish, Washington", "locations": [ { "city": "Toppenish", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT01849029" }, { "nct_id": "NCT05550753", "title": "Better Together Physician Coaching to Mitigate Burnout in Male-Identifying Trainees", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Burnout, Professional", "Self Compassion", "Flourishing", "Imposter Syndrome", "Moral Injury" ], "interventions": [ { "name": "Better Together Physician Coaching Program", "type": "BEHAVIORAL" }, { "name": "No intervention - placebo control", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Colorado, Denver", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "MALE", "summary": "Male only" }, "enrollment_count": 41, "start_date": "2023-01-02", "completion_date": "2023-09-01", "has_results": false, "last_update_posted_date": "2023-09-28", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Aurora, Colorado", "locations": [ { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT05550753" }, { "nct_id": "NCT01848457", "title": "Preventing Nephrotoxicity and Ototoxicity From Osteosarcoma Therapy", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Osteosarcoma", "Nephrotoxicity", "Ototoxicity" ], "interventions": [ { "name": "Pantoprazole", "type": "DRUG" }, { "name": "High-dose methotrexate infusion duration", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Children's Hospital of Philadelphia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": "30 Years", "sex": "ALL", "summary": "Up to 30 Years" }, "enrollment_count": 13, "start_date": "2013-04", "completion_date": "2016-10-01", "has_results": true, "last_update_posted_date": "2020-03-16", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01848457" }, { "nct_id": "NCT03310112", "title": "Mindfulness Training in U.S. Army Cohorts", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Psychological Stress", "Anxiety", "Post Traumatic Stress Disorder", "Depression", "Cognitive Change" ], "interventions": [ { "name": "4-week MBAT", "type": "BEHAVIORAL" }, { "name": "2-week MBAT", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Miami", "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": 120, "start_date": "2017-10-09", "completion_date": "2018-03-27", "has_results": false, "last_update_posted_date": "2018-09-18", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Coral Gables, Florida", "locations": [ { "city": "Coral Gables", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT03310112" }, { "nct_id": "NCT06073886", "title": "Personalized Brain Stimulation to Treat Chronic Concussive Symptoms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Post-Concussion Syndrome", "Concussion, Brain", "Mild Traumatic Brain Injury", "Head Injury", "Headache", "Dizziness", "Cognitive Symptom", "Dysautonomia", "Anxiety", "Irritability; Syndrome", "Depression", "Post-traumatic Stress Disorder" ], "interventions": [ { "name": "Active cTBS", "type": "DEVICE" }, { "name": "Inactive/Sham cTBS", "type": "DEVICE" }, { "name": "Imaginal exposure", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "University of California, Los Angeles", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 75, "start_date": "2024-03-06", "completion_date": "2027-01", "has_results": false, "last_update_posted_date": "2026-02-24", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Westwood, Los Angeles, California", "locations": [ { "city": "Westwood, Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT06073886" }, { "nct_id": "NCT01803802", "title": "Effects of Early Abuse on Adult Intimate Relationships", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Hypoactive Sexual Desire Disorder", "Female Sexual Arousal Disorder", "Female Orgasmic Disorder", "Major Depressive Disorder", "Post-traumatic Stress Disorder" ], "interventions": [ { "name": "Expressive writing", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 148, "start_date": "2005-04", "completion_date": "2014-08", "has_results": false, "last_update_posted_date": "2014-12-02", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01803802" }, { "nct_id": "NCT05223829", "title": "Utility of Brexanolone to Target Stress-induced Alcohol Use Among Men and Women With Posttraumatic Stress Disorder", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "PTSD", "Alcohol Use Disorder" ], "interventions": [ { "name": "Brexanolone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "21 Years to 55 Years" }, "enrollment_count": 25, "start_date": "2023-08-01", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2025-10-14", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT05223829" }, { "nct_id": "NCT01882257", "title": "Home-Based Diagnosis and Management of Sleep-Related Breathing Disorders in Spinal Cord Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Obstructive Sleep Apnea", "Hypercapnia", "Spinal Cord Injury" ], "interventions": [ { "name": "BiPAP", "type": "DEVICE" }, { "name": "BiPAP/AVAPS (Phillips Respironics)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Michigan", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 93, "start_date": "2011-10", "completion_date": "2016-02", "has_results": true, "last_update_posted_date": "2017-01-11", "last_synced_at": "2026-06-26T06:08:49.117Z", "location_count": 1, "location_summary": "Ann Arbor, Michigan", "locations": [ { "city": "Ann Arbor", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01882257" } ] }