{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Stress+Disorders%2C+Traumatic%2C+Acute", "query": { "condition": "Stress Disorders, Traumatic, Acute" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 57, "total_pages": 6, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Stress+Disorders%2C+Traumatic%2C+Acute&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-05-22T05:12:42.207Z", "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": "NCT01013870", "title": "Mission Connect Mild Traumatic Brain Injury (TBI) Integrated Clinical Protocol", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Traumatic Brain Injury", "Post-traumatic Stress Disorder" ], "interventions": [ { "name": "Atorvastatin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "50 Years", "sex": "ALL", "summary": "18 Years to 50 Years" }, "enrollment_count": 52, "start_date": "2010-02", "completion_date": "2015-06", "has_results": true, "last_update_posted_date": "2017-01-09", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 2, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" }, { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01013870" }, { "nct_id": "NCT03496545", "title": "Efficacy of Bromocriptine For Fever Reduction in Acute Neurologic Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Subarachnoid Hemorrhage", "Subdural Hematoma", "Traumatic Brain Injury", "Ischemic Stroke", "Fever", "Intracerebral Hemorrhage" ], "interventions": [ { "name": "Bromocriptine 5 MG", "type": "DRUG" }, { "name": "Acetaminophen 650 MG", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 47, "start_date": "2018-11-30", "completion_date": "2019-11-02", "has_results": true, "last_update_posted_date": "2021-06-24", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 2, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03496545" }, { "nct_id": "NCT06349616", "title": "Cooling Strategies for Older Adults in the Heat", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Aging" ], "interventions": [ { "name": "Intermittent cold-water hand and forearm immersion", "type": "OTHER" }, { "name": "No intermittent cold-water hand and forearm immersion", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Penn State University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "65 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "65 Years to 100 Years" }, "enrollment_count": 12, "start_date": "2024-05-01", "completion_date": "2025-07-21", "has_results": false, "last_update_posted_date": "2025-07-24", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "University Park, Pennsylvania", "locations": [ { "city": "University Park", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06349616" }, { "nct_id": "NCT00974467", "title": "Evaluating a Website for Parents of Injured Children", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Acute Post-Traumatic Stress Disorder" ], "interventions": [ { "name": "After The Injury website", "type": "BEHAVIORAL" }, { "name": "Control", "type": "OTHER" } ], "intervention_types": [ "BEHAVIORAL", "OTHER" ], "sponsor": "Children's Hospital of Philadelphia", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "6 Years", "maximum_age": null, "sex": "ALL", "summary": "6 Years and older" }, "enrollment_count": 100, "start_date": "2009-05", "completion_date": "2011-12", "has_results": false, "last_update_posted_date": "2015-03-12", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00974467" }, { "nct_id": "NCT06928116", "title": "Heat thErapy And mobiLity in COVID-19 Survivors", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Long COVID" ], "interventions": [ { "name": "Heat therapy", "type": "BEHAVIORAL" }, { "name": "Sham Control", "type": "BEHAVIORAL" }, { "name": "Walking", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Nebraska", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "50 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "50 Years to 90 Years" }, "enrollment_count": 99, "start_date": "2025-09-17", "completion_date": "2029-08", "has_results": false, "last_update_posted_date": "2025-10-23", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Omaha, Nebraska", "locations": [ { "city": "Omaha", "state": "Nebraska" } ], "official_url": "https://clinicaltrials.gov/study/NCT06928116" }, { "nct_id": "NCT06982183", "title": "The Effects of Propranolol and Hydrocortisone on Military-Relevant Performance Outcomes", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Fear of Spiders", "Acute Stress Reaction" ], "interventions": [ { "name": "Propranolol", "type": "DRUG" }, { "name": "Hydrocortisone", "type": "DRUG" }, { "name": "Placebo (oral)", "type": "DRUG" }, { "name": "Placebo (IM)", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Walter Reed Army Institute of Research (WRAIR)", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "40 Years", "sex": "ALL", "summary": "18 Years to 40 Years" }, "enrollment_count": 88, "start_date": "2025-05-27", "completion_date": "2026-09", "has_results": false, "last_update_posted_date": "2026-05-13", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Silver Spring, Maryland", "locations": [ { "city": "Silver Spring", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06982183" }, { "nct_id": "NCT01407146", "title": "Acute Coronary Syndrome and Care-Seeking Delay: A Web Based Behavioral Study", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Acute Myocardial Infarction", "Heart Attack", "Acute Coronary Syndrome", "Unstable Angina" ], "interventions": [], "intervention_types": [], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 2381, "start_date": "2011-07", "completion_date": "2013-04", "has_results": false, "last_update_posted_date": "2020-04-03", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT01407146" }, { "nct_id": "NCT00050804", "title": "Evaluation of Stress Disorders", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Acute Traumatic Stress Disorders", "Post-Traumatic Stress Disorders" ], "interventions": [ { "name": "sertraline", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "National Institute of Mental Health (NIMH)", "sponsor_class": "NIH", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 80, "start_date": "2002-12", "completion_date": "2004-02", "has_results": false, "last_update_posted_date": "2008-03-04", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00050804" }, { "nct_id": "NCT04806620", "title": "Unhide® Project: A Digital Health Platform to Collect Lifestyle Data for Brain Inflammation Research", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post-Acute COVID-19 Syndrome", "ME/CFS", "Rheumatic Arthritis", "Juvenile Rheumatoid Arthritis (JRA)", "Psoriatic Arthritis (PsA)", "Ankylosing Spondylitis (AS)", "Autoimmune Encephalitis", "Celiac Disease", "Celiac Disease in Children", "Chronic Lyme Disease", "Post-treatment Lyme Disease Syndrome", "Crohn's Disease", "Dysautonomia", "Anorexia Nervosa", "Bulimia Nervosa", "ARFID", "Avoidant / Restrictive Food Intake Disorder", "Ehlers Danlos Syndrome", "Endometriosis", "Fibromyalgia (FM)", "Long COVID", "Lupus", "Migraines", "Mast Cell Activation Syndrome", "Multiple Sclerosis", "Myalgic Encephalomyelitis (ME)", "Myasthenia Gravis, Generalized", "Myasthenia Gravis in Children", "Narcolepsy", "Obsessive Compulsive Disorder (OCD)", "PANDAS", "Pediatric Acute-onset Neuropsychiatric Syndrome (PANS)", "POTS - Postural Orthostatic Tachycardia Syndrome", "General Anxiety Disorder, Social Anxiety Disorder", "PTSD - Post Traumatic Stress Disorder", "Psoriasis", "Traumatic Brain Injury", "Tourette's Syndrome", "Inflammatory Bowel Disease (IBD)", "Autoimmune Diseases", "Neurological Diseases or Conditions", "Psychiatric Disorder", "Sjogren's Syndrome", "Ulcerative Colitis and Crohn's Disease" ], "interventions": [], "intervention_types": [], "sponsor": "Brain Inflammation Collaborative", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 10000, "start_date": "2023-07-05", "completion_date": "2030-12-31", "has_results": false, "last_update_posted_date": "2026-01-22", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Delafield, Wisconsin", "locations": [ { "city": "Delafield", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04806620" }, { "nct_id": "NCT00186472", "title": "Intervention to Decrease Anxiety in Parents of Infants in the Neonatal Intensive Care Unit (NICU)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety", "Acute Stress Disorder", "Posttraumatic Stress Disorder", "Depression" ], "interventions": [ { "name": "Brief Cognitive Behavioral Treatment", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": null, "start_date": null, "completion_date": null, "has_results": false, "last_update_posted_date": "2011-06-02", "last_synced_at": "2026-05-22T05:12:42.207Z", "location_count": 1, "location_summary": "Stanford, California", "locations": [ { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00186472" } ] }