{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Early+Life+Trauma", "query": { "condition": "Early Life Trauma" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 12, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Early+Life+Trauma&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-07-23T18:12:51.298Z", "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": "NCT07278505", "title": "Study of Cannabidiol and Neuroimaging on Stress", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Early Life Adversity", "Trauma", "Stress" ], "interventions": [ { "name": "Cannabidiol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Icahn School of Medicine at Mount Sinai", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "18 Years to 25 Years" }, "enrollment_count": 160, "start_date": "2025-10-28", "completion_date": "2030-02-28", "has_results": false, "last_update_posted_date": "2025-12-12", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07278505" }, { "nct_id": "NCT05729828", "title": "Psychometric Properties of the SMART Feeding Tool", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Feeding; Difficult, Newborn", "Premature Infant Disease", "Dysphagia of Newborn", "Nurse's Role", "Feeding Disorder of Infancy or Early Childhood", "Trauma and Stressor Related Disorders", "Deglutition Disorders in Infants", "Malnutrition, Infant" ], "interventions": [], "intervention_types": [], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "33 Weeks", "maximum_age": "50 Weeks", "sex": "ALL", "summary": "33 Weeks to 50 Weeks" }, "enrollment_count": 76, "start_date": "2021-05-05", "completion_date": "2022-02-10", "has_results": false, "last_update_posted_date": "2024-12-11", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 4, "location_summary": "Chicago, Illinois • Downers Grove, Illinois • Oak Lawn, Illinois + 1 more", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Downers Grove", "state": "Illinois" }, { "city": "Oak Lawn", "state": "Illinois" }, { "city": "Park Ridge", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05729828" }, { "nct_id": "NCT00851214", "title": "Use of Non Invasive Hemodynamic Cardiovascular Monitoring to Evaluate Emergency Department Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "COPD", "Congestive Heart Failure", "Trauma", "Sepsis", "Stroke" ], "interventions": [ { "name": "NexfinHD Monitor", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2009-03", "completion_date": "2009-06", "has_results": false, "last_update_posted_date": "2010-02-18", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT00851214" }, { "nct_id": "NCT03083366", "title": "Sacral Nerve Stimulation in Improving Bladder Function After Acute Traumatic Spinal Cord Injury", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injury, Acute", "Neurogenic Bladder", "Incontinence", "Urinary Tract Infections" ], "interventions": [ { "name": "PrimeAdvanced Surescan 97702 Neurostimulator - Medtronic (Minneapolis, MN)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5, "start_date": "2019-08-07", "completion_date": "2023-04-20", "has_results": true, "last_update_posted_date": "2025-06-10", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 2, "location_summary": "Downey, California • Salt Lake City, Utah", "locations": [ { "city": "Downey", "state": "California" }, { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT03083366" }, { "nct_id": "NCT03479541", "title": "Can Early Initiation of Rehabilitation With Wearable Sensor Technology Improve Outcomes in mTBI?", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Mild Traumatic Brain Injury", "Balance; Distorted", "Gait, Unsteady", "Quality of Life", "Veterans" ], "interventions": [ { "name": "Timing of Rehabilitation", "type": "BEHAVIORAL" }, { "name": "Biofeedback", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Oregon Health and Science University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 203, "start_date": "2018-07-15", "completion_date": "2023-09-30", "has_results": true, "last_update_posted_date": "2025-06-24", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Portland, Oregon", "locations": [ { "city": "Portland", "state": "Oregon" } ], "official_url": "https://clinicaltrials.gov/study/NCT03479541" }, { "nct_id": "NCT07369115", "title": "Neurocircuitry Mechanisms and Efficacy of Lumateperone as Adjunctive Therapy for Major Depressive Disorder and History of Early Life Abuse", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Major Depressive Diorder", "Early Life Trauma" ], "interventions": [ { "name": "Lumateperone 42 mg", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "21 Years to 70 Years" }, "enrollment_count": 50, "start_date": "2026-02", "completion_date": "2030-01", "has_results": false, "last_update_posted_date": "2026-01-27", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07369115" }, { "nct_id": "NCT01701258", "title": "An Investigation of Early Life Stress and Depression", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Major Depressive Disorder (MDD)", "History of Childhood Sexual Abuse (CSA)" ], "interventions": [ { "name": "Amisulpride", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mclean Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "20 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "20 Years to 45 Years · Female only" }, "enrollment_count": 153, "start_date": "2013-08", "completion_date": "2017-05", "has_results": true, "last_update_posted_date": "2025-05-07", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 2, "location_summary": "Belmont, Massachusetts • Boston, Massachusetts", "locations": [ { "city": "Belmont", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01701258" }, { "nct_id": "NCT06938542", "title": "Palliative Care Needs of Children With Rare Diseases and Their Families", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Trisomy 13 Syndrome", "Arthrogryposis Congenita Multiplex With Intestinal Atresia", "Asparagine Synthetase Deficiency", "CHARGE Syndrome", "Early Infantile Epileptic Encephalopathy", "FOXG1 Syndrome", "KBG Syndrome", "Noonan Syndrome", "Severe Hemophilia A", "Short Bowel Syndrome", "Beta-Propeller Protein-Associated Neurodegeneration", "Brain Injury of Prematurity With Periventricular Leukomalacia", "Chromosome 17p13.3 Microdeletion Syndrome", "Chromosome 1q43-1q44 Deletion", "Cockayne Syndrome", "Congenital Diaphragmatic Hernia", "End-Stage Renal Disease With Cloacal Anomaly", "Mitochondrial Depletion Disorder", "Severe Factor VII Deficiency" ], "interventions": [ { "name": "Family Centered pediatric palliative care for family caregivers of children with rare diseases.", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Children's National Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "12 Months", "maximum_age": "99 Years", "sex": "ALL", "summary": "12 Months to 99 Years" }, "enrollment_count": 480, "start_date": "2025-10-02", "completion_date": "2029-08-02", "has_results": false, "last_update_posted_date": "2026-01-28", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT06938542" }, { "nct_id": "NCT04060121", "title": "Efficacy of Psychological Therapies in Patients With Functional Bowel Disorders", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "IBS - Irritable Bowel Syndrome", "Constipation" ], "interventions": [], "intervention_types": [], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 126, "start_date": "2018-06-01", "completion_date": "2022-11-29", "has_results": false, "last_update_posted_date": "2024-04-29", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT04060121" }, { "nct_id": "NCT04713722", "title": "Early Life Stress and Depression: Molecular and Functional Imaging", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Depression", "Trauma, Psychological" ], "interventions": [], "intervention_types": [], "sponsor": "Mclean Hospital", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "20 Years", "maximum_age": "32 Years", "sex": "FEMALE", "summary": "20 Years to 32 Years · Female only" }, "enrollment_count": 160, "start_date": "2021-02-01", "completion_date": "2026-06-30", "has_results": false, "last_update_posted_date": "2025-12-12", "last_synced_at": "2026-07-23T18:12:51.298Z", "location_count": 1, "location_summary": "Belmont, Massachusetts", "locations": [ { "city": "Belmont", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04713722" } ] }