{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Brain+Injury%2C+Vascular&page=2", "query": { "condition": "Brain Injury, Vascular", "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?condition=Brain+Injury%2C+Vascular&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-06-10T18:51:32.035Z", "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": "NCT06169657", "title": "Comparison of Gait Training Methods in Sub-acute Stroke and Spinal Cord Injury", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Stroke", "Incomplete Spinal Cord Injury" ], "interventions": [ { "name": "Body-weight-supported treadmill training (BWSTT)", "type": "DEVICE" }, { "name": "EksoNR exoskeleton gait training", "type": "DEVICE" }, { "name": "Overground gait training", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Shirley Ryan AbilityLab", "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": 0, "start_date": "2024-09-01", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2025-05-25", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT06169657" }, { "nct_id": "NCT01990768", "title": "Prehospital Tranexamic Acid Use for Traumatic Brain Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Traumatic Brain Injury" ], "interventions": [ { "name": "1 gram Tranexamic Acid (TXA)", "type": "DRUG" }, { "name": "2 grams TXA", "type": "DRUG" }, { "name": "0.9% Sodium Chloride injectable", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Washington", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "15 Years", "maximum_age": null, "sex": "ALL", "summary": "15 Years and older" }, "enrollment_count": 967, "start_date": "2015-05", "completion_date": "2017-11-07", "has_results": true, "last_update_posted_date": "2019-01-14", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 10, "location_summary": "Birmingham, Alabama • Minneapolis, Minnesota • Rochester, Minnesota + 7 more", "locations": [ { "city": "Birmingham", "state": "Alabama" }, { "city": "Minneapolis", "state": "Minnesota" }, { "city": "Rochester", "state": "Minnesota" }, { "city": "Saint Paul", "state": "Minnesota" }, { "city": "Cincinnati", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT01990768" }, { "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": "2026-06-10T18:51:32.035Z", "location_count": 1, "location_summary": "Delafield, Wisconsin", "locations": [ { "city": "Delafield", "state": "Wisconsin" } ], "official_url": "https://clinicaltrials.gov/study/NCT04806620" }, { "nct_id": "NCT02052024", "title": "Myobloc Atrophy Study", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Spasticity Secondary to Either a Disorder or Trauma", "Spinal Cord Injury (SCI)", "Brain Injury", "Tumor", "Stroke" ], "interventions": [ { "name": "Botox", "type": "DRUG" }, { "name": "MYOBLOC", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Georgetown University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 10, "start_date": "2014-05", "completion_date": "2015-08", "has_results": false, "last_update_posted_date": "2015-12-16", "last_synced_at": "2026-06-10T18:51:32.035Z", "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/NCT02052024" }, { "nct_id": "NCT00070161", "title": "Phase II Studies Of Donepezil And Ginkgo Biloba In Irradiated Brain Tumor", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Brain and Central Nervous System Tumors", "Radiation Toxicity" ], "interventions": [ { "name": "EGb761", "type": "DIETARY_SUPPLEMENT" }, { "name": "donepezil hydrochloride", "type": "DRUG" }, { "name": "cognitive assessment", "type": "PROCEDURE" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "DRUG", "PROCEDURE" ], "sponsor": "Wake Forest University Health Sciences", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 68, "start_date": "2001-07-01", "completion_date": "2012-08-01", "has_results": false, "last_update_posted_date": "2021-09-09", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 4, "location_summary": "Phoenix, Arizona • Rome, Georgia • Winston-Salem, North Carolina + 1 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Rome", "state": "Georgia" }, { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Spartanburg", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT00070161" }, { "nct_id": "NCT04758052", "title": "Tracheostomy With Bedside Simultaneous Gastrostomy Vs Usual Care Tracheostomy And Delayed Gastrostomy Placement", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke, Acute", "TBI", "Neuromuscular Diseases", "Status Epilepticus", "Coma", "Cerebrovascular Disorders", "Spinal Cord Injuries", "Neurological Injury", "Neurologic Injury" ], "interventions": [ { "name": "Timing of placement", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "University of Mississippi Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 0, "start_date": "2021-03-31", "completion_date": "2022-08", "has_results": false, "last_update_posted_date": "2021-06-09", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 1, "location_summary": "Jackson, Mississippi", "locations": [ { "city": "Jackson", "state": "Mississippi" } ], "official_url": "https://clinicaltrials.gov/study/NCT04758052" }, { "nct_id": "NCT03598140", "title": "Sildenafil Treatment for Mild TBI", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Vascular System Injuries", "Concussion, Brain", "Post-Concussion Syndrome" ], "interventions": [ { "name": "Sildenafil Citrate", "type": "DRUG" }, { "name": "Placebo oral capsule", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Texas Southwestern Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "MALE", "summary": "18 Years to 35 Years · Male only" }, "enrollment_count": 22, "start_date": "2018-07-25", "completion_date": "2019-05-29", "has_results": true, "last_update_posted_date": "2020-11-19", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT03598140" }, { "nct_id": "NCT04916223", "title": "Study to Determine Therapeutic Massage Dosing to Improve Quality of Life in Hospitalized Patients Receiving Palliative Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cancer", "Heart Failure", "COPD", "Sepsis", "HIV Infections", "ESRD", "Trauma", "Stroke" ], "interventions": [ { "name": "Therapeutic massage", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Medstar Health Research Institute", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 405, "start_date": "2017-11-01", "completion_date": "2019-03-26", "has_results": false, "last_update_posted_date": "2022-12-13", "last_synced_at": "2026-06-10T18:51:32.035Z", "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/NCT04916223" }, { "nct_id": "NCT03743805", "title": "Rapid Reversal of CNS-Depressant Drug Effect Prior to Brain Death Determination", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Brain Death", "Anoxic Brain Injury", "Cardiac Arrest", "Sedative Intoxication", "Narcotic Intoxication" ], "interventions": [ { "name": "Flumazenil", "type": "DRUG" }, { "name": "Naloxone", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Prisma Health-Midlands", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2019-01-01", "completion_date": "2021-07-21", "has_results": false, "last_update_posted_date": "2024-10-31", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 1, "location_summary": "Columbia, South Carolina", "locations": [ { "city": "Columbia", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03743805" }, { "nct_id": "NCT01894802", "title": "Cortical Recording and Stimulating Array Brain-Machine Interface", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tetraplegia", "Spinal Cord Injury", "Brainstem Stroke", "Brachial Plexus Injury", "Above Elbow Amputation" ], "interventions": [ { "name": "Implantation of CRS Arrays", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Michael Boninger", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "22 Years to 70 Years" }, "enrollment_count": 30, "start_date": "2013-12-01", "completion_date": "2029-12", "has_results": false, "last_update_posted_date": "2026-05-20", "last_synced_at": "2026-06-10T18:51:32.035Z", "location_count": 2, "location_summary": "Chicago, Illinois • Pittsburgh, Pennsylvania", "locations": [ { "city": "Chicago", "state": "Illinois" }, { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT01894802" } ] }