{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Electrical+Dysfunction", "query": { "condition": "Electrical Dysfunction" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 31, "total_pages": 4, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Electrical+Dysfunction&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-05T13:07:13.829Z", "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": "NCT03184792", "title": "Transcutaneous Electrical Spinal Stimulation to Restore Upper Extremity Functions in Spinal Cord Injury", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injury Cervical", "Upper Extremity Dysfunction" ], "interventions": [ { "name": "Transcutaneous spinal stimulation", "type": "DEVICE" }, { "name": "Physical therapy", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "University of Washington", "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": 15, "start_date": "2017-12-01", "completion_date": "2024-12-30", "has_results": true, "last_update_posted_date": "2025-11-04", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Seattle, Washington", "locations": [ { "city": "Seattle", "state": "Washington" } ], "official_url": "https://clinicaltrials.gov/study/NCT03184792" }, { "nct_id": "NCT04115540", "title": "Penile Nerve Stimulation for Treatment of Delayed Ejaculation", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Delayed Ejaculation" ], "interventions": [ { "name": "TENS penile nerve stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Stanford University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 20, "start_date": "2019-01-10", "completion_date": "2024-01-31", "has_results": true, "last_update_posted_date": "2025-03-20", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Stanford, California", "locations": [ { "city": "Stanford", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04115540" }, { "nct_id": "NCT06763549", "title": "COR-INSIGHT: Optimizing Cardiovascular and Cardiopulmonary Outcomes with AI-Driven Multiplexed Indications Using COR ECG Wearable", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Cardiopulmonary Failure", "Myocardial Infarction (MI)", "Heart Decompensation", "Heart Failure", "HFrEF - Heart Failure with Reduced Ejection Fraction", "HFpEF - Heart Failure with Preserved Ejection Fraction", "Syncopation", "Syncope", "Ischemic Cardiovascular Disease", "STEMI", "STEMI (ST Elevation MI)", "Atrial Fibrillation (AF)", "Atrial Enlargement", "LVF", "Conduction Defect", "Conduction Abnormalities", "Heart Block", "Valvular Diseases", "Cardiac Output, Low", "Stroke Volume", "Stroke Volume Variation", "Hyperkalemia", "Hypercalcemia", "Hypocalcemia", "LV Dysfunction", "QT Prolongation", "Sudden Cardiac Death Due to Cardiac Arrhythmia", "Ventricular Arrhythmia", "Pacing", "Pacing Induced Dyssynchrony", "Silent Ischemia", "Pericarditis", "Sleep Related Breathing Disorder", "RSA", "Apnea, Obstructive", "Cardiac Output Measurement", "Respiratory Impedance", "CRT And/or ICD", "Infarction", "Cardiomyopathies, Primary", "Hypertrophy" ], "interventions": [ { "name": "SUBPROTOCOL A", "type": "DEVICE" }, { "name": "SUBPROTOCOL B", "type": "DEVICE" }, { "name": "SUBPROTOCOL C", "type": "DEVICE" }, { "name": "SUBPROTOCOL D", "type": "DEVICE" }, { "name": "SUBPROTOCOL E", "type": "DEVICE" }, { "name": "SUBPROTOCOL F", "type": "DEVICE" }, { "name": "SUBPROTOCOL G", "type": "DEVICE" }, { "name": "SUBPROTOCOL H", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Peerbridge Health, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15000, "start_date": "2024-11-16", "completion_date": "2026-04-15", "has_results": false, "last_update_posted_date": "2025-01-08", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Melbourne, Florida", "locations": [ { "city": "Melbourne", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06763549" }, { "nct_id": "NCT07182058", "title": "Virtual tES Device Treatment for Parkinson's Disease Motor Symptoms", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "PARKINSON DISEASE (Disorder)" ], "interventions": [ { "name": "Transcranial Electrical Stimulation Device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "U: The Mind Company", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 30, "start_date": "2026-01-01", "completion_date": "2026-04-01", "has_results": false, "last_update_posted_date": "2026-01-27", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07182058" }, { "nct_id": "NCT04798378", "title": "NuroSleeve Powered Brace & Stimulation System to Restore Arm Function", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Neurologic Diseases", "Hemiparesis", "Quadriplegia", "Muscular Dystrophies", "Arthrogryposis", "Spinal Cord Injuries", "Charcot-Marie-Tooth", "Stroke", "Weakness of Extremities as Sequela of Stroke", "Weakness Due to Upper Motor Neuron Dysfunction", "Amyotrophic Lateral Sclerosis", "Spinal Muscular Atrophy", "Arm Paralysis", "Cerebral Palsy" ], "interventions": [ { "name": "Neurosleeve", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Thomas Jefferson University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "4 Years", "maximum_age": null, "sex": "ALL", "summary": "4 Years and older" }, "enrollment_count": 20, "start_date": "2020-04-16", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2025-04-09", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 2, "location_summary": "Wilmington, Delaware • Philadelphia, Pennsylvania", "locations": [ { "city": "Wilmington", "state": "Delaware" }, { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04798378" }, { "nct_id": "NCT06699056", "title": "AI-Enabled Direct-from-ECG Ejection Fraction (EF) Severity Assessment Using COR ECG Wearable Monitor", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ventricular Ejection Fraction", "LVF", "LV Dysfunction", "Atrial Enlargement", "Conduction Defect", "Heart Failure", "Valvular Heart Disease", "Ischemic Heart Disease", "Cardiotoxicity", "Myocardial Infarction", "Dilated Cardiomyopathy", "HFrEF - Heart Failure With Reduced Ejection Fraction", "HFpEF - Heart Failure With Preserved Ejection Fraction", "Syncope", "Remodeling, Cardiac" ], "interventions": [ { "name": "15-minutes of sitting during COR ECG Acquistion", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Peerbridge Health, Inc", "sponsor_class": "INDUSTRY", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2000, "start_date": "2024-11-21", "completion_date": "2027-11-15", "has_results": false, "last_update_posted_date": "2026-06-01", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 8, "location_summary": "Orange, California • Pasadena, California • Detroit, Michigan + 5 more", "locations": [ { "city": "Orange", "state": "California" }, { "city": "Pasadena", "state": "California" }, { "city": "Detroit", "state": "Michigan" }, { "city": "Hackensack", "state": "New Jersey" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06699056" }, { "nct_id": "NCT04466228", "title": "Non-invasive Transcranial Electrical Stimulation in MS", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Sclerosis", "Cognitive Impairment" ], "interventions": [ { "name": "non-invasive transcranial electrical stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Francisco", "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": 60, "start_date": "2020-10-16", "completion_date": "2022-08-23", "has_results": true, "last_update_posted_date": "2023-12-04", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04466228" }, { "nct_id": "NCT06836739", "title": "At-Home Genital Nerve Stimulation for SCI Bowel", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injury" ], "interventions": [ { "name": "Genital nerve stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "MetroHealth Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12, "start_date": "2025-03-01", "completion_date": "2026-09-30", "has_results": false, "last_update_posted_date": "2026-07-28", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT06836739" }, { "nct_id": "NCT01446965", "title": "Vest Prevention of Early Sudden Death Trial and VEST Registry", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Myocardial Infarction", "Ventricular Dysfunction", "Sudden Death", "Ventricular Tachycardia", "Ventricular Fibrillation" ], "interventions": [ { "name": "wearable defibrillator", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 2348, "start_date": "2008-07", "completion_date": "2019-05-31", "has_results": true, "last_update_posted_date": "2021-01-20", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 57, "location_summary": "Anchorage, Alaska • Fresno, California • Salinas, California + 47 more", "locations": [ { "city": "Anchorage", "state": "Alaska" }, { "city": "Fresno", "state": "California" }, { "city": "Salinas", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT01446965" }, { "nct_id": "NCT00508521", "title": "Treatment of Hand Dysfunction After Stroke", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stroke" ], "interventions": [ { "name": "Functional Electrical Stimulation", "type": "DEVICE" }, { "name": "Standard Care", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "US Department of Veterans Affairs", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 4, "start_date": "2007-01", "completion_date": "2010-06", "has_results": true, "last_update_posted_date": "2014-02-07", "last_synced_at": "2026-09-05T13:07:13.829Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT00508521" } ] }