{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=There+is+no+intervention+for+this+study", "query": { "intervention": "There is no intervention for this study" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 302, "total_pages": 31, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=There+is+no+intervention+for+this+study&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-23T23:02:00.355Z", "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": "NCT05877417", "title": "Blood Flow Restriction and Creatine Supplementation in Women", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Physical Inactivity" ], "interventions": [ { "name": "Creatine Monohydrate", "type": "DIETARY_SUPPLEMENT" }, { "name": "Blood Flow Restriction", "type": "DEVICE" }, { "name": "Exercise", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "DEVICE", "OTHER" ], "sponsor": "University of Central Florida", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "35 Years", "sex": "FEMALE", "summary": "18 Years to 35 Years · Female only" }, "enrollment_count": 68, "start_date": "2023-05-17", "completion_date": "2024-03-01", "has_results": false, "last_update_posted_date": "2024-06-12", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Orlando, Florida", "locations": [ { "city": "Orlando", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT05877417" }, { "nct_id": "NCT00393874", "title": "Efficacy of Sleep Interventions for Posttraumatic Stress Disorder (PTSD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anxiety Disorders", "Mood Disorders", "Insomnia", "Nightmares" ], "interventions": [ { "name": "Behavioral Sleep Intervention", "type": "BEHAVIORAL" }, { "name": "Prazosin", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "BEHAVIORAL", "DRUG" ], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "18 Years to 55 Years" }, "enrollment_count": 50, "start_date": "2006-10", "completion_date": "2011-06", "has_results": true, "last_update_posted_date": "2016-10-24", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00393874" }, { "nct_id": "NCT04370002", "title": "Sensor-based Characterization of Depression", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Unipolar Depression" ], "interventions": [], "intervention_types": [], "sponsor": "Massachusetts General Hospital", "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": 100, "start_date": "2020-01-28", "completion_date": "2024-11-30", "has_results": false, "last_update_posted_date": "2023-11-03", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 2, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT04370002" }, { "nct_id": "NCT04100486", "title": "Non-Invasive Bioelectronic Analytics", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Autonomic Dysfunction", "Autonomic Imbalance", "Autonomic Nervous System Diseases", "Vagus Nerve Autonomic Disorder" ], "interventions": [ { "name": "Standing-Squatting-Standing Test", "type": "OTHER" }, { "name": "Deep Breathing Test", "type": "OTHER" }, { "name": "Cold Pressor Test", "type": "OTHER" }, { "name": "Cold Face Test", "type": "OTHER" }, { "name": "Valsalva Maneuver", "type": "OTHER" }, { "name": "Transcutaneous Auricular Vagus Nerve Stimulation (taVNS)", "type": "DEVICE" } ], "intervention_types": [ "OTHER", "DEVICE" ], "sponsor": "Northwell Health", "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": 48, "start_date": "2019-08-29", "completion_date": "2027-07", "has_results": false, "last_update_posted_date": "2026-06-09", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Manhasset, New York", "locations": [ { "city": "Manhasset", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04100486" }, { "nct_id": "NCT07092293", "title": "Studying Rehabilitation Treatments Using Video to Improve Recovery for Adults With Physical Disabilities", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Stroke", "Spinal Cord Injury", "Occupational Therapy" ], "interventions": [ { "name": "occupational therapy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Ohio State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 56, "start_date": "2025-02-11", "completion_date": "2026-06-10", "has_results": false, "last_update_posted_date": "2026-07-06", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Columbus, Ohio", "locations": [ { "city": "Columbus", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07092293" }, { "nct_id": "NCT04213651", "title": "A Non-Interventional Pilot Study to Explore the Role of Gut Flora in Diabetes Mellitus", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Diabetes Mellitus", "Diabetes Mellitus, Type 2" ], "interventions": [ { "name": "No intervention", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "ProgenaBiome", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 0, "start_date": "2020-03-02", "completion_date": "2030-07", "has_results": false, "last_update_posted_date": "2025-06-05", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Ventura, California", "locations": [ { "city": "Ventura", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT04213651" }, { "nct_id": "NCT04142177", "title": "Sequential and Comparative Evaluation of Pain Treatment Effectiveness Response", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Low Back Pain" ], "interventions": [ { "name": "Pain EASE", "type": "OTHER" }, { "name": "Tailored exercise", "type": "PROCEDURE" }, { "name": "Continued Care and Active Monitoring", "type": "OTHER" }, { "name": "Cognitive Behavioral Therapy (CBT)", "type": "BEHAVIORAL" }, { "name": "Spinal Manipulation Therapy (SMT)", "type": "PROCEDURE" }, { "name": "Yoga", "type": "PROCEDURE" } ], "intervention_types": [ "OTHER", "PROCEDURE", "BEHAVIORAL" ], "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": 2529, "start_date": "2022-06-13", "completion_date": "2027-06-30", "has_results": false, "last_update_posted_date": "2026-05-04", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 19, "location_summary": "Phoenix, Arizona • Loma Linda, California • Long Beach, California + 16 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Loma Linda", "state": "California" }, { "city": "Long Beach", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "Aurora", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT04142177" }, { "nct_id": "NCT07361328", "title": "Personalized Ultrasonic Brain Stimulation for Fibromyalgia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Fibromyalgia (FM)" ], "interventions": [ { "name": "Low-intensity ultrasound brain stimulation", "type": "DEVICE" }, { "name": "Sham (No Treatment)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Utah", "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": 50, "start_date": "2026-01-05", "completion_date": "2028-12-31", "has_results": false, "last_update_posted_date": "2026-01-23", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Salt Lake City, Utah", "locations": [ { "city": "Salt Lake City", "state": "Utah" } ], "official_url": "https://clinicaltrials.gov/study/NCT07361328" }, { "nct_id": "NCT04776304", "title": "Art Therapy QEEG Study for Service Members with a Traumatic Brain Injury and Posttraumatic Stress Symptoms", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Post-Traumatic Headache", "PTSD", "TBI", "TBI (Traumatic Brain Injury)", "MTBI - Mild Traumatic Brain Injury", "Posttraumatic Stress Disorder", "Posttraumatic Stress Disorder, Delayed Onset", "Sleep Disturbance", "Nightmare", "Nightmares, REM-Sleep Type", "Headache", "Irritable Mood", "Anger", "Eating Disorders", "Combat and Operational Stress Reaction", "Combat Stress Disorders", "Military Operations", "Military Activity", "Military Family" ], "interventions": [ { "name": "Art Therapy", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Walter Reed National Military Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "64 Years", "sex": "ALL", "summary": "18 Years to 64 Years" }, "enrollment_count": 2, "start_date": "2021-10-30", "completion_date": "2024-01-25", "has_results": false, "last_update_posted_date": "2024-11-06", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT04776304" }, { "nct_id": "NCT01392209", "title": "Hypofractionated Stereotactic Radiotherapy With Bevacizumab in the Treatment of Recurrent Malignant Glioma", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Brain Cancer", "MALIGNANT GLIOMA", "Glioblastoma", "Anaplastic Astrocytoma (AA)", "Anaplastic Oligodendroglioma (AO)", "Anaplastic Oligo-astrocytoma (AOA)", "Anaplastic Mixed Gliomas", "Malignant Glioma NOS" ], "interventions": [ { "name": "Bevacizumab & Stereotactic Radiotherapy", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Memorial Sloan Kettering Cancer Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 15, "start_date": "2011-07-08", "completion_date": "2019-11-15", "has_results": false, "last_update_posted_date": "2019-11-22", "last_synced_at": "2026-09-23T23:02:00.355Z", "location_count": 5, "location_summary": "San Francisco, California • Basking Ridge, New Jersey • Commack, New York + 2 more", "locations": [ { "city": "San Francisco", "state": "California" }, { "city": "Basking Ridge", "state": "New Jersey" }, { "city": "Commack", "state": "New York" }, { "city": "Harrison", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01392209" } ] }