{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?sponsor=John+D.+Dingell+VA+Medical+Center", "query": { "sponsor": "John D. Dingell VA Medical Center" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 11, "total_pages": 2, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?sponsor=John+D.+Dingell+VA+Medical+Center&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-10-11T18:48:31.801Z", "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": "NCT04615299", "title": "Battlefield Acupuncture and Its Use In Multimodal Perioperative Anesthesia Care", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acupuncture, Ear" ], "interventions": [ { "name": "Auricular acupuncture", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Anesthesiology WSU/DMC-NorthStar", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "100 Years", "sex": "ALL", "summary": "18 Years to 100 Years" }, "enrollment_count": 72, "start_date": "2018-06-06", "completion_date": "2019-06-06", "has_results": true, "last_update_posted_date": "2022-03-18", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT04615299" }, { "nct_id": "NCT00611871", "title": "The Use of Propranolol to Block Memory Reconsolidation in PTSD", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Posttraumatic Stress Disorders" ], "interventions": [ { "name": "Propranolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Wayne State University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "FEMALE", "summary": "18 Years to 45 Years · Female only" }, "enrollment_count": 12, "start_date": "2007-09", "completion_date": "2015-09", "has_results": false, "last_update_posted_date": "2016-11-01", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT00611871" }, { "nct_id": "NCT05351827", "title": "Mild Intermittent Hypoxia: A Prophylactic for Autonomic Dysfunction in Individuals With Spinal Cord Injuries", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Spinal Cord Injuries", "Autonomic Dysreflexia" ], "interventions": [ { "name": "Mild Intermittent Hypoxia", "type": "OTHER" }, { "name": "Sham", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "18 Years to 60 Years" }, "enrollment_count": 24, "start_date": "2022-10-01", "completion_date": "2027-10-29", "has_results": false, "last_update_posted_date": "2026-08-14", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05351827" }, { "nct_id": "NCT03462706", "title": "Quad Resection (Hot Snare vs Cold Snare vs Hot EMR vs Cold EMR)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colon Cancer", "Colon Polyp", "Colon Adenoma" ], "interventions": [ { "name": "Cold Snare", "type": "PROCEDURE" }, { "name": "Hot Snare", "type": "PROCEDURE" }, { "name": "Cold EMR", "type": "PROCEDURE" }, { "name": "Hot EMR", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Indiana University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 238, "start_date": "2018-02-06", "completion_date": "2021-05-14", "has_results": true, "last_update_posted_date": "2023-02-15", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT03462706" }, { "nct_id": "NCT07181811", "title": "Assessing the Effects of Ongoing Ocrelizumab (OCR) Therapy on Fatigue and Cognition in Veterans With Multiple Sclerosis", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Sclerosis" ], "interventions": [ { "name": "Multiple Sclerosis patients who have been on Ocrelizumab will undergo cognitive and fatigue assessments", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Anza Memon", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 30, "start_date": "2025-09-30", "completion_date": "2028-06-01", "has_results": false, "last_update_posted_date": "2025-09-18", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT07181811" }, { "nct_id": "NCT05589753", "title": "Sleep Disordered Breathing With Opioid Use", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Sleep Apnea", "Opioid Use", "Sleep Disordered Breathing" ], "interventions": [ { "name": "Hyperoxia", "type": "OTHER" }, { "name": "Acetazolamide", "type": "DRUG" } ], "intervention_types": [ "OTHER", "DRUG" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 150, "start_date": "2019-05-02", "completion_date": "2027-03-31", "has_results": false, "last_update_posted_date": "2026-07-01", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05589753" }, { "nct_id": "NCT02223299", "title": "Pilot Study: Combining Nutritional Supplements With Standard Antidepressant to Treat Depression.", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression" ], "interventions": [ { "name": "L-tyrosine", "type": "DIETARY_SUPPLEMENT" }, { "name": "L-Tryptophan", "type": "DIETARY_SUPPLEMENT" }, { "name": "deplin", "type": "DRUG" }, { "name": "Placebo A", "type": "OTHER" }, { "name": "Placebo B", "type": "OTHER" } ], "intervention_types": [ "DIETARY_SUPPLEMENT", "DRUG", "OTHER" ], "sponsor": "John D. Dingell VA Medical Center", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "18 Years to 65 Years" }, "enrollment_count": 0, "start_date": "2015-11", "completion_date": "2015-11", "has_results": false, "last_update_posted_date": "2020-02-21", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT02223299" }, { "nct_id": "NCT06462521", "title": "Cold Snare Piecemeal Resection vs Cold Snare Endoscopic Mucosal Resection", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Colon Cancer", "Colon Polyp", "Colon Adenoma", "Serrated Polyp" ], "interventions": [ { "name": "Cold Snare Piecemeal Resection (CSPR)", "type": "PROCEDURE" }, { "name": "Cold Snare Endoscopic Mucosal Resection (Cold EMR)", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "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": 570, "start_date": "2024-09-06", "completion_date": "2028-07", "has_results": false, "last_update_posted_date": "2025-12-30", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Indianapolis, Indiana", "locations": [ { "city": "Indianapolis", "state": "Indiana" } ], "official_url": "https://clinicaltrials.gov/study/NCT06462521" }, { "nct_id": "NCT05558501", "title": "Intermittent Hypoxia-initiated Plasticity in Humans: A Multi-pronged Therapeutic Approach to Treat Sleep Apnea and Overlapping Co-morbidities", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Obstructive Sleep Apnea" ], "interventions": [ { "name": "Mild Intermittent Hypoxia", "type": "OTHER" }, { "name": "Sham MIH", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "30 Years to 60 Years" }, "enrollment_count": 60, "start_date": "2023-01-01", "completion_date": "2027-12-31", "has_results": false, "last_update_posted_date": "2025-12-04", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05558501" }, { "nct_id": "NCT06291870", "title": "Predictors of Post-COVID-19 Clinical and Cognitive Consequences", "overall_status": "RECRUITING", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Post Acute Sequelae of SARS CoV 2 Infection", "Obstructive Sleep Apnea" ], "interventions": [], "intervention_types": [], "sponsor": "VA Office of Research and Development", "sponsor_class": "FED", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 200, "start_date": "2023-01-19", "completion_date": "2026-12-31", "has_results": false, "last_update_posted_date": "2026-01-23", "last_synced_at": "2026-10-11T18:48:31.801Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT06291870" } ] }