{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Population+Management+System&page=20", "query": { "intervention": "Population Management System", "page": 20 }, "page_size": 10 }, "pagination": { "page": 20, "page_size": 10, "total_count": 707, "total_pages": 71, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Population+Management+System&page=21&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Population+Management+System&page=19&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-22T12:43:00.539Z", "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": "NCT06543316", "title": "Marginal Ulcer Healing With Low-Thermal Argon Plasma Endoscopic Treatment", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Roux-en-y Anastomosis Site", "Marginal Ulcer", "Marginal Ulcer (Peptic) or Erosion", "Ulcer", "Ulcer, Gastric", "Ulcer Gastrointestinal", "Abdominal Pain", "Nausea", "Vomiting", "GastroIntestinal Bleeding", "Dysphagia", "Ulcer Gastrojejunal" ], "interventions": [ { "name": "Low Thermal Plasma (LTP) Treatment", "type": "PROCEDURE" }, { "name": "Standard of Care Ulcer Treatment (typically PPI Administration)", "type": "OTHER" } ], "intervention_types": [ "PROCEDURE", "OTHER" ], "sponsor": "Christopher C. Thompson, MD, MSc", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2025-03-04", "completion_date": "2028-06", "has_results": false, "last_update_posted_date": "2026-06-25", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT06543316" }, { "nct_id": "NCT04826133", "title": "Vitamin D and Cocaine Administration", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Cocaine Use Disorder" ], "interventions": [ { "name": "Calcitriol", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "30 Years", "maximum_age": "55 Years", "sex": "ALL", "summary": "30 Years to 55 Years" }, "enrollment_count": 4, "start_date": "2019-03-27", "completion_date": "2020-01-17", "has_results": false, "last_update_posted_date": "2023-08-14", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT04826133" }, { "nct_id": "NCT01812447", "title": "Evaluation of the Spiration® Valve System for Emphysema to Improve Lung Function", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Emphysema" ], "interventions": [ { "name": "Spiration Valve System", "type": "DEVICE" }, { "name": "Medical Management", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER" ], "sponsor": "Olympus Corporation of the Americas", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": null, "sex": "ALL", "summary": "40 Years and older" }, "enrollment_count": 172, "start_date": "2013-06", "completion_date": "2022-08", "has_results": false, "last_update_posted_date": "2024-05-31", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 32, "location_summary": "Fort Smith, Arkansas • Riverside, California • San Diego, California + 28 more", "locations": [ { "city": "Fort Smith", "state": "Arkansas" }, { "city": "Riverside", "state": "California" }, { "city": "San Diego", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01812447" }, { "nct_id": "NCT02346734", "title": "Physical Telerehabilitation in Veterans With Multiple Sclerosis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Multiple Sclerosis" ], "interventions": [ { "name": "Multiple Sclerosis Home Automated Telemanagement (MS HAT) system", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Maryland, Baltimore", "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": 51, "start_date": "2012-07", "completion_date": "2017-04-06", "has_results": true, "last_update_posted_date": "2026-05-05", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT02346734" }, { "nct_id": "NCT01008527", "title": "Phase I Oncovir Poly IC:LC and NY-ESO-1/gp100", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1" ], "conditions": [ "Melanoma" ], "interventions": [ { "name": "CP 870,893", "type": "DRUG" }, { "name": "Peptides", "type": "BIOLOGICAL" }, { "name": "Oncovir poly IC:LC", "type": "BIOLOGICAL" } ], "intervention_types": [ "DRUG", "BIOLOGICAL" ], "sponsor": "H. Lee Moffitt Cancer Center and 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": 22, "start_date": "2009-10", "completion_date": "2015-09", "has_results": false, "last_update_posted_date": "2015-09-24", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "Tampa, Florida", "locations": [ { "city": "Tampa", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01008527" }, { "nct_id": "NCT02529618", "title": "Field Implementation of iDETECT", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Concussion", "Brain Trauma" ], "interventions": [ { "name": "integrated Display Enhanced Testing for Cognitive Impairment and mild traumatic brain injury (iDETECT)", "type": "DEVICE" }, { "name": "Riddell High Impact Technology (HIT) System", "type": "DEVICE" }, { "name": "i1 Biometrics Vector Mouth Guard", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Emory University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "14 Years", "maximum_age": null, "sex": "ALL", "summary": "14 Years and older" }, "enrollment_count": 124, "start_date": "2015-08", "completion_date": "2016-02", "has_results": false, "last_update_posted_date": "2016-03-04", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 4, "location_summary": "Atlanta, Georgia • College Park, Georgia • Marietta, Georgia + 1 more", "locations": [ { "city": "Atlanta", "state": "Georgia" }, { "city": "College Park", "state": "Georgia" }, { "city": "Marietta", "state": "Georgia" }, { "city": "Roswell", "state": "Georgia" } ], "official_url": "https://clinicaltrials.gov/study/NCT02529618" }, { "nct_id": "NCT01073020", "title": "Surgery or Lifestyle With Intensive Medical Management in the Treatment of Type 2 Diabetes", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Type 2 Diabetes Mellitus", "Obesity" ], "interventions": [ { "name": "Allergan Adjustable Gastric Band Surgery", "type": "DEVICE" }, { "name": "Intensive Medical Diabetes & Weight Management (Why WAIT) - Band Group", "type": "OTHER" }, { "name": "Roux-en-Y Gastric Bypass (RYGB) Surgery", "type": "PROCEDURE" }, { "name": "Intensive Medical Diabetes & Weight Management (Why WAIT) - Bypass Group", "type": "OTHER" } ], "intervention_types": [ "DEVICE", "OTHER", "PROCEDURE" ], "sponsor": "Joslin Diabetes Center", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": "65 Years", "sex": "ALL", "summary": "21 Years to 65 Years" }, "enrollment_count": 88, "start_date": "2010-01", "completion_date": "2016-11", "has_results": true, "last_update_posted_date": "2021-06-28", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 2, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" }, { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT01073020" }, { "nct_id": "NCT07474090", "title": "Personalized Exercise Program for Survivors of Breast Cancer, STEPS-BC Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Anatomic Stage I Breast Cancer AJCC v8", "Anatomic Stage II Breast Cancer AJCC v8", "Anatomic Stage III Breast Cancer AJCC v8", "Breast Carcinoma", "Breast Inflammatory Carcinoma", "Locally Recurrent Breast Carcinoma" ], "interventions": [ { "name": "Exercise Intervention", "type": "OTHER" }, { "name": "Educational Intervention", "type": "OTHER" }, { "name": "Supportive Care", "type": "OTHER" }, { "name": "Biospecimen Collection", "type": "PROCEDURE" }, { "name": "Magnetic Resonance Imaging", "type": "PROCEDURE" }, { "name": "Questionnaire Administration", "type": "OTHER" }, { "name": "Accelerometry", "type": "PROCEDURE" }, { "name": "Electronic Health Record Review", "type": "OTHER" }, { "name": "Cardiopulmonary Exercise Testing", "type": "OTHER" } ], "intervention_types": [ "OTHER", "PROCEDURE" ], "sponsor": "Wake Forest University Health Sciences", "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": 120, "start_date": "2026-10-02", "completion_date": "2030-04-30", "has_results": false, "last_update_posted_date": "2026-10-06", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 4, "location_summary": "Winston-Salem, North Carolina • Richmond, Virginia", "locations": [ { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Winston-Salem", "state": "North Carolina" }, { "city": "Richmond", "state": "Virginia" }, { "city": "Richmond", "state": "Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT07474090" }, { "nct_id": "NCT02856412", "title": "Improving Mind/Body Health and Functioning With Integrative Exercise", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Stress Disorders, Post-Traumatic" ], "interventions": [ { "name": "Veterans Group Exercise (VGX)", "type": "OTHER" }, { "name": "Illness Management and Recovery", "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": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 84, "start_date": "2017-09-04", "completion_date": "2023-02-01", "has_results": true, "last_update_posted_date": "2024-09-19", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "San Francisco, California", "locations": [ { "city": "San Francisco", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT02856412" }, { "nct_id": "NCT04791761", "title": "Non-Opioid Pain Medications After Intracapsular Adenotonsillectomy", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Adenotonsillectomy", "Post-operative Analgesia", "Opioid Use" ], "interventions": [ { "name": "Oxycodone", "type": "DRUG" }, { "name": "Ibuprofen", "type": "DRUG" }, { "name": "Acetaminophen", "type": "DRUG" }, { "name": "Opioid disposal pouch", "type": "OTHER" }, { "name": "Opioid disposal education", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "David Chi, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "3 Years", "maximum_age": "17 Years", "sex": "ALL", "summary": "3 Years to 17 Years" }, "enrollment_count": 73, "start_date": "2021-04-13", "completion_date": "2023-07-03", "has_results": true, "last_update_posted_date": "2024-08-30", "last_synced_at": "2026-10-22T12:43:00.539Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04791761" } ] }