{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=low+threshold+care", "query": { "intervention": "low threshold care" }, "page_size": 10 }, "pagination": { "page": 1, "page_size": 10, "total_count": 27, "total_pages": 3, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=low+threshold+care&page=2&page_size=10", "previous_page_url": null }, "source": "remote", "last_synced_at": "2026-09-11T15:09:57.878Z", "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": "NCT06785376", "title": "P3 Trial: Estimating the Impact of a Multilevel, Multicomponent Intervention to Increase Uptake of HIV Testing and Biomedical HIV Prevention", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Testing", "PrEP Uptake" ], "interventions": [ { "name": "DIY (Do It Yourself)", "type": "BEHAVIORAL" }, { "name": "TRUST", "type": "BEHAVIORAL" }, { "name": "SOC", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Columbia University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "65 Years", "sex": "MALE", "summary": "18 Years to 65 Years · Male only" }, "enrollment_count": 480, "start_date": "2024-12-19", "completion_date": "2028-02-28", "has_results": false, "last_update_posted_date": "2026-08-31", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06785376" }, { "nct_id": "NCT04157400", "title": "Effect of Epidural Stimulation on Muscle Activation and Sensory Perception", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Pain" ], "interventions": [ { "name": "Intraoperative Parameter Testing", "type": "DEVICE" }, { "name": "Proprioception Testing During Stimulation", "type": "DEVICE" }, { "name": "Gait Analysis During Stimulation", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Medical University of South Carolina", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 5, "start_date": "2019-11-26", "completion_date": "2021-11-01", "has_results": true, "last_update_posted_date": "2023-02-15", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Charleston, South Carolina", "locations": [ { "city": "Charleston", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04157400" }, { "nct_id": "NCT07631598", "title": "Buprenorphine Implementation at Syringe Service Programs to Reduce Overdoses", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Opioid Use Disorder", "Opioid Use Disorder, Severe", "Opioid Use Disorder, Moderate" ], "interventions": [ { "name": "Standard of Care Referral", "type": "OTHER" }, { "name": "Low Threshold Buprenorphine", "type": "BEHAVIORAL" } ], "intervention_types": [ "OTHER", "BEHAVIORAL" ], "sponsor": "Montefiore Medical Center", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 512, "start_date": "2026-08-17", "completion_date": "2028-06", "has_results": false, "last_update_posted_date": "2026-08-21", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 8, "location_summary": "Los Angeles, California • Washington D.C., District of Columbia • Baton Rouge, Louisiana + 5 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Baton Rouge", "state": "Louisiana" }, { "city": "Duluth", "state": "Minnesota" }, { "city": "Roswell", "state": "New Mexico" } ], "official_url": "https://clinicaltrials.gov/study/NCT07631598" }, { "nct_id": "NCT06845774", "title": "The PROTECT (PrEP Optimization Through Telehealth Care and Treatment) Trial", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "HIV Prevention" ], "interventions": [ { "name": "CDC PrEP with active referral", "type": "BEHAVIORAL" }, { "name": "TelePrEP", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "Hilary L Surratt, PhD", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 80, "start_date": "2025-09-25", "completion_date": "2027-01-13", "has_results": false, "last_update_posted_date": "2026-05-15", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Lexington, Kentucky", "locations": [ { "city": "Lexington", "state": "Kentucky" } ], "official_url": "https://clinicaltrials.gov/study/NCT06845774" }, { "nct_id": "NCT06446739", "title": "LoW Dose-Intensity vs. Standard Dose-Intensity COntinuous Renal ReplaceMent Therapy in Critically Ill Patients (WISDOM)", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Kidney Injury", "Dialysis; Complications" ], "interventions": [ { "name": "Continuous Renal Replacement Therapy (CRRT)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Alberta", "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": "2024-11-14", "completion_date": "2027-06", "has_results": false, "last_update_posted_date": "2026-07-09", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT06446739" }, { "nct_id": "NCT07597239", "title": "Thromboelastography With Platelet Mapping to Guide Antiplatelet Therapy After Lower Extremity Revascularization", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Thrombosis", "Arterial Occlusive Diseases", "Thromboelastography (TEG)", "Peripheral Arterial Disease(PAD)", "Stent Thrombosis", "Platelet Inhibition", "PRU(Platelet Reactivity Unit)" ], "interventions": [ { "name": "Aspirin", "type": "DRUG" }, { "name": "Clopidogrel", "type": "DRUG" }, { "name": "Ticagrelor", "type": "DRUG" }, { "name": "Platelet Reactivity Testing", "type": "DIAGNOSTIC_TEST" }, { "name": "Thromboelastography with Platelet Mapping", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DRUG", "DIAGNOSTIC_TEST" ], "sponsor": "Massachusetts General Hospital", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "60 Years", "maximum_age": null, "sex": "ALL", "summary": "60 Years and older" }, "enrollment_count": 514, "start_date": "2020-11-01", "completion_date": "2026-10", "has_results": false, "last_update_posted_date": "2026-09-09", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Boston, Massachusetts", "locations": [ { "city": "Boston", "state": "Massachusetts" } ], "official_url": "https://clinicaltrials.gov/study/NCT07597239" }, { "nct_id": "NCT07737652", "title": "Microcurrent Neurofeedback as an Adjunct to Standard Care for Substance Use Disorders", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Depression", "Anxiety", "Substance Use Disorder (SUD)", "Post Traumatic Stress Disorder" ], "interventions": [ { "name": "Microcurrent Neurofeedback (MCN)", "type": "DEVICE" }, { "name": "Standard Care for Substance Use Disorder", "type": "BEHAVIORAL" } ], "intervention_types": [ "DEVICE", "BEHAVIORAL" ], "sponsor": "University of Alabama, Tuscaloosa", "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": 61, "start_date": "2025-10-06", "completion_date": "2026-06-30", "has_results": false, "last_update_posted_date": "2026-07-30", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Tuscaloosa, Alabama", "locations": [ { "city": "Tuscaloosa", "state": "Alabama" } ], "official_url": "https://clinicaltrials.gov/study/NCT07737652" }, { "nct_id": "NCT06474754", "title": "Submaximal Cardiopulmonary Exercise Testing for Detection of Myocardial Injury After Noncardiac Surgery", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Myocardial Injury After Non-cardiac Surgery", "Submaximal Exercise Performance", "Preoperative Period" ], "interventions": [ { "name": "High-sensitivity troponin, serum", "type": "DIAGNOSTIC_TEST" }, { "name": "Submaximal Cardiopulmonary Exercise Testing", "type": "DIAGNOSTIC_TEST" }, { "name": "Duke Activity Status Index", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Yale University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "45 Years", "maximum_age": null, "sex": "ALL", "summary": "45 Years and older" }, "enrollment_count": 10, "start_date": "2025-03-30", "completion_date": "2026-04-30", "has_results": false, "last_update_posted_date": "2026-05-22", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "New Haven, Connecticut", "locations": [ { "city": "New Haven", "state": "Connecticut" } ], "official_url": "https://clinicaltrials.gov/study/NCT06474754" }, { "nct_id": "NCT04564625", "title": "Relationships Between Vitamin D and Orthopedic Trauma", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Fracture", "Fracture Nonunion", "Fractures, Bone", "Vitamin D" ], "interventions": [ { "name": "Vitamin D Assessment", "type": "OTHER" }, { "name": "Fracture", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Methodist Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "25 Years", "sex": "ALL", "summary": "18 Years to 25 Years" }, "enrollment_count": 100, "start_date": "2020-03-06", "completion_date": "2021-02-26", "has_results": false, "last_update_posted_date": "2026-05-19", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04564625" }, { "nct_id": "NCT02919917", "title": "Treatment of Post-SCI Hypotension", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2", "PHASE3" ], "conditions": [ "Spinal Cord Injury", "Autonomic Dysreflexia", "Orthostatic Hypotension", "Baroreceptor Integrity", "Sympathetic Integrity", "Vagal Integrity", "Hypotension", "Cerebral Blood Flow", "Blood Pressure", "Venous Occlusion Plethysmography" ], "interventions": [ { "name": "Midodrine Hydrochloride", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "James J. Peters Veterans Affairs Medical Center", "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": 66, "start_date": "2017-06-01", "completion_date": "2021-09-01", "has_results": true, "last_update_posted_date": "2025-02-21", "last_synced_at": "2026-09-11T15:09:57.878Z", "location_count": 2, "location_summary": "New York, New York • The Bronx, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "The Bronx", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT02919917" } ] }