{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Propranolol+Pill&page=2", "query": { "intervention": "Propranolol Pill", "page": 2 }, "page_size": 10 }, "pagination": { "page": 2, "page_size": 10, "total_count": 10, "total_pages": 1, "next_page_url": null, "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Propranolol+Pill&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-26T09:38:44.697Z", "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": "NCT00262470", "title": "Treatment of Orthostatic Intolerance", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE1", "PHASE2" ], "conditions": [ "Tachycardia", "Chronic Orthostatic Intolerance" ], "interventions": [ { "name": "Acetazolamide", "type": "DRUG" }, { "name": "Atomoxetine", "type": "DRUG" }, { "name": "NO Drug", "type": "OTHER" }, { "name": "Clonidine", "type": "DRUG" }, { "name": "Entacapone", "type": "DRUG" }, { "name": "Entacapone & Propranolol", "type": "DRUG" }, { "name": "Atomoxetine & Propranolol", "type": "DRUG" }, { "name": "Indomethacin", "type": "DRUG" }, { "name": "Mecamylamine", "type": "DRUG" }, { "name": "Isosorbide Dinitrate", "type": "DRUG" }, { "name": "Melatonin", "type": "DIETARY_SUPPLEMENT" }, { "name": "Midodrine", "type": "DRUG" }, { "name": "Modafinil", "type": "DRUG" }, { "name": "Octreotide", "type": "DRUG" }, { "name": "Placebo", "type": "RADIATION" }, { "name": "Propranolol", "type": "DRUG" }, { "name": "Modafinil & Propranolol", "type": "DRUG" }, { "name": "Sertraline", "type": "DRUG" }, { "name": "IV Saline", "type": "PROCEDURE" }, { "name": "Drinking Water", "type": "OTHER" }, { "name": "Breathing Device", "type": "DEVICE" }, { "name": "memantine", "type": "DRUG" }, { "name": "Abdominal binder", "type": "DEVICE" } ], "intervention_types": [ "DRUG", "OTHER", "DIETARY_SUPPLEMENT", "RADIATION", "PROCEDURE", "DEVICE" ], "sponsor": "Satish R. Raj", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 150, "start_date": "1997-04", "completion_date": "2029-12", "has_results": false, "last_update_posted_date": "2025-10-08", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Nashville, Tennessee", "locations": [ { "city": "Nashville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT00262470" }, { "nct_id": "NCT04421209", "title": "Analgesic Effects of Perioperative Propranolol Administration for Spine Surgery", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Lumbar Disc Disease", "Spinal Fusion", "Degenerative Disc Disease" ], "interventions": [ { "name": "Propranolol Hcl 40mg Tab", "type": "DRUG" }, { "name": "Placebo oral tablet", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Duke University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2020-12", "completion_date": "2021-09-30", "has_results": false, "last_update_posted_date": "2021-03-16", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT04421209" }, { "nct_id": "NCT07271485", "title": "Propranolol for Misophonia", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Misophonia", "Propanolol", "Misophonia Treatment" ], "interventions": [ { "name": "propranolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Bloom Mental Health, LLC", "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": 20, "start_date": "2025-12-19", "completion_date": "2026-12-19", "has_results": false, "last_update_posted_date": "2025-12-09", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Littleton, Colorado", "locations": [ { "city": "Littleton", "state": "Colorado" } ], "official_url": "https://clinicaltrials.gov/study/NCT07271485" }, { "nct_id": "NCT00934947", "title": "Burn Healing and Analgesia With Propranolol", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Burns", "Pain" ], "interventions": [ { "name": "Propranolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" }, { "name": "Propanolol", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "59 Years", "sex": "ALL", "summary": "18 Years to 59 Years" }, "enrollment_count": 45, "start_date": "2009-07", "completion_date": "2011-06", "has_results": true, "last_update_posted_date": "2017-11-17", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 4, "location_summary": "Washington D.C., District of Columbia • Chapel Hill, North Carolina • Wake Forest, North Carolina + 1 more", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Chapel Hill", "state": "North Carolina" }, { "city": "Wake Forest", "state": "North Carolina" }, { "city": "Upland", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00934947" }, { "nct_id": "NCT02437383", "title": "Study of Orofacial Pain and PropRANOlol", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Temporomandibular Disorders" ], "interventions": [ { "name": "Propranolol ER", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of North Carolina, Chapel Hill", "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": 200, "start_date": "2015-08-20", "completion_date": "2018-04-25", "has_results": true, "last_update_posted_date": "2019-05-21", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 3, "location_summary": "Gainesville, Florida • Buffalo, New York • Chapel Hill, North Carolina", "locations": [ { "city": "Gainesville", "state": "Florida" }, { "city": "Buffalo", "state": "New York" }, { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02437383" }, { "nct_id": "NCT06263452", "title": "Beta-Blocker Influences on Inflammatory and Neural Responses to Stress", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Cardiovascular Disease" ], "interventions": [ { "name": "Propranolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of North Carolina, Chapel Hill", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "30 Years", "sex": "ALL", "summary": "18 Years to 30 Years" }, "enrollment_count": 120, "start_date": "2024-05-01", "completion_date": "2026-05", "has_results": false, "last_update_posted_date": "2025-10-29", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT06263452" }, { "nct_id": "NCT01077921", "title": "Study of Propranolol as Anti-Adhesive Therapy in Sickle Cell Disease (SCD)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Sickle Cell Disease" ], "interventions": [ { "name": "Propranolol", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Laura M. De Castro, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 31, "start_date": "2010-06", "completion_date": "2013-12", "has_results": true, "last_update_posted_date": "2015-01-22", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Durham, North Carolina", "locations": [ { "city": "Durham", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT01077921" }, { "nct_id": "NCT01791114", "title": "The Effect of Brown Adipose Tissue Activation on Insulin Sensitivity in Humans", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Insulin Sensitivity", "Obesity" ], "interventions": [ { "name": "Cold exposure", "type": "OTHER" }, { "name": "Cold exposure plus propranolol", "type": "OTHER" }, { "name": "Thermoneutral Conditions", "type": "OTHER" }, { "name": "Cold water consumption", "type": "OTHER" }, { "name": "Tepid water consumption", "type": "OTHER" }, { "name": "Exercise", "type": "OTHER" }, { "name": "Meal consumption", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Rutgers University", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "75 Years", "sex": "ALL", "summary": "18 Years to 75 Years" }, "enrollment_count": 39, "start_date": "2012-01", "completion_date": "2018-12-30", "has_results": false, "last_update_posted_date": "2021-03-16", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Galveston, Texas", "locations": [ { "city": "Galveston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT01791114" }, { "nct_id": "NCT05256069", "title": "Sex-related Differences in Sympathetic Vascular Transduction in the Setting of Hypoxemia", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Vasodilation", "Hypoxia" ], "interventions": [ { "name": "Propranolol Pill", "type": "DRUG" }, { "name": "Placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "University of Missouri-Columbia", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "45 Years", "sex": "ALL", "summary": "18 Years to 45 Years" }, "enrollment_count": 31, "start_date": "2023-04-26", "completion_date": "2025-07-31", "has_results": false, "last_update_posted_date": "2025-09-15", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Columbia, Missouri", "locations": [ { "city": "Columbia", "state": "Missouri" } ], "official_url": "https://clinicaltrials.gov/study/NCT05256069" }, { "nct_id": "NCT02972554", "title": "Does Propranolol Attenuate Inflammatory Responses to a Psychological Stressor?", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Stress, Psychological", "Inflammation", "Cortisol", "Sympathetic Nervous System" ], "interventions": [ { "name": "Propanolol hydrochloride", "type": "DRUG" }, { "name": "Placebo", "type": "OTHER" } ], "intervention_types": [ "DRUG", "OTHER" ], "sponsor": "University of North Carolina, Chapel Hill", "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": 92, "start_date": "2016-01-26", "completion_date": "2017-10-10", "has_results": true, "last_update_posted_date": "2018-12-19", "last_synced_at": "2026-09-26T09:38:44.697Z", "location_count": 1, "location_summary": "Chapel Hill, North Carolina", "locations": [ { "city": "Chapel Hill", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT02972554" } ] }