{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Angioplasty&page=2", "query": { "condition": "Angioplasty", "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?condition=Angioplasty&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-06-26T04:37:25.190Z", "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": "NCT00631540", "title": "REFORM Clinical Study: Treatment of Renal Artery Stenosis With the Formula Balloon-Expandable Stent", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Renal Artery Stenosis" ], "interventions": [ { "name": "Formula Balloon-Expandable Stent", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Cook Group Incorporated", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 100, "start_date": "2008-02", "completion_date": "2012-05", "has_results": true, "last_update_posted_date": "2013-12-16", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 7, "location_summary": "Ocala, Florida • Orlando, Florida • New York, New York + 4 more", "locations": [ { "city": "Ocala", "state": "Florida" }, { "city": "Orlando", "state": "Florida" }, { "city": "New York", "state": "New York" }, { "city": "Raleigh", "state": "North Carolina" }, { "city": "Lancaster", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT00631540" }, { "nct_id": "NCT00714623", "title": "The SCRIPPS DES REAL WORLD Registry", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Coronary Artery Disease", "Coronary Restenosis", "Coronary Thrombosis" ], "interventions": [ { "name": "Sirolimus-Eluting Bx Velocity Coronary Stent (CypherTM Sirolimus-Eluting Stent)", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Paul S Teirstein, MD", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 859, "start_date": "2005-03", "completion_date": "2012-04", "has_results": false, "last_update_posted_date": "2012-12-24", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 1, "location_summary": "La Jolla, California", "locations": [ { "city": "La Jolla", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT00714623" }, { "nct_id": "NCT01742117", "title": "Tailored Antiplatelet Therapy Following PCI", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Coronary Artery Disease", "Acute Coronary Syndrome", "Stenosis" ], "interventions": [ { "name": "Clopidogrel", "type": "DRUG" }, { "name": "Ticagrelor", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 5276, "start_date": "2013-05", "completion_date": "2020-10-31", "has_results": true, "last_update_posted_date": "2021-11-09", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 26, "location_summary": "Scottsdale, Arizona • San Diego, California • San Francisco, California + 20 more", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "San Diego", "state": "California" }, { "city": "San Francisco", "state": "California" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Naples", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT01742117" }, { "nct_id": "NCT00911976", "title": "Study of the Xience V Everolimus-eluting Stent in Saphenous Vein Graft Lesions", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Coronary Artery Bypass", "Atherosclerosis" ], "interventions": [ { "name": "Xience V coronary stent", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "North Texas Veterans Healthcare System", "sponsor_class": "FED", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 40, "start_date": "2009-05", "completion_date": "2011-07", "has_results": false, "last_update_posted_date": "2012-10-26", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 1, "location_summary": "Dallas, Texas", "locations": [ { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00911976" }, { "nct_id": "NCT01500902", "title": "Prediction of Cardiovascular Events in Vulnerable Patients Following Acute Coronary Syndrome", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Acute Coronary Syndrome" ], "interventions": [ { "name": "EndoPAT testing (non invasive device)", "type": "OTHER" }, { "name": "WatchPAT testing (non-invasive device)", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 101, "start_date": "2011-09", "completion_date": "2015-04", "has_results": false, "last_update_posted_date": "2015-09-23", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT01500902" }, { "nct_id": "NCT04433572", "title": "Temsirolimus Adventitial Delivery to Improve ANGioplasty and/or Atherectomy Revascularization Outcomes Below the Knee", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Peripheral Artery Disease", "Critical Limb Ischemia" ], "interventions": [ { "name": "Temsirolimus", "type": "DRUG" }, { "name": "Saline placebo", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Mercator MedSystems, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 250, "start_date": "2025-07-30", "completion_date": "2032-08-01", "has_results": false, "last_update_posted_date": "2025-08-05", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 2, "location_summary": "Houma, Louisiana • Dallas, Texas", "locations": [ { "city": "Houma", "state": "Louisiana" }, { "city": "Dallas", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT04433572" }, { "nct_id": "NCT00133731", "title": "The SEPIA-PCI Trial: Otamixaban in Comparison to Heparin in Subjects Undergoing Non-Urgent Percutaneous Coronary Intervention", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Angioplasty, Transluminal, Percutaneous Coronary" ], "interventions": [ { "name": "Otamixaban (XRP0673)", "type": "DRUG" }, { "name": "Unfractionated Heparin", "type": "DRUG" }, { "name": "Percutaneous Coronary Intervention", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "PROCEDURE" ], "sponsor": "Sanofi", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 947, "start_date": "2004-09", "completion_date": "2005-10", "has_results": false, "last_update_posted_date": "2008-07-02", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 37, "location_summary": "Los Angeles, California • Santa Ana, California • Washington D.C., District of Columbia + 31 more", "locations": [ { "city": "Los Angeles", "state": "California" }, { "city": "Santa Ana", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Atlantis", "state": "Florida" }, { "city": "Ocala", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT00133731" }, { "nct_id": "NCT01593891", "title": "Radiographic and Intravascular (IVUS) Evaluation of Venous Morphology During CCSVI Treatment", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "To Determine the Safety and Validity of Venous Angioplasty and", "Valvuloplasty in the Treatment of CCSVI. In Addition, it Will", "Allow Researchers to Sub-classify Valve Morphology in Relation", "to Treatment Success. This Will be Evidenced by Venous Patency", "Forty-eight Hours by Doppler Ultrasound as Well as Clinical", "Symptom Improvement." ], "interventions": [], "intervention_types": [], "sponsor": "Synergy Health Concepts, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "20 Years", "maximum_age": "60 Years", "sex": "ALL", "summary": "20 Years to 60 Years" }, "enrollment_count": 45, "start_date": "2011-08", "completion_date": "2012-09", "has_results": false, "last_update_posted_date": "2012-05-08", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 1, "location_summary": "Newport Beach, California", "locations": [ { "city": "Newport Beach", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01593891" }, { "nct_id": "NCT01602159", "title": "Revascularization With Open Bypass Versus Angioplasty and STenting of the Lower Extremity Trial (ROBUST)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Superficial Femoral Artery Stenosis", "Superficial Femoral Artery Occlusion", "Claudication", "Rest Pain" ], "interventions": [ { "name": "Open Bypass Surgery", "type": "PROCEDURE" }, { "name": "Angioplasty and Stenting", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Johns Hopkins University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 29, "start_date": "2009-07", "completion_date": "2014-06", "has_results": false, "last_update_posted_date": "2018-09-28", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 2, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" }, { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT01602159" }, { "nct_id": "NCT01205789", "title": "EXCEL Clinical Trial (Universal Registry)", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Chronic Coronary Occlusion", "Left Main Coronary Artery Disease", "Stent Thrombosis", "Vascular Disease", "Myocardial Ischemia", "Coronary Artery Stenosis", "Coronary Disease", "Coronary Artery Disease", "Coronary Restenosis" ], "interventions": [], "intervention_types": [], "sponsor": "Abbott Medical Devices", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1000, "start_date": "2010-10", "completion_date": "2012-09", "has_results": false, "last_update_posted_date": "2012-12-04", "last_synced_at": "2026-06-26T04:37:25.190Z", "location_count": 1, "location_summary": "Santa Clara, California", "locations": [ { "city": "Santa Clara", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT01205789" } ] }