{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Standard+Balloon+Angioplasty&page=2", "query": { "intervention": "Standard Balloon 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?intervention=Standard+Balloon+Angioplasty&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-28T22:01:13.310Z", "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": "NCT02063672", "title": "Lutonix® Drug Coated Balloon vs. Standard Balloon Angioplasty for Treatment of Femoropopliteal In-Stent Restenosis", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Femoral Artery Stenosis", "Femoral Artery Occlusion", "Restenosis" ], "interventions": [ { "name": "Lutonix DCB", "type": "DEVICE" }, { "name": "Standard Uncoated Balloon Angioplasty Catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "C. R. Bard", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 82, "start_date": "2014-03", "completion_date": "2019-03", "has_results": true, "last_update_posted_date": "2019-04-11", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 20, "location_summary": "Fairhope, Alabama • New Haven, Connecticut • Washington D.C., District of Columbia + 17 more", "locations": [ { "city": "Fairhope", "state": "Alabama" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Lakeland", "state": "Florida" }, { "city": "Miami", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT02063672" }, { "nct_id": "NCT00178672", "title": "A Single Center of Carotid Stenting With Distal Protection for the Treatment of Obstructive Carotid Artery Disease", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Heart Disease", "Brain Vascular Accident", "Carotid Artery Disease", "Carotid Stenosis" ], "interventions": [ { "name": "Angioguard XP distal protection device", "type": "DEVICE" }, { "name": "Heart Catheterization -Angioplasty", "type": "PROCEDURE" }, { "name": "stenting", "type": "DEVICE" } ], "intervention_types": [ "DEVICE", "PROCEDURE" ], "sponsor": "The University of Texas Health Science Center, Houston", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 69, "start_date": "2002-11", "completion_date": "2007-08", "has_results": false, "last_update_posted_date": "2020-11-05", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00178672" }, { "nct_id": "NCT00687076", "title": "Effectiveness of Intensive Lipid Modification Medication in Preventing the Progression of Peripheral Arterial Disease (The ELIMIT Study)", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Peripheral Arterial Disease" ], "interventions": [ { "name": "Ezetimibe", "type": "DRUG" }, { "name": "Niaspan", "type": "DRUG" }, { "name": "Statin therapy", "type": "DRUG" }, { "name": "Standard care", "type": "BEHAVIORAL" }, { "name": "Aspirin", "type": "DRUG" }, { "name": "Clopidogrel", "type": "DRUG" }, { "name": "Placebo Niaspan", "type": "DRUG" }, { "name": "Placebo Ezetimibe", "type": "DRUG" }, { "name": "Percutaneous transluminal angioplasty (PTA)", "type": "PROCEDURE" } ], "intervention_types": [ "DRUG", "BEHAVIORAL", "PROCEDURE" ], "sponsor": "Baylor College of Medicine", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "40 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "40 Years to 80 Years" }, "enrollment_count": 102, "start_date": "2004-04", "completion_date": "2010-12", "has_results": true, "last_update_posted_date": "2020-02-06", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00687076" }, { "nct_id": "NCT01268319", "title": "CANARY: Coronary Assessment by Near-infrared of Atherosclerotic Rupture-prone Yellow", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Coronary Atherosclerosis", "Myocardial Infarction", "Coronary Plaque Embolization" ], "interventions": [ { "name": "Embolic Protection Device (EPD)", "type": "DEVICE" }, { "name": "Intracoronary Spectroscopy and Ultrasonic Evaluation", "type": "DEVICE" }, { "name": "Angioplasty and Stent Implant", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Infraredx", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 85, "start_date": "2011-05", "completion_date": "2016-11", "has_results": false, "last_update_posted_date": "2017-06-12", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 9, "location_summary": "Scottsdale, Arizona • San Francisco, California • Washington D.C., District of Columbia + 6 more", "locations": [ { "city": "Scottsdale", "state": "Arizona" }, { "city": "San Francisco", "state": "California" }, { "city": "Washington D.C.", "state": "District of Columbia" }, { "city": "Grand Rapids", "state": "Michigan" }, { "city": "Royal Oak", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT01268319" }, { "nct_id": "NCT03175744", "title": "Stellarex DCB Versus Standard Balloon Angioplasty for Treatment of Below-The-Knee (BTK) Arteries", "overall_status": "SUSPENDED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Critical Limb Ischemia" ], "interventions": [ { "name": "Stellarex DCB", "type": "DEVICE" }, { "name": "PTA Catheter", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Spectranetics Corporation", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "85 Years", "sex": "ALL", "summary": "18 Years to 85 Years" }, "enrollment_count": 82, "start_date": "2017-05-24", "completion_date": "2025-10", "has_results": false, "last_update_posted_date": "2023-06-22", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 9, "location_summary": "Orange, California • Bradenton, Florida • Houma, Louisiana + 6 more", "locations": [ { "city": "Orange", "state": "California" }, { "city": "Bradenton", "state": "Florida" }, { "city": "Houma", "state": "Louisiana" }, { "city": "Hackensack", "state": "New Jersey" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03175744" }, { "nct_id": "NCT05616104", "title": "FLEX FIRST Registry Research Protocol", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Arteriovenous Fistula", "Arteriovenous Graft", "Fistula", "Arterial Occlusive Diseases" ], "interventions": [ { "name": "FLEX Vessel Prep System", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "VentureMed Group Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 130, "start_date": "2022-11-29", "completion_date": "2025-08-04", "has_results": false, "last_update_posted_date": "2025-08-07", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 4, "location_summary": "Miami, Florida • New Brighton, Minnesota • Orangeburg, South Carolina + 1 more", "locations": [ { "city": "Miami", "state": "Florida" }, { "city": "New Brighton", "state": "Minnesota" }, { "city": "Orangeburg", "state": "South Carolina" }, { "city": "Spartanburg", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT05616104" }, { "nct_id": "NCT03566927", "title": "FLEX®-DCB Dialysis ACCESS Stenosis Study", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Arteriovenous Fistula" ], "interventions": [ { "name": "FLEX Scoring Catheter with Lutonix DCB", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "VentureMed Group Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "21 Years", "maximum_age": null, "sex": "ALL", "summary": "21 Years and older" }, "enrollment_count": 34, "start_date": "2018-05-29", "completion_date": "2019-12-10", "has_results": false, "last_update_posted_date": "2021-02-17", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 1, "location_summary": "Orangeburg, South Carolina", "locations": [ { "city": "Orangeburg", "state": "South Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03566927" }, { "nct_id": "NCT06330493", "title": "AcoArt Litos PCB Below-the-knee Global Trial", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Chronic Limb-Threatening Ischemia" ], "interventions": [ { "name": "PCB", "type": "DEVICE" }, { "name": "PTA", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Acotec Scientific Co., Ltd", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2025-10-10", "completion_date": "2026-08-24", "has_results": false, "last_update_posted_date": "2026-08-26", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 16, "location_summary": "Concord, California • Fremont, California • New Haven, Connecticut + 12 more", "locations": [ { "city": "Concord", "state": "California" }, { "city": "Fremont", "state": "California" }, { "city": "New Haven", "state": "Connecticut" }, { "city": "Hialeah", "state": "Florida" }, { "city": "Jacksonville", "state": "Florida" } ], "official_url": "https://clinicaltrials.gov/study/NCT06330493" }, { "nct_id": "NCT06434194", "title": "Serrantor OCT Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Critical Limb Ischemia" ], "interventions": [ { "name": "Serranator PTA Serration Catheter", "type": "DEVICE" }, { "name": "PTA (Standard of Care)", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Cagent Vascular LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "19 Years", "maximum_age": null, "sex": "ALL", "summary": "19 Years and older" }, "enrollment_count": 60, "start_date": "2024-10-31", "completion_date": "2025-06-01", "has_results": false, "last_update_posted_date": "2025-05-18", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 2, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" }, { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06434194" }, { "nct_id": "NCT02237066", "title": "Understanding Angioplasty by the Chocolate PTA Balloon Catheter Compared to Conventional PTA Balloons Via OCT Imaging", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Infrainguinal Peripheral Arterial Disease" ], "interventions": [ { "name": "Chocolate PTA Balloon Angioplasty", "type": "DEVICE" }, { "name": "Standard PTA Balloon Angioplasty", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "TriReme Medical, LLC", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 0, "start_date": "2014-09", "completion_date": "2015-03", "has_results": false, "last_update_posted_date": "2015-03-19", "last_synced_at": "2026-09-28T22:01:13.310Z", "location_count": 2, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" }, { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT02237066" } ] }