{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Obstruction&page=36", "query": { "condition": "Obstruction", "page": 36 }, "page_size": 10 }, "pagination": { "page": 36, "page_size": 10, "total_count": 2396, "total_pages": 240, "next_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Obstruction&page=37&page_size=10", "previous_page_url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Obstruction&page=35&page_size=10" }, "source": "remote", "last_synced_at": "2026-10-28T16:01:35.419Z", "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": "NCT05541679", "title": "Comparison of Left Bundle Branch Area Versus Right Ventricular Septal Pacing in Patients With High-degree Conduction Disease After Transcatheter Aortic Valve Replacement (Left Bundle BRAVE)", "overall_status": "ACTIVE_NOT_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Complete Heart Block", "High Degree Second Degree Atrioventricular Block", "Pacemaker-Induced Cardiomyopathy", "Aortic Valve Stenosis" ], "interventions": [ { "name": "Right ventricular septal pacing followed by left bundle branch area pacing", "type": "DEVICE" }, { "name": "Left bundle branch area pacing followed by right ventricular septal pacing", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Main Line Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 46, "start_date": "2022-12-28", "completion_date": "2025-12-31", "has_results": false, "last_update_posted_date": "2024-12-10", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 4, "location_summary": "Overland Park, Kansas • Ridgewood, New Jersey • Philadelphia, Pennsylvania + 1 more", "locations": [ { "city": "Overland Park", "state": "Kansas" }, { "city": "Ridgewood", "state": "New Jersey" }, { "city": "Philadelphia", "state": "Pennsylvania" }, { "city": "Wynnewood", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT05541679" }, { "nct_id": "NCT05265520", "title": "His-Bundle Corrective Pacing in Heart Failure", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Right Bundle-Branch Block", "Heart Failure", "His-bundle Pacing", "Cardiac Resynchronization Therapy" ], "interventions": [ { "name": "His-CRT implantation", "type": "PROCEDURE" }, { "name": "BIV-CRT implantation", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Rochester", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 120, "start_date": "2022-12-02", "completion_date": "2028-07-01", "has_results": false, "last_update_posted_date": "2026-02-09", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 14, "location_summary": "Phoenix, Arizona • Los Angeles, California • Tampa, Florida + 8 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Tampa", "state": "Florida" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05265520" }, { "nct_id": "NCT05640115", "title": "Obstruction of Malignancy: Percutaneous Renal vs Endoscopic Stent", "overall_status": "WITHDRAWN", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Cancer", "Urinary Obstruction", "Malignancy", "Urinary Dysfunction", "Ureter Obstruction", "Ureter Injury" ], "interventions": [ { "name": "Ureteral Stent", "type": "DEVICE" }, { "name": "Percutaneous Nephrostomy Tube Placement", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "University of Chicago", "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": "2023-09-22", "completion_date": "2024-08-21", "has_results": false, "last_update_posted_date": "2024-12-19", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "Chicago, Illinois", "locations": [ { "city": "Chicago", "state": "Illinois" } ], "official_url": "https://clinicaltrials.gov/study/NCT05640115" }, { "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": "2026-10-28T16:01:35.419Z", "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": "NCT05521789", "title": "Erector Spinae Block for Thoracic Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Pulmonary Neoplasm", "Pulmonary Cancer", "Thoracic Diseases", "Thoracic Cancer", "Thoracic Neoplasms" ], "interventions": [ { "name": "ESB Thoracic", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "90 Years", "sex": "ALL", "summary": "18 Years to 90 Years" }, "enrollment_count": 70, "start_date": "2022-07-22", "completion_date": "2027-07-21", "has_results": false, "last_update_posted_date": "2026-02-25", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "Washington D.C., District of Columbia", "locations": [ { "city": "Washington D.C.", "state": "District of Columbia" } ], "official_url": "https://clinicaltrials.gov/study/NCT05521789" }, { "nct_id": "NCT05481814", "title": "CPX in Paradoxical Low Flow Aortic Stenosis", "overall_status": "WITHDRAWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Aortic Valve Stenosis" ], "interventions": [], "intervention_types": [], "sponsor": "Henry Ford Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 0, "start_date": "2017-09-30", "completion_date": "2022-07-01", "has_results": false, "last_update_posted_date": "2022-08-01", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "Detroit, Michigan", "locations": [ { "city": "Detroit", "state": "Michigan" } ], "official_url": "https://clinicaltrials.gov/study/NCT05481814" }, { "nct_id": "NCT03487549", "title": "Cantharidin and Occlusion in Verruca Epithelium", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE2" ], "conditions": [ "Common Wart", "Warts Hand", "Warts", "Papillomavirus Infections", "DNA Virus Infections", "Skin Diseases, Viral", "Skin Diseases, Infectious", "Skin Diseases", "Virus Diseases", "Tumor Virus Infections", "Verruca Vulgaris", "Verruca" ], "interventions": [ { "name": "VP-102 Cantharidin, topical film forming solution", "type": "COMBINATION_PRODUCT" } ], "intervention_types": [ "COMBINATION_PRODUCT" ], "sponsor": "Verrica Pharmaceuticals Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "2 Years", "maximum_age": null, "sex": "ALL", "summary": "2 Years and older" }, "enrollment_count": 56, "start_date": "2018-03-27", "completion_date": "2019-07-15", "has_results": true, "last_update_posted_date": "2024-11-27", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 5, "location_summary": "Little Rock, Arkansas • Jacksonville, Florida • Plainfield, Indiana + 2 more", "locations": [ { "city": "Little Rock", "state": "Arkansas" }, { "city": "Jacksonville", "state": "Florida" }, { "city": "Plainfield", "state": "Indiana" }, { "city": "Clarkston", "state": "Michigan" }, { "city": "Raleigh", "state": "North Carolina" } ], "official_url": "https://clinicaltrials.gov/study/NCT03487549" }, { "nct_id": "NCT06731998", "title": "Optimal Perioperative Pain Control in Minimally Invasive Abdominal Cancer Surgery", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Oncologic Surgery", "Cancer", "Cancer Surgery", "Hepatic Cancer", "Gastric (Cardia, Body) Cancer", "Biliary Tract Cancer", "Pancreatic Cancer Resectable", "Gynecologic Cancers", "Gastrointestinal Cancers", "Colorectal Cancer", "Minimally Invasive Surgical Procedures" ], "interventions": [ { "name": "Local Anesthesia", "type": "PROCEDURE" }, { "name": "Laparoscopic Transversus Abdominis Plane block", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Allegheny Singer Research Institute (also known as Allegheny Health Network Research Institute)", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "89 Years", "sex": "ALL", "summary": "18 Years to 89 Years" }, "enrollment_count": 48, "start_date": "2025-02-05", "completion_date": "2026-12", "has_results": false, "last_update_posted_date": "2025-09-18", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT06731998" }, { "nct_id": "NCT00645138", "title": "Comparison of Paravertebral Block With General Anesthesia in Patients Undergoing Breast Cancer Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "PHASE3" ], "conditions": [ "Breast Cancer" ], "interventions": [ { "name": "Paravertebral Block", "type": "PROCEDURE" }, { "name": "General Anesthesia", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Weill Medical College of Cornell University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "FEMALE", "summary": "18 Years and older · Female only" }, "enrollment_count": 40, "start_date": "2008-04", "completion_date": "2010-03", "has_results": false, "last_update_posted_date": "2011-08-05", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT00645138" }, { "nct_id": "NCT02849678", "title": "A Pain Study Comparing Two Commonly Used Medications to Treat Pain After Bowel Surgery", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Postoperative Pain" ], "interventions": [ { "name": "Ropivacaine", "type": "DRUG" }, { "name": "Lidocaine", "type": "DRUG" } ], "intervention_types": [ "DRUG" ], "sponsor": "Jacques E. Chelly", "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": 68, "start_date": "2008-01", "completion_date": "2016-05", "has_results": true, "last_update_posted_date": "2018-03-20", "last_synced_at": "2026-10-28T16:01:35.419Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT02849678" } ] }