{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?condition=Ultrasonography%2C+Interventional&page=2", "query": { "condition": "Ultrasonography, Interventional", "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=Ultrasonography%2C+Interventional&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-27T11:06:53.617Z", "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": "NCT00102544", "title": "Use of Tracking Devices to Locate Abnormalities During Invasive Procedures", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Adenocarcinoma", "Prostate Neoplasms", "Prostate Cancer", "Renal Cell Carcinoma", "Von Hippel Lindau Disease" ], "interventions": [ { "name": "EM Tracking", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "National Institutes of Health Clinical Center (CC)", "sponsor_class": "NIH", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "120 Years", "sex": "ALL", "summary": "18 Years to 120 Years" }, "enrollment_count": 3894, "start_date": "2005-02-23", "completion_date": "2028-08-02", "has_results": false, "last_update_posted_date": "2026-07-24", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Bethesda, Maryland", "locations": [ { "city": "Bethesda", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT00102544" }, { "nct_id": "NCT07209527", "title": "Truway Diagnostic Tools in Primary Care", "overall_status": "ENROLLING_BY_INVITATION", "study_type": "INTERVENTIONAL", "phases": [ "EARLY_PHASE1" ], "conditions": [ "Chronic Disease", "Type 2 Diabetes Mellitus (T2DM), Obesity, Overweight", "Hypertension", "Cardiovascular Disease Acute", "Hyperlipidemia", "Chronic Kidney Disease (CKD), Stages 3-4 Exercise Tolerance / Functional Capacity Vascular Health / Arterial Stiffness Fatigue in CKD", "Peripheral Artery Disease", "Metabolic Syndrome", "Prediabetes" ], "interventions": [ { "name": "Truway Portable Ultrasound Device", "type": "DEVICE" }, { "name": "Truway Blood Glucose Monitor", "type": "DEVICE" }, { "name": "Standard Oral Hypoglycemic Agent", "type": "DRUG" } ], "intervention_types": [ "DEVICE", "DRUG" ], "sponsor": "Truway Health, Inc.", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": null, "maximum_age": null, "sex": "ALL", "summary": "Not listed" }, "enrollment_count": 200, "start_date": "2025-10-01", "completion_date": "2028-10-01", "has_results": false, "last_update_posted_date": "2025-10-24", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT07209527" }, { "nct_id": "NCT03226535", "title": "Ultrasound-CT Fusion System for Interventional Radiology Procedures", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "CT Guided Biopsy", "CT Guided Drain Placement Within the Abdomen or Pelvis", "CT Guided Injection of Muscle or Nerve Within the Pelvis" ], "interventions": [ { "name": "Ultrasound-CT Fusion", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Clear Guide Medical", "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": 20, "start_date": "2017-06-22", "completion_date": "2018-06-22", "has_results": false, "last_update_posted_date": "2017-07-21", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT03226535" }, { "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": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Houston, Texas", "locations": [ { "city": "Houston", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT00687076" }, { "nct_id": "NCT03504111", "title": "PRINT Trial (Platelet Rich Injection vs Needle Tenotomy)", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Lateral Epicondylitis", "Tendinosis", "Elbow, Tennis", "Elbows Tendonitis" ], "interventions": [ { "name": "Percutaneous Needle Tenotomy", "type": "PROCEDURE" }, { "name": "PRP", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Kaiser Permanente", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 50, "start_date": "2016-07", "completion_date": "2019-12-31", "has_results": false, "last_update_posted_date": "2019-03-13", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Los Angeles, California", "locations": [ { "city": "Los Angeles", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03504111" }, { "nct_id": "NCT01438385", "title": "Interventional Endoscopy Database for Pancreatico-biliary, Gastrointestinal and Esophageal Disorders", "overall_status": "UNKNOWN", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Ampullary Cancer", "Duodenal Cancer", "Bile Duct Cancer", "Bile Duct Disorders", "Gallstones", "Obstructive Jaundice", "Pancreatic Disorders (Noncancerous)", "Colorectal Cancer", "Esophageal Cancer", "Barrett's Esophagus", "Gastric Malignancies", "Pancreatic Cancer", "Pediatric Gastroenterology", "Cholangiocarcinoma", "Pancreatic Pseudocysts", "Acute and Chronic Pancreatitis", "Recurrent Pancreatitis", "Cholangitis", "Bile Leak", "Biliary Strictures", "Pancreatic Divisum", "Biliary and Pancreatic Stones", "Choledocholithiasis" ], "interventions": [ { "name": "Interventional Endoscopy", "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": "ALL", "summary": "18 Years and older" }, "enrollment_count": 12000, "start_date": "2011-07", "completion_date": "2017-12-30", "has_results": false, "last_update_posted_date": "2017-02-20", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT01438385" }, { "nct_id": "NCT06579989", "title": "Usefulness and Feasibility of Ultrasound in Office Laryngology Procedures", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Cough", "Vocal Cord Atrophy", "Vocal Cord Paresis", "Vocal Cord Paralysis", "Dysphagia", "Dysphonia" ], "interventions": [ { "name": "Ultrasound for cough", "type": "DIAGNOSTIC_TEST" }, { "name": "Ultrasound for vocal fold atrophy or vocal fold paresis/paralysis", "type": "DIAGNOSTIC_TEST" }, { "name": "Ultrasound for dysphagia", "type": "DIAGNOSTIC_TEST" }, { "name": "Ultrasound for dysphonia", "type": "DIAGNOSTIC_TEST" } ], "intervention_types": [ "DIAGNOSTIC_TEST" ], "sponsor": "Weill Medical College of Cornell University", "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": 200, "start_date": "2027-01", "completion_date": "2030-01", "has_results": false, "last_update_posted_date": "2026-06-16", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT06579989" }, { "nct_id": "NCT01612026", "title": "Ultrasound Versus Fluoroscopically-guided Arterial Access in Non-cardiac Vascular Patients", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Arterial Cannulation During Vascular Procedures" ], "interventions": [ { "name": "arterial cannulation by angiographic imaging", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "CAMC Health System", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": "80 Years", "sex": "ALL", "summary": "18 Years to 80 Years" }, "enrollment_count": 643, "start_date": "2013-03", "completion_date": "2017-10", "has_results": false, "last_update_posted_date": "2026-08-18", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Charleston, West Virginia", "locations": [ { "city": "Charleston", "state": "West Virginia" } ], "official_url": "https://clinicaltrials.gov/study/NCT01612026" }, { "nct_id": "NCT00330590", "title": "Central Venous Access Catheter Placement Using the Sonic Flashlight", "overall_status": "COMPLETED", "study_type": "OBSERVATIONAL", "phases": [], "conditions": [ "Catheterization, Central Venous" ], "interventions": [], "intervention_types": [], "sponsor": "University of Pittsburgh", "sponsor_class": "OTHER", "healthy_volunteers": null, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 150, "start_date": null, "completion_date": "2006-12", "has_results": false, "last_update_posted_date": "2008-02-15", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Pittsburgh, Pennsylvania", "locations": [ { "city": "Pittsburgh", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT00330590" }, { "nct_id": "NCT06095804", "title": "Clinical Pilot Study of the Percutaneous Ultrasound Jejunostomy Procedure", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Jejunostomy; Complications", "Enteral and Supplement Feeds Adverse Reaction", "Safety Issues" ], "interventions": [ { "name": "Percutaneous Ultrasound Jejunostomy", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "CoapTech", "sponsor_class": "INDUSTRY", "healthy_volunteers": false, "eligibility": { "minimum_age": "22 Years", "maximum_age": null, "sex": "ALL", "summary": "22 Years and older" }, "enrollment_count": 10, "start_date": "2023-12-01", "completion_date": "2025-07-01", "has_results": false, "last_update_posted_date": "2023-10-23", "last_synced_at": "2026-09-27T11:06:53.617Z", "location_count": 1, "location_summary": "Baltimore, Maryland", "locations": [ { "city": "Baltimore", "state": "Maryland" } ], "official_url": "https://clinicaltrials.gov/study/NCT06095804" } ] }