{ "api_version": "1", "request": { "url": "https://clinicaltrialsfind.com/api/v1/search.json?intervention=Ultrasound+Guided+Approach&page=2", "query": { "intervention": "Ultrasound Guided Approach", "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=Ultrasound+Guided+Approach&page=1&page_size=10" }, "source": "remote", "last_synced_at": "2026-09-22T23:21:06.357Z", "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": "NCT03478735", "title": "Ultrasound Greater Occipital Nerve Block at C2 Level Compared to Landmark-based Greater Occipital Nerve Block", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Occipital Neuralgia", "Cervicogenic Headache", "Migraine Without Aura" ], "interventions": [ { "name": "Ultrasound Guided Greater Occipital Nerve Block at C2", "type": "PROCEDURE" }, { "name": "Landmark-Based Greater Occipital Nerve Block", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Mayo Clinic", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 32, "start_date": "2017-07-17", "completion_date": "2021-06-14", "has_results": false, "last_update_posted_date": "2021-06-15", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "Rochester, Minnesota", "locations": [ { "city": "Rochester", "state": "Minnesota" } ], "official_url": "https://clinicaltrials.gov/study/NCT03478735" }, { "nct_id": "NCT03231150", "title": "Plantar Fasciitis Randomized Clinical Control Trial", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Plantar Fascitis" ], "interventions": [ { "name": "Local Steroid Injection into the plantar heel", "type": "PROCEDURE" }, { "name": "Ultrasound Guided Injection", "type": "PROCEDURE" }, { "name": "Anatomical Guided injection", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of Pennsylvania", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 62, "start_date": "2017-03-28", "completion_date": "2026-10-31", "has_results": false, "last_update_posted_date": "2025-10-10", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT03231150" }, { "nct_id": "NCT07158892", "title": "Understanding Patient Preferences When Deciding on a Voluntary Musculoskeletal Test", "overall_status": "NOT_YET_RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Non-traumatic Musculoskeletal Conditions", "Carpal Tunnel Syndrome (CTS)", "Lateral Epicondylitis", "Osteoarthritis", "Trigger Digit", "Dupuytren Contracture", "Rotator Cuff Tendinopathy", "De Quervain Disease" ], "interventions": [ { "name": "Diagnostic Advance Care Planning Discussion", "type": "BEHAVIORAL" }, { "name": "Informational Statement Only", "type": "BEHAVIORAL" } ], "intervention_types": [ "BEHAVIORAL" ], "sponsor": "University of Texas at Austin", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 220, "start_date": "2026-10-25", "completion_date": "2027-03-01", "has_results": false, "last_update_posted_date": "2026-09-22", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "Austin, Texas", "locations": [ { "city": "Austin", "state": "Texas" } ], "official_url": "https://clinicaltrials.gov/study/NCT07158892" }, { "nct_id": "NCT07817147", "title": "CREO - Microwave Ablation Feasibility Study", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Pancreatic Cancer", "Liver Cancer (Locally Advanced or Metastatic)", "Pancreatic Cancer Non-resectable", "Pancreatic Cancer Stage III", "Pancreatic Cancer Stage IV", "Liver Cancer Stage IV", "Liver Cancer Stage IIIa", "Liver Cancer Stage IIIb", "Liver Cancer Stage IIIc" ], "interventions": [ { "name": "EUS-Guided MWA Device", "type": "DEVICE" } ], "intervention_types": [ "DEVICE" ], "sponsor": "Banner Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 75, "start_date": "2026-02-19", "completion_date": "2028-08", "has_results": false, "last_update_posted_date": "2026-09-14", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 7, "location_summary": "Gilbert, Arizona • Los Angeles, California • Chicago, Illinois + 4 more", "locations": [ { "city": "Gilbert", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Chicago", "state": "Illinois" }, { "city": "Rochester", "state": "Minnesota" }, { "city": "Knoxville", "state": "Tennessee" } ], "official_url": "https://clinicaltrials.gov/study/NCT07817147" }, { "nct_id": "NCT04661241", "title": "Mapping the Target for the MRgFUS Treatment of Tremor", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Tremor, Essential", "Parkinson's Disease" ], "interventions": [ { "name": "Automatic DRT/VIM target-recognition method using MR-SISET and ML approaches", "type": "OTHER" }, { "name": "Routine clinical MRI protocol", "type": "OTHER" } ], "intervention_types": [ "OTHER" ], "sponsor": "NYU Langone Health", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 6, "start_date": "2020-09-10", "completion_date": "2022-06-15", "has_results": false, "last_update_posted_date": "2022-08-15", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT04661241" }, { "nct_id": "NCT03946072", "title": "Transseptal vs Retrograde Aortic Ventricular Entry to Reduce Systemic Emboli", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Neurocognitive Dysfunction" ], "interventions": [ { "name": "Transseptal Aortic Approach Catheter Ablation Procedure", "type": "PROCEDURE" }, { "name": "Retrograde Aortic Approach Catheter Ablation Procedure", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "University of California, San Francisco", "sponsor_class": "OTHER", "healthy_volunteers": true, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 153, "start_date": "2019-07-02", "completion_date": "2023-11-25", "has_results": false, "last_update_posted_date": "2023-12-26", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 20, "location_summary": "Phoenix, Arizona • Los Angeles, California • Palo Alto, California + 14 more", "locations": [ { "city": "Phoenix", "state": "Arizona" }, { "city": "Los Angeles", "state": "California" }, { "city": "Los Angeles", "state": "California" }, { "city": "Palo Alto", "state": "California" }, { "city": "San Diego", "state": "California" } ], "official_url": "https://clinicaltrials.gov/study/NCT03946072" }, { "nct_id": "NCT04234347", "title": "Long Versus Short Axis Approach for Ultrasound Guided Peripheral Intravenous Access", "overall_status": "UNKNOWN", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Venous Access" ], "interventions": [ { "name": "Intravenous access method", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "Temple University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "99 Years", "sex": "ALL", "summary": "18 Years to 99 Years" }, "enrollment_count": 98, "start_date": "2024-05-01", "completion_date": "2025-12-01", "has_results": false, "last_update_posted_date": "2024-04-11", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "Philadelphia, Pennsylvania", "locations": [ { "city": "Philadelphia", "state": "Pennsylvania" } ], "official_url": "https://clinicaltrials.gov/study/NCT04234347" }, { "nct_id": "NCT07058155", "title": "Optimizing Portal Hypertension With TIPS and Interval Metabolic Surgery for Advanced Liver Disease", "overall_status": "RECRUITING", "study_type": "INTERVENTIONAL", "phases": [ "PHASE4" ], "conditions": [ "Liver Cirrhoses", "Portal Hypertension Related to Cirrhosis", "Severe Obesity", "TIPS" ], "interventions": [ { "name": "Transjugular Intrahepatic Portosystemic Shunt (TIPS)", "type": "PROCEDURE" }, { "name": "Sleeve Gastrectomy", "type": "PROCEDURE" }, { "name": "Anti-Obesity Pharmacotherapy (Class Effect)", "type": "DRUG" }, { "name": "Lifestyle Counseling - Diet & Physical-Activity Program", "type": "BEHAVIORAL" } ], "intervention_types": [ "PROCEDURE", "DRUG", "BEHAVIORAL" ], "sponsor": "The Cleveland Clinic", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": "70 Years", "sex": "ALL", "summary": "18 Years to 70 Years" }, "enrollment_count": 70, "start_date": "2025-12-17", "completion_date": "2034-02-01", "has_results": false, "last_update_posted_date": "2025-12-23", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "Cleveland, Ohio", "locations": [ { "city": "Cleveland", "state": "Ohio" } ], "official_url": "https://clinicaltrials.gov/study/NCT07058155" }, { "nct_id": "NCT01859559", "title": "Evaluate Initial Success Rate of Ultrasound Guided Versus Landmark Approach For Peripheral Intravenous Access", "overall_status": "COMPLETED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Patients With Peripheral Intravenous Access Lines" ], "interventions": [ { "name": "Ultrasound-guided peripheral intravenous access line placement", "type": "PROCEDURE" }, { "name": "Landmark Approach to peripheral intravenous access line placement", "type": "PROCEDURE" } ], "intervention_types": [ "PROCEDURE" ], "sponsor": "George Washington University", "sponsor_class": "OTHER", "healthy_volunteers": false, "eligibility": { "minimum_age": "18 Years", "maximum_age": null, "sex": "ALL", "summary": "18 Years and older" }, "enrollment_count": 1189, "start_date": "2013-08", "completion_date": "2014-09", "has_results": false, "last_update_posted_date": "2018-12-07", "last_synced_at": "2026-09-22T23:21:06.357Z", "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/NCT01859559" }, { "nct_id": "NCT03632655", "title": "A Prospective, Randomized Trial Comparing Office-based MR-guided Prostate Biopsy Approaches", "overall_status": "TERMINATED", "study_type": "INTERVENTIONAL", "phases": [ "NA" ], "conditions": [ "Prostate Cancer", "Elevated PSA" ], "interventions": [ { "name": "prostate biopsy", "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": "MALE", "summary": "18 Years and older · Male only" }, "enrollment_count": 38, "start_date": "2017-12-23", "completion_date": "2020-10-08", "has_results": true, "last_update_posted_date": "2024-05-31", "last_synced_at": "2026-09-22T23:21:06.357Z", "location_count": 1, "location_summary": "New York, New York", "locations": [ { "city": "New York", "state": "New York" } ], "official_url": "https://clinicaltrials.gov/study/NCT03632655" } ] }