Clinical Trial

Improved Outcomes With Pre-Procedure Shockwave IVL of Common Femoral Artery Access Site Prior to Large Bore Access and Pre-Closure

Recruiting
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Summary
The primary purpose of this study is to observe reduced access site complications in patients with heavily calcified common femoral arteries requiring Transcatheter Aortic Valve Replacement (TAVR)
Trial Details
NCT Number NCT07205068
Lead Sponsor University of Tennessee Graduate School of Medicine
Collaborators: Shockwave Medical, Inc.
Conditions Aortic Stenosis
Enrollment 100 participants
Start Date 2025-10-04
Primary Completion 2026-11-04 (estimated)
Study Completion 2026-11-04 (estimated)
Updated on ClinicalTrials.gov 2025-10-03