A First in Human Study for the Versa Device for Tricuspid Regurgitation

Status Not yet recruiting

Clinical Trial Summary

This study is prospective, non-randomized, single-arm,first in human study to evaluate the safety and feasibility of the Versa Vascular System for intervention in adults with severe tricuspid regurgitation who are not surgical candidates.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06368401
Study type	Interventional
Source	Versa Vascular, Inc
Contact	Aaron Grogan
Phone	650 265 8123
Email	aaron@versavascular.com
Status	Not yet recruiting
Phase	N/A
Start date	June 1, 2024
Completion date	December 31, 2025

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See also
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