A First in Human Study for the Versa Device for Tricuspid Regurgitation
NCT: NCT06368401 · ACTIVE_NOT_RECRUITING
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Brief 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.
Official Source
View on ClinicalTrials.gov →Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.
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