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Clinical Trial Summary

This is a prospective, multi-center, single-arm, non-blinded clinical trial designed to investigate the safety and efficacy of the Vesper DUO Venous Stent System as compared to a pre-defined performance goal (PG) established from published, peer reviewed scientific literature related to stenting of iliofemoral venous outflow obstructions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04580160
Study type Interventional
Source Vesper Medical, Inc.
Contact
Status Active, not recruiting
Phase N/A
Start date November 30, 2020
Completion date December 2024

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