Abstract

The Zilver Vena Venous Stent (Cook Medical, Limerick, Ireland) was evaluated under the VIVO Clinical Study (NCT01970007), a prospective, global, single-arm, investigational study, designed to evaluate the safety and effectiveness for the treatment of symptomatic iliofemoral venous outflow obstruction. An understanding of longer-term treatment outcomes is vital; therefore, the purpose of this study update is to report on 3-year patency, clinical improvement, and stent integrity by patient subgroup.

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