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ABSTRACT: Purpose
To assess safety and patency of the Venovo venous stent for the treatment of iliofemoral vein obstruction.Materials and methods
Twenty-two international centers enrolled 170 patients in the VERNACULAR study (93 post-thrombotic syndrome; 77 non-thrombotic iliac vein lesions). Primary outcome measures were major adverse events at 30 days and 12-month primary patency (freedom from target vessel revascularization, thrombotic occlusion, or stenosis > 50%). Secondary outcomes included the Venous Clinical Severity Score Pain Assessment and Chronic Venous Quality-of-Life Questionnaire assessments (hypothesis tested). Secondary observations included primary patency, target vessel and lesion revascularization (TVR/TLR), and assessment of stent integrity through 36 months.
SUBMITTER: Dake MD
PROVIDER: S-EPMC8451739 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature