At a glance
ClinicalIndex Comparison RecordN/ACompleted· 243 enrolled
Drug / intervention
Zilver Vena Venous Self-Expanding Stentdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Evaluation of the Zilver® Vena™ Venous Stent in the Treatment of Symptomatic Iliofemoral Venous Outflow Obstruction
In Brief
A clinical study evaluating Zilver Vena Venous Self-Expanding Stent for Symptomatic Venous Outflow Obstruction in the Iliofemoral Vein. Completed, enrolled 243 participants across 30 sites in 2 countries.
Detailed Summary
The purpose of the VIVO Clinical Study is to evaluate the safety and effectiveness of the Zilver® Vena™ Venous Stent in the treatment of symptomatic iliofemoral venous outflow obstruction.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesTaiwan, United States
Collaborators--
Timeline
N/ACompletedFinished
2014201520162017201820192020202120222023202420252026
First PostedOct 2013
Enrollment StartDec 2013
Primary CompletionNov 2017
Study CompletionNov 2019
TodayJul 2026
First PostedOct 25, 2013
Enrollment StartDec 13, 2013
Primary CompletionNov 20, 2017
Study CompletionNov 20, 2019
TodayJul 2, 2026
Enrollment to primary: 3.9 yearsPosted 12.7 years ago
Interventions
Zilver Vena Venous Self-Expanding Stentdevice
stenting