Evaluation of the Zilver® Vena™ Venous Stent

NCT01663051 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 35

Last updated 2016-11-01

No results posted yet for this study

Summary

This prospective, non-randomized, multi-center study is intended to evaluate the Zilver® Vena™ stent in the treatment of symptomatic iliofemoral venous outflow obstruction.

Conditions

  • Iliofemoral Venous Outflow Obstruction

Interventions

DEVICE

Zilver Vena Venous Stent

Stenting iliofemoral venous outflow obstruction

Sponsors & Collaborators

  • Cook Group Incorporated

    lead INDUSTRY

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-11-30
Primary Completion
2016-07-31
Completion
2016-07-31

Countries

  • Germany
  • Ireland
  • Spain
  • Switzerland
  • United Kingdom

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01663051 on ClinicalTrials.gov