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Evaluation of the Sinus-Venous Stent for the Treatment of Iliofemoral Venous Occlusive Disease

NCT02799914 · Status: WITHDRAWN · Type: OBSERVATIONAL

Last updated 2019-02-08

No results posted yet for this study

Summary

Post market clinical follow-up study about the Sinus-venous stent. Patients with venous iliofemoral occlusive disease are treated with the Sinus-venous stent. This observational study will provide 1 year data about safety and efficacy.

Conditions

  • Venous Vascular Diseases and Syndromes

Interventions

DEVICE

Sinus-Venous stent (Optimed GmbH)

Stent implantation

Sponsors & Collaborators

  • Archer Research

    collaborator INDUSTRY

  • be Medical

    lead INDUSTRY

Principal Investigators

  • Geert Lauwers, MD · Ziekenhuis Oost-Limburg

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2018-06-30
Completion
2018-06-30

Countries

  • Belgium

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 NCT02799914 on ClinicalTrials.gov