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GORE VIABAHN Endoprosthesis Post-Marketing Surveillance Study

GORE VIABAHN Endoprosthesis Post-Marketing Surveillance Study

Recruiting
100 years and younger
All
Phase N/A

Overview

This study will confirm the efficacy and safety in the clinical setting after the launch of the GORE VIABAHN stent graft (hereafter referred to as "Viabahn") for the treatment of patients with stenosis or occlusion at the venous anastomosis of synthetic arteriovenous access graft.

Eligibility

Inclusion Criteria:

  • Participants who developed stenosis or occlusion at the venous anastomosis of synthetic arteriovenous access graft
  • Participants who was used to repair vascular access circuits for purposes other than treatment of stenosis or occlusion at the venous anastomosis of synthetic arteriovenous access graft

Study details
    Vascular Stent-Graft Stenosis

NCT04429243

W.L.Gore & Associates

5 August 2020

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