GORE VIABAHN Endoprosthesis Post-Marketing Surveillance Study

  • End date
    Jul 6, 2023
  • participants needed
  • sponsor
    W.L.Gore & Associates
Updated on 26 January 2021


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.

Condition Vascular Stent-Graft Stenosis, Vascular Stent-Graft Stenosis, Vascular Stent-Graft Stenosis
Treatment GORE® VIABAHN® Stent Graft
Clinical Study IdentifierNCT04429243
SponsorW.L.Gore & Associates
Last Modified on26 January 2021


Yes No Not Sure

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
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