GORE VIABAHN Endoprosthesis Post-Marketing Surveillance Study

  • STATUS
    Recruiting
  • participants needed
    100
  • sponsor
    W.L.Gore & Associates
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Updated on 19 February 2024
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Summary

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.

Details
Condition Vascular Stent-Graft Stenosis
Age 100years or below
Treatment GORE® VIABAHN® Stent Graft
Clinical Study IdentifierNCT04429243
SponsorW.L.Gore & Associates
Last Modified on19 February 2024

Eligibility

 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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Additional screening procedures may be conducted by the study team before you can be confirmed eligible to participate.

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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