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Aortic Arch DissectionDevice

What this study is

A prospective multi-center post-market study collecting outcomes through at least 5-years and up to 10-years post procedure for subjects treated with the TBE Device in Zone 0/1 as part of routine clinical practice.

What's being tested

  • GORE® TAG® Thoracic Branch Endoprosthesis

    Intervention · DEVICE

    Lesions in aortic arch in Zone 0 or Zone 1

Study details

Sponsor
W.L.Gore & Associates
Conditions
Aortic Arch Dissection · Aortic Arch Aneurysm
Enrolling
125 people
Starts
2026-03-02
Est. completion
2036-03
Design
Open-label, single group
Record
View on ClinicalTrials.gov ↗