臨床試驗

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 2

NCT：NCT02777593 · ACTIVE_NOT_RECRUITING

NCT IDNCT02777593

狀態ACTIVE_NOT_RECRUITING

開始日期2016-09-06

SponsorW.L.Gore & Associates (INDUSTRY)

First posted2016-05-19

Last updated2026-09-10

簡要摘要

The objective of this study is to determine whether the GORE® TAG® Thoracic Branch Endoprosthesis is safe and effective in treating lesions of the aortic arch and descending thoracic aorta, requiring Zone 2 proximal implantation of the device.

官方來源

在 ClinicalTrials.gov 上查看 →

資料來自 ClinicalTrials.gov API。最新狀態請參閱官方紀錄。