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Clinical Trial

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1

NCT: NCT02777528 · ACTIVE_NOT_RECRUITING

NCT IDNCT02777528
StatusACTIVE_NOT_RECRUITING
Start Date2016-08
Completion2028-03
SponsorW.L.Gore & Associates (INDUSTRY)
First posted
Last updated

Brief Summary

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.

Frequently Asked Questions

What is Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1?

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1 is a clinical trial registered under NCT02777528. Current status: ACTIVE_NOT_RECRUITING.

What is the status of NCT02777528?

The current status of NCT02777528 (Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1) is: ACTIVE_NOT_RECRUITING.

When did Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1 start?

Evaluation of the GORE® TBE Device in the Treatment of Lesions of the Aortic Arch and Descending Thoracic Aorta, Zone 0/1 started on 2016-08.

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Official Source

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Data sourced from ClinicalTrials.gov API. For the most current status, refer to the official record.