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

Active, not recruiting · Not applicable · NCT02777593

Conditions: Aortic Aneurysm, Thoracic, Aorta, Lesion

At a glance

Research payments reported, 2025
$49,366
U.S. investigators named
14
Sites paid
20
Planned or actual enrollment
250

About the trial

Sponsor
W.L.Gore & Associates
Tested
GORE® TAG® Thoracic Branch Endoprosthesis (device)
Dates
Started 2016-09-06; completion 2027-12
Results posted
Yes

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.

From ClinicalTrials.gov, last updated 2026-09-10. Full record, eligibility and contacts (opens in a new tab)

Industry funding

W. L. Gore & Associates, Inc. reported $49,366 in research payments for this study in 2025 (30 payments).

Products named: Product in Development, Gore Tag Thoracic Branch Endoprosthesis

Research payments usually go to hospitals, universities and research sites to run a study, not to the investigators personally. A payment is not evidence of wrongdoing.

U.S. investigators named on this study

Clinicians the company named as principal investigators in its Open Payments reports.

Sites paid to run it

Sources: CMS Open Payments research payments (program year 2025) and ClinicalTrials.gov, U.S. National Library of Medicine.