Ensayo clínico

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

ID NCTNCT02777593

EstadoACTIVE_NOT_RECRUITING

Fecha de inicio2016-09-06

SponsorW.L.Gore & Associates (INDUSTRY)

First posted2016-05-19

Last updated2026-09-10

Resumen breve

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.

Fuente oficial

Ver en ClinicalTrials.gov →

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