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Gore TBE PAS (25-03) - Clinical Trial

¿Cuál es el Propósito de este estudio?

In this study, people will be treated with the Gore TBE device as part of their regular surgery planned by their doctor. The study will collect information from normal follow up visits for up to ten years. Participants will also be asked to fill out a questionnaire before surgery and again at each follow up visit to help doctors understand how they are doing over time.

¿Cuál es la Condición que se está estudiando?

Thoracic aortic conditions

¿Quién puede participar en el Estudio?

This study is for adults who have a problem with the main blood vessel in the chest, called the thoracic aorta. These adults are planning to be treated with a medical device called the Gore TBE device as part of their care.

Grupo etario
Adultos

¿Qué Implica?

The purpose of this study is to collect information about how well a medical device called the Gore TAG Thoracic Branch Endoprosthesis works. Doctors will also look at how patients do over a long period of time after receiving the device. This information will help doctors understand the safety and long term results of using this device.

Detalles del Estudio

Título Completo
GORE TAG Thoracic Branch Endoprosthesis Zone 0/1 Post-Approval Study
Investigador Principal
G. Chad Hughes, MD
Especialista en cirugía cardíaca
Número de Protocolo
IRB: PRO00119673
NCT: NCT07166133
Fase
Fase N/A
ClinicalTrials.gov
Estado de inscripción
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Contribuya a Duke Health