Thoraflex EXTEND (Stress Management for People with Heart Disease) - Clinical Trial
Email to Participate
hillary.hood@duke.edu
What is the Purpose of this Study?
If you agree to be in this study you will:
- Have your aorta repaired with the Thoraflex Hybrid device
- Have information collected from your medical record
- Have study visits for up to 10 years after your aortic repair surgery (some may be completed via phone)
What is the Condition Being Studied?
Aortic Disease
Who Can Participate in the Study?
Adults requiring surgical repair of their aorta.
Grupo etario
Adultos
What is Involved?
We are doing this study to collect information on the use of the Thoraflex Hybrid device to treat aortic disease.
Study Details
Full Title
Thoraflex Hybrid and Relay Extension Post-Approval Study (EXTEND)
Principal Investigator
Especialista en cirugía cardíaca
Protocol Number
IRB:
PRO00112349
NCT:
NCT05639400
Phase
Phase
N/A
ClinicalTrials.gov
View on ClinicalTrials.gov
Estado de inscripción
Abierto para inscripción
Participate
Email hillary.hood@duke.edu