ARISE II (Ascending Aorta Repair) - Clinical Trial
Email to Participate
susan.hajmohammad@duke.edu
What is the Purpose of this Study?
We are doing this study to determine the safety and effectiveness of an experimental medical device called the GORE Ascending Stent Graft (ASG Device) for the treatment of aortic diseases.
What is the Condition Being Studied?
Aortic Disease
Who Can Participate in the Study?
Adults ages 18+ who plan to have surgical repair made to their ascending aorta.
For more information about who can join this study, contact the study team at susan.hajmohammad@duke.edu.
Age Group
Adults
What is Involved?
If you agree to be in this study, you will:
- Have your aorta repaired with the GORE Ascending Stent Graft (ASG Device)
- Have neurological assessments
- Have CT scans
- Fill out questionnaires
- Give the study team permission to collect information from your medical record
Study Details
Full Title
Evaluation of the GORE® Ascending Stent Graft in the Treatment of Lesions of the Ascending Aorta (ARISE II)
Principal Investigator
Heart Surgeon
Protocol Number
IRB:
PRO00113653
NCT:
NCT05800743
Phase
Phase
N/A
ClinicalTrials.gov
View on ClinicalTrials.gov
Enrollment Status
Open for Enrollment
Participate