ARISE II (Ascending Aorta Repair) - Clinical Trial

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

Age Group

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
Protocol Number
IRB: PRO00113653
NCT: NCT05800743
Phase N/A
Enrollment Status
Open for Enrollment