Gore Registry TGR 23-02AA (Aorta and Iliac Artery Stent-Grafts) - Clinical Trial
What is the Purpose of this Study?
We are using this registry to gather data about the use and safety of certain medical devices used in a part of the body called the aorta and/or iliac arteries, which are large blood vessels that run inside the chest, abdomen, and groin area. The name of the devices being looked at are the GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) or the GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device).
Aorta and Iliac Artery Stent-Grafts
Who Can Participate in the Study?
Adults ages 18+ who have surgery at Duke to get the GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) or the GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device).
For more information about this study, contact the team at frank.benedetti@duke.edu.
What is Involved?
Following discharge from the hospital, your doctor or a staff member may call you occasionally to ask how you are doing in terms of health. This could include questions about the need for additional surgical procedures, confirm that the registry device has not been removed, or any other important medical conditions that could be helpful in the follow-up of your registry procedure. Being in the registry will let the study doctor enter information about your medical history, surgery, and results of follow-up testing into a computer program.
Study Details
