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).
Who Can Participate?
Eligibility
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.
Age Range
18-110
Sex/Genders
Male (cisgender)
Female (cisgender)
Non-binary or gender fluid
Transgender male
Transgender female
Looking for Healthy Participants
No
What is Involved?
Description
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.
Locations
Duke University Hospital
Duke Regional Hospital
Duke Raleigh Hospital
Visit Timing
Weekdays
Compensation
No
Spanish Materials Available
No
Study Details
Full Title
Assessment of Long Term, Endovascular AAA Intervention using the Gore® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis
Principal Investigator
Chandler
Long
Protocol Number
PRO00115788
Phase
N/A
Enrollment Status
Pending Open to Enrollment