Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis
Purpose
A prospective, observational post-market registry collecting outcomes through a 10-year post procedure follow-up for patients treated with the GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) or the GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device) as a part of routine clinical practice.
Condition
- AAA - Abdominal Aortic Aneurysm
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- Patient or legally authorized representative (LAR) provides written authorization and/or consent per institution and geographical requirements 2. Patient has been or is intended to be treated with an eligible registry device 3. Patient is age ≥ 18 years at time of informed consent signature.
Exclusion Criteria
- Patient who is, at the time of consent, unlikely to be available for standard of care (SOC) follow-up visits as defined by the site's guidelines and procedures. 2. Patient with exclusion criteria required by local law. 3. Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study within 12 months of Together Registry enrollment. Subjects cannot be enrolled in another Together Registry module protocol.
Study Design
- Phase
- Study Type
- Observational [Patient Registry]
- Observational Model
- Cohort
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| GORE® EXCLUDER® Conformable AAA Endoprosthesis (EXCC Device) | Patients treated with the EXCC Device | |
| GORE® EXCLUDER® Iliac Branch Endoprosthesis (IBE Device) | Patients treated with the IBE Device |
Recruiting Locations
Little Rock, Arkansas 72205
Irvine, California 92697
Los Angeles, California 90033
Los Angeles, California 90033
Palo Alto, California 94304
Stanford, California 94304
Miami Beach, Florida 33140
Atlanta, Georgia 30033
Atlanta, Georgia 30322
Augusta, Georgia 30912
Decatur, Georgia 30033
Chicago, Illinois 60637
Indianapolis, Indiana 46260
Louisville, Kentucky 40202
Baton Rouge, Louisiana 70808
Baltimore, Maryland 21201
Boston, Massachusetts 02215
Boston, Massachusetts 02215
Bay City, Michigan 48708
Grand Rapids, Michigan 49546
Minneapolis, Minnesota 55407
Columbia, Missouri 65212
Springfield, Missouri 65807
Lebanon, New Hampshire 03766
Lebanon, New Hampshire 03766
Buffalo, New York 14203
Asheville, North Carolina 28801
Chapel Hill, North Carolina 27599
Durham, North Carolina 27710
Durham, North Carolina 27710
Winston-Salem, North Carolina 27103
Winston-Salem, North Carolina 27157
Winston-Salem, North Carolina 27157
Cleveland, Ohio 44106
Portland, Oregon 97239
Portland, Oregon 97239
Philadelphia, Pennsylvania 19104
Philadelphia, Pennsylvania 19104
Greenville, South Carolina 29615
Greenville, South Carolina 29615
Dallas, Texas 75390
Plano, Texas 75075
Plano, Texas 75093
Salt Lake City, Utah 84112
Salt Lake City, Utah 84112
Falls Church, Virginia 22042
Norfolk, Virginia 23507
Norfolk, Virginia 23507
Charleston, West Virginia 25304
Milwaukee, Wisconsin 53226
More Details
- NCT ID
- NCT06218875
- Status
- Recruiting
- Sponsor
- W.L.Gore & Associates
Detailed Description
The purpose of the Gore Together Aortic Registry is to collect real-world data (RWD) for Gore aortic endovascular devices. Due to the nature of the program, patient selection, diagnostic imaging, and treatment interventions will be determined by physicians based on standard clinical practice. Therefore, the Sponsor will not be outlining requirements that would influence healthcare decisions. Participants will be asked to return for regular scheduled visits as requested by their surgeon. Patients will report any issues they may have regarding the device or surgery to their surgeon/doctor.