Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis

AAA - Abdominal Aortic Aneurysm Clinical Trial

Official title:
Assessment of Long Term, Endovascular AAA Intervention Using the GORE® EXCLUDER® Conformable AAA Endoprosthesis or Iliac Branch Endoprosthesis

Status Recruiting

Clinical Trial Summary

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.

Clinical Trial 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. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06218875
Study type	Observational [Patient Registry]
Source	W.L.Gore & Associates
Contact	K Martin
Phone	928-864-2223
Email	kgmartin@wlgore.com
Status	Recruiting
Phase
Start date	May 7, 2024
Completion date	September 30, 2042

View Details

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