Clinical Trials Directory

Trials / Completed

CompletedNCT01883999

Evaluation of the GORE® EXCLUDER® Iliac Branch Endoprosthesis

Evaluation of the GORE® EXCLUDER® Iliac Branch Endoprosthesis for the Treatment of Common Iliac Artery Aneurysms or Aorto-iliac Aneurysms

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
64 (actual)
Sponsor
W.L.Gore & Associates · Industry
Sex
All
Age
21 Years
Healthy volunteers
Not accepted

Summary

The Iliac Branch Endoprosthesis (IBE) 12-04 study will be a prospective, nonrandomized, multicenter, single-arm evaluation designed to assess the safety and efficacy of the IBE Device in subjects with common iliac artery aneurysms (CIAA) or aorto-iliac aneurysms (AIA).

Conditions

Interventions

TypeNameDescription
DEVICEGORE® EXCLUDER® Iliac Branch Endoprosthesis

Timeline

Start date
2013-10-01
Primary completion
2016-04-01
Completion
2021-06-01
First posted
2013-06-21
Last updated
2021-11-02
Results posted
2016-08-03

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01883999. Inclusion in this directory is not an endorsement.