Evaluation of GORE® VIABAHN® Endoprosthesis for Popliteal Artery Aneurysm

Stopped early

Conditions studied: Popliteal Artery Aneurysm

In brief

This is a multicenter, non-randomized, single arm, retrospective study of GORE® VIABAHN® Endoprosthesis for the treatment of a Popliteal Artery Aneurysm (PAA).

Key facts

Study ID

NCT01902888

Run by

W.L.Gore & Associates

People needed

3

Starts

2013-07-01

Expected to finish

2014-04-01

Last updated by the study team

2015-06-19

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Received a GORE® VIABAHN® Endoprosthesis between January 1, 2002 and December 31, 2010 to treat a popliteal artery aneurysm;
• Had an asymptomatic aneurysm (≥ 2 cm diameter) of the popliteal artery, or symptomatic aneurysm (no diameter requirement) of the popliteal artery, or the presence of mural thrombus (no diameter requirement) of the popliteal artery;
• Was 18 years of age or older; and
• Had an elective popliteal artery aneurysm procedure.

You may not qualify if…

• Bilateral popliteal artery aneurysms with initial treatment on the same day
• Had previous surgery for the popliteal artery aneurysm in the study limb

Where it is running

• Baptist Health — Miami, Florida, United States
• The Vascular Group of Naples — Naples, Florida, United States
• Washington University School of Medicine — St Louis, Missouri, United States

Full record on ClinicalTrials.gov

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