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Study identifier: NCT05811364 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

The GORE VBX FORWARD Clinical Study: A Comparison of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis to Bare Metal Stenting for Patients With Complex Iliac Occlusive Disease

Condition: Aortoiliac Occlusive Disease · Peripheral Arterial Disease  ·  Sponsor: W.L.Gore & Associates

PhaseNA
Planned participants244
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objective of this prospective, multicenter, randomized, controlled clinical trial is to demonstrate the superiority of the VBX Device for primary patency when compared to bare metal stenting in complex iliac occlusive disease.

This description comes directly from the study's public registry record.

Talk to the study team

Alexander Ambrocik  ·  337-387-4954  ·  aambroc@wlgore.com

Enoque Costa  ·  928-525-4044  ·  ecosta@wlgore.com

Always discuss trial participation with your own doctor first.

Locations (43)

Central Arkansas Veterans Healthcare SystemLittle Rock, Arkansas, United StatesWithdrawn
VA Long Beach Healthcare SystemLong Beach, California, United StatesRecruiting
Denver Health and Hospital AuthorityDenver, Colorado, United StatesRecruiting
North Suburban Medical CenterDenver, Colorado, United StatesWithdrawn
University of Florida - GainesvilleGainesville, Florida, United StatesRecruiting
Radiology and Imaging Specialists of LakelandLakeland, Florida, United StatesRecruiting
University of South FloridaTampa, Florida, United StatesRecruiting
Atlanta VA Medical CenterDecatur, Georgia, United StatesRecruiting
Louisiana State University Health Sciences CenterNew Orleans, Louisiana, United StatesRecruiting
Beth Israel Deaconess Medical Center, Inc.Boston, Massachusetts, United StatesRecruiting
Corewell Health SystemGrand Rapids, Michigan, United StatesRecruiting
The Curators of the University of MissouriColumbia, Missouri, United StatesRecruiting

+ 31 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05811364