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Clinical Trial ● Currently Recruiting NCT06872905

Real-World Data Collection of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis When Used in Covered Endovascular Reconstruction of the Aortic Bifurcation (CERAB) to Treat Aortoiliac Occlusive Disease

Real-World Data Collection of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis When Used in Covered Endovascular Reconstruction of the Aortic Bifurcation (CERAB) to Treat Aortoiliac Occlusive Disease —…

📅 30 Mar 2026 ⏱ 1 min read
Currently Recruiting
This trial is actively seeking participants in the UK. Discuss eligibility with your patient before referring.
Status
Currently Recruiting
NCT ID
NCT06872905
Start
2025-05-30
Completion
2027-08-16
ClinicaliQ Trial Snapshot
  • Real-World Data Collection of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis When Used in Covered Endovascular Reconstruction of the Aortic Bifurcation (CERAB) to Treat Aortoiliac Occlusive Disease — Recruiting • NCT06872905.
  • Review the linked registry entry for study design, population, endpoints, and operational status.

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What This Trial Is Studying

The study will assess the safety and effectiveness of the GORE® VIABAHN® VBX Balloon Expandable Endoprosthesis ("VBX Device" or also referred to as "VBX Stent Graft") in a post approval setting and evaluate the quality of the use in covered endovascular reconstruction of the aortic bifurcation (CERAB) to treat Aortoiliac Occlusive Disease (AIOD). Conditions: Aortoiliac Occlusive Disease Interventions: GORE VIABAHN® VBX Balloon Expandable Endoprosthesis (VBX) Lead Sponsor: W.L.Gore & Associates Planned Enrollment: 158 participants

Full Trial Details
View this trial on the source registry
Eligibility criteria, protocol, and results when available
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