Ensayo clínico

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

NCT: NCT05811364 · RECRUITING

ID NCTNCT05811364

EstadoRECRUITING

Fecha de inicio2023-10-17

Finalización2032-01-31

SponsorW.L.Gore & Associates (INDUSTRY)

First posted2023-04-13

Last updated2026-05-13

Resumen breve

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.

Fuente oficial

Ver en ClinicalTrials.gov →

Datos obtenidos de la API de ClinicalTrials.gov. Para conocer el estado más reciente, consulte el registro oficial.