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Clinical Trial Summary

The purpose of this study is to confirm device efficacy and safety of the GORE® VIABAHN® Endoprosthesis (hereafter "VB device") for the treatment of traumatic or iatrogenic vessel injury in thoracic, abdominal, and pelvic arteries (except the aorta, coronary, brachiocephalic, carotid, vertebral and pulmonary arteries).

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05183399
Study type Observational
Source W.L.Gore & Associates
Status Completed
Start date December 1, 2016
Completion date February 14, 2021