Treatment of Patients With Traumatic or Iatrogenic Vessel Injuries

W.L. Gore & Associates

Status: Completed

Conditions: Iatrogenic Vessel Injury

Treatments: Device: GORE® VIABAHN® Endoprosthesis

Study type: Observational

Funder types: Industry

Identifiers

NCT05183399

JPS 16-04

Details and patient eligibility

About

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).

Enrollment: 30 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Patients with traumatic or iatrogenic vessel injuries in thoracic, abdominal, and pelvic arteries (except the aorta, coronary, brachiocephalic, carotid, vertebral and pulmonary arteries ) with a reference vessel diameter ranging from 4.0 to 12.0mm.