Treatment of Patients With Traumatic or Iatrogenic Vessel Injuries
NCT05183399 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 30
Last updated 2023-01-10
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).
Conditions
- Iatrogenic Vessel Injury
Interventions
- DEVICE
-
GORE® VIABAHN® Endoprosthesis
Sponsors & Collaborators
-
W.L.Gore & Associates
lead INDUSTRY
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-12-01
- Primary Completion
- 2017-05-19
- Completion
- 2021-02-14
- FDA Device
- Yes
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