Status:
COMPLETED
Treatment of Patients With Traumatic or Iatrogenic Vessel Injuries
Lead Sponsor:
W.L.Gore & Associates
Conditions:
Iatrogenic Vessel Injury
Eligibility:
All Genders
Brief 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, ...
Eligibility Criteria
Inclusion
- 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.
Exclusion
Key Trial Info
Start Date :
December 1 2016
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
February 14 2021
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT05183399
Start Date
December 1 2016
End Date
February 14 2021
Last Update
January 10 2023
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