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Clinical Trial Summary

Groin incisions in vascular surgery have complications in up to 30% of cases at 30 days, resulting in reductions in patient quality of life and increased costs. Prior attempts at reducing this complication rate have been largely unsuccessful. The purpose of this study is to determine the feasibility of routine Vialize use for vascular surgeries involving a groin incision and to determine the rates of surgical site infection/dehiscence in such patients receiving subcutaneous Vialize.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06032949
Study type Interventional
Source University of Florida
Contact Tam Nguyen
Phone 352-273-5482
Email tam.nguyen@surgery.ufl.edu
Status Recruiting
Phase N/A
Start date October 23, 2023
Completion date October 2024

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