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Groin Wound Infection Rate Using Prevena Compared to Standard Dressing in Vascular Surgery Patients With High Risk — PREVENA  

Endovascular Procedures Clinical Trial

Official title:
Experience With the Negative Pressure Incision Management System (Prevena) in Vascular Surgery Patients With High Risk for Groin Wound Infection

Clinical Trial Summary

Evaluate wound healing using Prevena compared to standard dressings in high risk patients after vascular surgery.

Clinical Trial Description

Patients submitted to bilateral femoral endarterectomy will have one groin dressed with PrevenaTM and the contralateral one dressed with conventional bandage immediately after suture. Both PrevenaTM and the conventional bandage at the contralateral side will be removed before the patient discharge. Groin wound complications such as deep space infection, cutaneous cellulitis, dehiscence or re-interventions for wound-related complications will be observed in a 30-day evaluation window. This observation will be performed during the patient admission and in the post-operative standard of care visits among the first 30 days. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03105154
Study type Interventional
Source The Cleveland Clinic
Contact
Status Completed
Phase N/A
Start date February 2016
Completion date November 10, 2020
View Details
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