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Negative Pressure Wound Therapy for Surgical Site Infection Prevention in Common Femoral Artery Exposure

Surgical Site Infection Clinical Trial

Official title:
Negative Pressure Wound Therapy for Surgical Site Infection Prevention in Vascular Surgery Patients Undergoing Common Femoral Artery Exposure

Clinical Trial Summary

The purpose of this randomized clinical trial is to investigate the role of negative pressure wound therapy (NPWT) vs standard sterile gauze therapy on the incidence of surgical site infections (SSI) in primarily closed groin incisions in high risk patients undergoing any open common femoral artery exposure for a vascular surgery procedure.

Clinical Trial Description

Eligible patients are randomized pre-operatively into either a standard dressing or NPWT for the groin incision. - 1 The control group receive a standard sterile gauge dressing over the groin incision. The dressing is removed on post-operative day #2 and the wound is inspected for a SSI or dehiscence, followed by daily dressing changes and wound inspections until discharge. - 2 The intervention group will receive a NPWT dressing which will be applied in the operating room under sterile conditions. The NPWT dressing will be removed on Post operative day 5. The wound is inspected for a SSI or dehiscence, followed by daily dressing changes and wound inspections until discharge. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03935659
Study type Interventional
Source Henry Ford Health System
Contact
Status Withdrawn
Phase N/A
Start date March 26, 2018
Completion date October 1, 2021
View Details
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