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Reduction of Groin Wound Infections After Vascular Surgery by Using an Incision Management System (IMS) — IMS  

Infections Clinical Trial

Official title:
Reduction of Groin Wound Infections After Vascular Surgery in Patients With Risk Factors by the Use a Negative Pressure Wound Incision Management System (KCI Prevena)

Clinical Trial Summary

Comparison of the Prevena™ IMS with the standard wound management method of sterile plaster in vascular surgery patients.

Clinical Trial Description

Comparison of the Prevena™ IMS with the standard wound management method of sterile plaster in vascular surgery patients.

The aim is to demonstrate that the application of the Prevena™ IMS significantly reduces the incidence of postoperative wound infections. The wound infections will be classified according to Szilagyi.

The treatment phase begins following vascular surgery with wound management using either the Prevena™ IMS or a standard wound dressing, depending on the group to which the patient was randomly assigned. It involves a minimum stay of 7 and maximum 10 days in hospital. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02395159
Study type Interventional
Source RWTH Aachen University
Contact
Status Completed
Phase N/A
Start date July 2015
Completion date October 10, 2017
View Details
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