Prevena Spine for Use in Spine Surgery

Status Recruiting

Clinical Trial Summary

A pilot, prospective, single-center study for the investigation of the use of Prevena Vacuum-Assisted Closure devices in patients undergoing spine surgery.

Clinical Trial Description

The objective of the study is to evaluate the efficacy of the Prevena Plus 125 therapy Unit (KCI USA, Inc.) in preventing surgical site infections and other wound complications in patients undergoing spine surgery compared to conventional wound dressing. Furthermore, the investigators want to illustrate which patients benefit most significantly from Prevena usage as spine surgery sees a range of potential candidates, and not all may experience equivalent recovery from spine surgery with Prevena intervention. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05555355
Study type	Interventional
Source	Northwestern University
Contact	Robert Galiano, MD
Phone	312-695-6022
Email	robert.galiano@nm.org
Status	Recruiting
Phase	Phase 4
Start date	December 1, 2022
Completion date	October 1, 2024

View Details

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