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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


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

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