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Intra-wound Vancomycin Powder for Prevention of Surgical Site Infection Following Spinal Surgery

Infection Clinical Trial

Official title:
Intra-wound Vancomycin Powder for Prevention of Surgical Site Infection Following Spinal Surgery - a Randomized Controlled Superiority Trial

Clinical Trial Summary

Cefazolin is given routinely pre and intraoperatively for patients undergoing spinal surgery to reduce the rate of infection. Intra-wound admission of Vancomycin powder has been suggested to reduce wound infection rates. Therefore, this study aims to compare the rate of wound-related complications between patients receiving standard treatment compared to patients receiving an addition of topical Vancomycin and to identify the optimal Vancomycin dosage. All groups will receive the recommended regimen of routine IV antibiotic prophylaxis.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05959603
Study type Interventional
Source Rabin Medical Center
Contact Eyal Itshayek, MD
Phone +972-50-8946921
Email eyal.itshayek@gmail.com
Status Recruiting
Phase Phase 3
Start date May 31, 2020
Completion date December 1, 2025
View Details
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