Surgical Infection Rates With Adjunct Vancomycin Compared to Standard Peri-Operative IV Antibiotics

Lumbar Pain Clinical Trial

Official title:
Surgical Infection Rates With Adjunct Vancomycin Compared to Standard Peri-Operative IV Antibiotics

Status Recruiting

Clinical Trial Summary

Determine the effect of Vancomycin Powder added to the surgical wound at closure on surgical infection rates.

Clinical Trial Description

Study will be blinded and randomized 1:1 to either Vancomycin Powder at closure or no vancomycin powder at closure. ;

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Subject), Primary Purpose: Prevention

Related Conditions & MeSH terms

Lumbar Pain

Clinical Trial Details

NCT number	NCT02299882
Study type	Interventional
Source	Spectrum Health Hospitals
Contact
Status	Recruiting
Phase	N/A
Start date	August 2012
Completion date	January 2016

View Details

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