The Effect of Intrawound Vancomycin Powder in Spine Surgery

Recruiting Phase 4 Interventional Study
Spine Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
18 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Prevention
Participants needed
1,643 (estimated)
Sponsor
Windsor-Essex Compassionate Care Community · Other
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About This Trial
Problem: Postoperative wound infection following various spinal surgeries is a serious complication. The incidence of post-surgical wounds in spine surgery is high, and various researchers have reported different infection rates. In addition, increased healthcare costs, prolonged lengths of stay in hospital, and reduced quality of life as a result of surgical site infections (SSI) are also major c…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Patients requiring surgery due to any spine disease. Exclusion Criteria: * A previous history of infections at the spine surgical site. * Biopsy procedure. * Patients with a postoperative follow-up time of less than 12 weeks. * Patients allergic to vancomycin. * Patient is l…
Contacts

Mohamed Soliman, MSc, MD

17329241637

msolim8@uwo.ca

CONTACT

Abdalla Shamisa, FRCSC

ashamisa@yahoo.ca

CONTACT