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Study identifier: NCT05959603 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

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

Condition: Infection  ·  Sponsor: Rabin Medical Center

PhasePhase 3
Planned participants363
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersNo

About this study

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.

This description comes directly from the study's public registry record.

Talk to the study team

Eyal Itshayek, MD  ·  +972-50-8946921  ·  eyal.itshayek@gmail.com

Shani Berkowitz, Msc  ·  +972528620737  ·  shanihberkowitz@gmail.com

Always discuss trial participation with your own doctor first.

Locations (1)

Rabin Medical CenterPetah Tikva, IsraelRecruiting

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Source record: clinicaltrials.gov/study/NCT05959603