The purpose of the study is to determine whether a single, pre-operative dose of cefuroxime is effective in preventing surgical site infection in patients undergoing surgery for herniated disk
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
QUADRUPLE
Enrollment
1,369
preoperative intravenous 1.5g cefuroxime
preoperative intravenous placebo
Hôpitaux Universitaire de Genève
Geneva, Switzerland
Centre Hospitalier Universitaire Vaudois
Lausanne, Switzerland
Occurrence of a surgical site infection
Time frame: 6 months
Occurrence of a post-operative infection other than surgical site infection
Time frame: 6 monts
Serious adverse event
Time frame: 6 months
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