drugset / Trial / NCT03190668

Skeletal Muscle and Adipose Tissue Study

NCT03190668

Phase 4 Completed 12 enrolled University of Florida
RandomizedParallel-groupOpen-labelPrevention

Summary

The purpose of this research study is to compare the current standard of care for prophylactic Cefazolin administered every 3 hours intravenously with continuous infusion of Cefazolin during pediatric spinal surgery.

Timeline

Start
2018-05-29
Primary completion
2022-06-23
Completion
2022-06-23

Drugs

EvaluationDrugModalityDoseRoute
Comparator Cefazolin Small molecule 10 mg/kg Intravenous
Comparator Cefazolin Small molecule 30 mg/kg Intravenous

Indications