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Skeletal Muscle and Adipose Tissue Study

Idiopathic Scoliosis Clinical Trial

Official title:
Skeletal Muscle and Adipose Tissue Concentrations of Cefazolin Comparing Two Different Dosing Regimens During Pediatric Posterior Spinal Fusion Surgery

Clinical Trial 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.

Clinical Trial Description

Determine the skeletal muscle and adipose tissue disposition of prophylactic Cefazolin using microdialysis sampling in a cohort of patients diagnosed with idiopathic scoliosis undergoing posterior spinal fusion (PSF) for administration of Cefazolin by either continuous infusion or intermittent bolus. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT03190668
Study type Interventional
Source University of Florida
Contact
Status Completed
Phase Phase 4
Start date May 29, 2018
Completion date June 23, 2022
View Details
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