drugset / Trial / NCT00368498

A Trial to Evaluate the Loading Dose Required to Achieve Therapeutic Serum Teicoplanin Concentration Timely

NCT00368498

Phase 4 Unknown 20 enrolled National Taiwan University Hospital
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study is to determine whether the standard dosage of teicoplanin is adequate to produce timely the trough level \> 10 mg/L, which is considered to be effective in the treatment of methicillin-resistant Staphyllococcus aureus (MRSA) bacteremia.

Timeline

Start
2006-06
Primary completion
Completion
2007-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Teicoplanin Other / unclassified 6 mg/kg
Subject Teicoplanin Other / unclassified 12 mg/kg