drugset / Trial / NCT01267942

Intravenous Enhancin[Co-amoxiclav] Versus Postoperative Enhancin in Prevention of Postadenotonsillectomy Morbidity.

NCT01267942

Completed 126 enrolled University of Nairobi
RandomizedParallel-groupSingle-blindPrevention

Summary

Null hypothesis; The efficacy of Enhancin\]Co-Amoxiclav given as a single intravenous dose at induction is not better than a five days oral course of the same given postoperatively in reducing postoperative morbidity after adenotonsillectomy.

Timeline

Start
2008-05
Primary completion
2008-10
Completion
2009-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Amoxicillin Other / unclassified 25 mg/kg Intravenous

Indications