drugset / Trial / NCT01473836

A Phase 3 Study Of Intravenous Metronidazole For Intrabdominal Infection

NCT01473836

Phase 3 Completed 38 enrolled Pfizer
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the clinical efficacy and safety in Japanese adult subjects with Intra-abdominal/Pelvic infections receiving Metronidazole IV 1,500-2,000 mg/day in combination with ceftriaxone sodium.

Timeline

Start
2011-11
Primary completion
2012-10
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Ceftriaxone Other / unclassified 2 g Intravenous
Subject Ceftriaxone Other / unclassified 4 g Intravenous
Subject Metronidazole Small molecule 500 mg Intravenous