drugset / Trial / NCT01473836
A Phase 3 Study Of Intravenous Metronidazole For Intrabdominal Infection
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ceftriaxone | Other / unclassified | 2 g | Intravenous |
| Subject | Ceftriaxone | Other / unclassified | 4 g | Intravenous |
| Subject | Metronidazole | Small molecule | 500 mg | Intravenous |