Trials / Completed
CompletedNCT00136201
Study Comparing Tigecycline and Imipenem/Cilastatin in Chinese Subjects With Complicated Intra-Abdominal Infections
A Multicenter, Randomized, Open-Label Comparison of the Safety and Efficacy of Tigecycline> vs Imipenem/Cilastatin to Treat Complicated Intra-Abdominal Infections in Hospitalized Chinese Subjects
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 200 (planned)
- Sponsor
- Wyeth is now a wholly owned subsidiary of Pfizer · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The primary objective of this study is to compare the safety and efficacy of an experimental antibiotic to a marketed antibiotic in the treatment of Chinese subjects with complicated intra-abdominal infections. \<br /\>
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | tigecycline |
Timeline
- Start date
- 2005-11-01
- Primary completion
- 2006-12-01
- Completion
- 2006-12-01
- First posted
- 2005-08-26
- Last updated
- 2009-07-07
Locations
11 sites across 1 country: China
Source: ClinicalTrials.gov record NCT00136201. Inclusion in this directory is not an endorsement.