Trials / Completed
CompletedNCT00389987
Ertapenem Sodium vs. Piperacillin/Tazobactam in the Treatment of Complicated Intra-Abdominal Infections (0826-037)
A Prospective, Multicenter, Double-Blind With In-House Blinding, Randomized, Comparative Study to Evaluate the Efficacy, Safety, and Tolerability of Ertapenem Sodium Versus Piperacillin/Tazobactam in the Treatment of Complicated Intra-Abdominal Infections in Hospitalized Adults
- Status
- Completed
- Phase
- Phase 3
- Study type
- Interventional
- Enrollment
- 300 (planned)
- Sponsor
- Merck Sharp & Dohme LLC · Industry
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
This study is designed to compare the efficacy of ertapenem and piperacillin/tazobactam with respect to the clinical response in baseline microbiologically evaluable patients; and to evaluate the tolerability and safety of ertapenem compared to piperacillin/tazobactam.
Detailed description
Original label approved November 2001
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | MK0826, /Duration of Treatment : 8 Weeks | |
| DRUG | Comparator : piperacillin sodium (+) tazobactam sodium /Duration of Treatment : 8 Weeks |
Timeline
- Start date
- 2001-09-01
- Primary completion
- 2004-05-01
- Completion
- 2004-05-01
- First posted
- 2006-10-19
- Last updated
- 2017-02-17
Source: ClinicalTrials.gov record NCT00389987. Inclusion in this directory is not an endorsement.