Trials / Completed
CompletedNCT00092170
An Investigational Agent for the Treatment of Complicated Intra-Abdominal Infections or Acute Pelvic Infections (0826-038)
A Prospective, Multicenter, Randomized, Open-Label, Comparative Study to Evaluate the Safety, Tolerability, and Efficacy of Ertapenem Sodium ( MK0826) Versus Ticarcillin/Clavulanate in the Treatment of Hospital-Acquired Pneumonia, Complicated Intra-Abdominal Infections, and Acute Pelvic Infections in Pediatric Patients
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 100 (planned)
- Sponsor
- Merck Sharp & Dohme LLC · Industry
- Sex
- All
- Age
- 3 Months – 17 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to determine the effect of an approved medication for adults for an investigational use in pediatric patients 3 months to 17 years for the treatment of complicated intra-abdominal infections or acute pelvic infections.
Detailed description
The duration of treatment is 18 months.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | MK0826, ertapenem sodium | |
| DRUG | Comparator: Ticarcillin/Clavulanate |
Timeline
- Start date
- 2002-03-01
- Primary completion
- 2004-01-01
- Completion
- 2004-01-01
- First posted
- 2004-09-24
- Last updated
- 2017-02-17
Source: ClinicalTrials.gov record NCT00092170. Inclusion in this directory is not an endorsement.