drugset / Trial / NCT00232089
Assessment of Efficacy and Safety of Tegaserod Treatment and Placebo in Women With Dyspepsia
RandomizedParallel-groupDouble-blindTreatment
Summary
This study is being done to evaluate the safety, tolerability and satisfactory relief of dyspepsia symptoms in females excluding those with predominant stomach pain. Tegaserod will be evaluated at 6mg twice daily and placebo.
Timeline
- Start
- 2004-05
- Primary completion
- 2006-06
- Completion
- 2006-06
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Tegaserod | Small molecule | 6 mg | — |