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Assessment of Efficacy and Safety of Tegaserod Treatment and Placebo in Women With Dyspepsia

Dyspepsia Clinical Trial

Official title:
Assessment of Efficacy and Safety of Tegaserod Treatment and Placebo in Women With Dyspepsia

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00232024
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date January 2004
Completion date May 2006
View Details
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