drugset / Trial / NCT00232089

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

NCT00232089

Phase 3 Completed 1296 enrolled Novartis
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

EvaluationDrugModalityDoseRoute
Subject Tegaserod Small molecule 6 mg

Indications