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Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia

Dyspepsia Clinical Trial

Official title:
Extension Study to Assess the Long-Term Safety of Tegaserod in Women With Symptoms of Dyspepsia

Clinical Trial Summary

This study is being done to evaluate the long-term safety of tegaserod in women with symptoms of dyspepsia who have completed the core study. Tegaserod will be evaluated at 6 mg twice daily.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00232102
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date September 2004
Completion date August 2006
View Details
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