drugset / Trial / NCT00399542

Efficacy and Safety of Lubiprostone in Patients With Irritable Bowel Syndrome With Constipation

NCT00399542 ↗

RandomizedParallel-groupDouble-blindTreatment

Summary

The primary purpose of this study is to evaluate the efficacy and safety of administration of lubiprostone in patients with irritable bowel syndrome with constipation.

Timeline

Start
2005-05
Primary completion
2006-07
Completion
2006-07

Outcome

Met primary endpoint

registry NUMBER Lubiprostone: 12.1 percentage of participants NUMBER Placebo: 5.7 percentage of participants analysis (unspecified test); Lubiprostone vs Placebo; p = 0.023; NCT00399542 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Lubiprostone Small molecule — —