Irritable Bowel Syndrome Clinical Trial
Official title:
A Phase III Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study of Renzapride in Women With Constipation-Predominant Irritable Bowel Syndrome (c-IBS)
The purpose of the study is to investigate whether renzapride will help alleviate the symptoms associated with constipation predominant irritable bowel syndrome in female patients.
Irritable bowel syndrome (IBS) is a chronic gastrointestinal disorder characterized by
recurrent symptoms of abdominal pain/discomfort accompanied by disturbed bowel function.
In this study female patients with constipation predominant IBS will receive one of two
dosing regimens of renzapride or placebo for 12 weeks. Patients will record the severity of
their symptoms throughout the study. The results will be analysed to see if those patients
who received renzapride had greater relief of their symptoms than did the patients who
received placebo.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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