A Post Marketing Surveillance Study on the Safety and Effectiveness of Prucalopride in the Treatment of Chronic Constipation

• Status: Withdrawn
• Trial end date: 2014-12-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to determine the safety and effectiveness of prucalopride in the treatment of Filipino patients with chronic constipation whom prior laxatives fail to provide adequate relief.

• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Janssen Pharmaceutica
• Treatments: Prucalopride

Criteria

Inclusion Criteria:

• Diagnosis of chronic constipation by history and physical examination, including rectal exam

• History of chronic constipation not satisfied with laxatives

• Patient reports, on average, 2 or fewer spontaneous bowel movements (SBMs) per week and 1 or more of the following for the last three months: very hard (little balls) and/or hard stools in more than 25% of bowel movements (BMs); sensation of incomplete evacuation in more than 25% of BMs; straining at defecation in more than 25% of BMs; sensation of ano-rectal obstruction or blockade in more than 25% of BMs; a need for digital manipulation to facilitate evacuation in more than 25% of BMs

• Females of childbearing potential agree to use highly effective contraceptive methods

Exclusion Criteria:

• Renal impairment requiring dialysis

• Secondary chronic constipation and organic gastrointestinal (GI) disorders

• Intestinal perforation / obstruction due to structural or functional disorder of the gut wall, obstructive ileus, severe inflammatory condition of the intestinal tract such as Crohn's disease, ulcerative colitis, toxic megacolon / rectum

• Hypersensitive to Prucalopride or to any of its components

• Patients receiving concomitant drugs known to cause QTc prolongation

• Pregnant or lactating