drugset / Trial / NCT00575614

Prucalopride in Patients With Chronic Idiopathic Constipation

NCT00575614

Phase 2 Completed 87 enrolled Movetis
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to determine whether prucalopride is safe and effective in the treatment of chronic idiopathic constipation. Hypothesis: Prucalopride given at a dose of 1 mg o.d. for 4 weeks to female patients with chronic constipation shows a favourable effect on most of the efficacy parameters assessed in this trial. This dosage can be considered safe and generally well-tolerated.

Timeline

Start
1997-04
Primary completion
1999-03
Completion
1999-03

Drugs

EvaluationDrugModalityDoseRoute
Comparator Prucalopride Small molecule 1 mg

Indications