Trial intelligence / Profile preview

Efficacy of Prucalopride in Critically Ill Patients With Paralytic Ileus

NCT04190173Phase 3Unknown

Sponsor
Prince of Songkla University
Start
Jul 2017
Primary completion
Jan 2020
Modality
Small Molecules
Countries
1
01

Overview

Phase 3, randomised, double-blind trial in paralytic ileus comparing Prucalopride with Placebo (2 arms). Primary endpoint: Change of maximum bowel diameter from baseline at 120 hours. Status: unknown.

02

Drugs

prucalopride
03

Conditions

paralytic ileus

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