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NCT00793247

A Double-Blind, Placebo-Controlled, Cross-Over, Multiple (n=1) Trial to Evaluate the Effects of R093877 in Patients With Chronic Intestinal Pseudo-Obstruction (CIP).

Completed Phase 2 Last updated 18 November 2008
What this trial tests

Phase 2 trial testing PRU-PLA-PRU-PLA in Chronic Intestinal Pseudo-Obstruction. Completed.

Quick facts

Lead sponsorMovetis
PhasePhase 2
StatusCompleted
Study typeINTERVENTIONAL
Sites1 location across United Kingdom

Drugs / interventions tested

Conditions studied

Sponsor

Movetis — full company profile →

Who can join

18 and older, any sex, with Chronic Intestinal Pseudo-Obstruction. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This study was designed to investigate the clinical safety, tolerability and efficacy of prucalopride in improving the symptoms associated with chronic intestinal pseudo-obstruction (CIP) in subjects with CIP. The study hypothesis was that prucalopride at doses up to 4 mg is safe, well tolerated, efficacious and improves the symptoms associated with CIP.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT00793247.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing