drugset / Trial / NCT01732692

Evaluation of the Efficacy, Safety and Tolerance of Experimental Morning-only MOVIPREP® Bowel Preparation in Comparison With Split-dose With Nocturnal Pause MOVIPREP® Bowel Preparation

NCT01732692 ↗

Phase 3 Completed 140 enrolled Takeda Norgine · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

To compare colon cleansing quality induced by the 2 different modes of MOVIPREP® intake in 5 colon segments prior to colonoscopy.

Timeline

Start
2012-11
Primary completion
2013-04
Completion
2013-04

Outcome

Met primary endpoint

registry analysis (non-inferiority or equivalence test); MOVIPREP (Morning-only Dose) vs MOVIPREP (Split-dose); p <0.001; Treatment Difference 0.0286; Exact Farrington - Manning NCT01732692 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Moviprep Other / unclassified 2000 ml —

Indications

No indication recorded.