2 Regimens of Lactulose for Colonoscopy Preparation in Adults

Status Completed

Clinical Trial Summary

The purpose of the study is to determine the efficacy of 2 regimens of lactulose as a preparation for colonoscopy.

Clinical Trial Description

A full-dose regimen of lactulose for oral solution, where all dosing is completed the evening prior to the colonoscopy procedure, will be studied and compared to a split-dose regimen, where three doses are taken on the prior evening, and one dose is taken the morning of the procedure. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Colonoscopy Preparation

Clinical Trial Details

NCT number	NCT01887470
Study type	Interventional
Source	Cumberland Pharmaceuticals
Contact
Status	Completed
Phase	Phase 2
Start date	July 2013
Completion date	October 2013

View Details

See also
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