Clinical Trials Directory

Trials / Completed

CompletedNCT01887470

2 Regimens of Lactulose for Colonoscopy Preparation in Adults

A Randomized, Single-blind Pilot Study to Determine the Safety, Efficacy, and Patient Preference of 2 Regimens of Lactulose for Cleansing of the Colon as a Preparation for Colonoscopy in Adults

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
55 (actual)
Sponsor
Cumberland Pharmaceuticals · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

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

Detailed 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.

Conditions

Interventions

TypeNameDescription
DRUGFull dose preparation
DRUGSplit dose preparation

Timeline

Start date
2013-07-01
Primary completion
2013-10-01
Completion
2013-10-01
First posted
2013-06-26
Last updated
2015-06-01
Results posted
2015-06-01

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01887470. Inclusion in this directory is not an endorsement.