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Efficacy and Safety of Bisacodyl and Lactulose as a Preparation for Colonoscopy

Colonoscopy Preparation Clinical Trial

Official title:
An Observer-blinded, Dose-finding Study to Investigate the Safety, Efficacy, and Patient Preference of Lactulose for Oral Solution With Bisacodyl for Cleansing of the Colon as a Preparation for Colonoscopy in Adults

Clinical Trial Summary

The purpose of the study is to evaluate the efficacy and safety of bisacodyl combined with escalating doses of lactulose to be used as a preparation for colonoscopy.

Clinical Trial Description

n/a

Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02123017
Study type Interventional
Source Cumberland Pharmaceuticals
Contact
Status Completed
Phase Phase 2
Start date April 2014
Completion date August 2014
View Details
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