drugset / Trial / NCT01984008

A Study of the Efficacy and Safety of Bowklean and Klean-Prep With Dulcolax for the Bowel Preparation Prior Colonoscopy

NCT01984008

Phase 3 Completed 631 enrolled Universal Integrated Corp.
RandomizedParallel-groupSingle-blindTreatment

Summary

The primary objective of this study is to demonstrate that investigation medication (Bowklean) is not less effective than the active comparator (Klean-Prep with Dulcolax), with regards to the overall quality of bowel preparation in subjects undergoing colonoscopy. An additional objective of this study is to collect subject's response to the acceptability and tolerability about bowel preparation and safety information. After bowel preparation, independent evaluator who is blinded to subject's treatment will evaluate the overall colon cleansing based on Aronchick and Ottawa scale. A total of 600 eligible subjects scheduled to a colonoscopy will be randomly assigned with equal allocation to 1 of 2 treatment groups: "Bowklean" or "Klean-Prep" with Dulcolax. Each subject's participation is expected to be maximally 4 weeks in study duration (up to 3-week screening period followed by one week post colonoscopy).

Timeline

Start
2013-10-23
Primary completion
2014-03-24
Completion
2014-06-17

Drugs

EvaluationDrugModalityDoseRoute
Subject Magnesium Oxide Small molecule
Subject Sodium Picosulfate Unknown
Subject citric acid Unknown

Indications

No indication recorded.