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
| Type | Name | Description |
|---|---|---|
| DRUG | Full dose preparation | |
| DRUG | Split 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.