Safety, Efficacy, and Patient Preference of Split-Dose Crystalline Lactulose as a Preparation for Colonoscopy in Adults

The recruitment status of this study is unknown because the information has not been verified recently.
Verified July 2012 by Benaroya Research Institute.
Recruitment status was  Recruiting
Sponsor:
Collaborators:
Virginia Mason Hospital/Medical Center
Cumberland Pharmaceuticals
Information provided by (Responsible Party):
Benaroya Research Institute
ClinicalTrials.gov Identifier:
NCT01650870
First received: July 23, 2012
Last updated: July 24, 2012
Last verified: July 2012
No Study Results Posted on ClinicalTrials.gov for this Study
  Study Status: This study is currently recruiting participants.
  Estimated Study Completion Date: September 2012
  Estimated Primary Completion Date: September 2012 (Final data collection date for primary outcome measure)