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

This study is currently recruiting participants.
Verified July 2012 by Benaroya Research Institute
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)