A randomized clinical study evaluating the efficacy and tolerance of a new, reduced-volume, bowel preparation for colonoscopy ; a comparison between two different regimens
Not Applicable
- Conditions
- general population
- Registration Number
- JPRN-UMIN000014766
- Lead Sponsor
- Department of Endoscopy,Aichi Cancer Center Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 400
Inclusion Criteria
Not provided
Exclusion Criteria
Patients with the following clinical features were excluded: significant cardiac, renal, hepatic, or metabolic co-morbidities, ascites, severe constipation (<2 bowel movement a week), known allergy to PEG-electrolyte solution, history of gastric stapling or bypass procedure, or a history of prior colonic or rectal surgery. Patients were excluded if there was a suspected diagnosis of intestinal obstruction because of advanced colorectal cancer.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Efficacy of bowel preparation
- Secondary Outcome Measures
Name Time Method tolerance, safty, and mucosal visibility