Evaluation of pre-treatment of additional water-supplementation in order to induce the sufficient effects of Moviprep
Not Applicable
- Conditions
- The purpose of this study is to induce the sufficient effects of Moviprep by comparison with or wothout water-supplementation
- Registration Number
- JPRN-UMIN000015163
- Lead Sponsor
- Saitama Medical Center, Saitama Medical University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 0
Inclusion Criteria
Not provided
Exclusion Criteria
Patients who have or who are suspected to have gastrointestinal obstruction. Patients who has intestinal perforation. Patients who has delayed outlet of stomach. Patients who has toxic megacolon. Patients who allergy of Moviprep. Patients who are not suitable to this study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method cleansing effects of large bowel for the colonoscop including of total laxative volume, preparation time, endoscopic evaluation
- Secondary Outcome Measures
Name Time Method rinary osmotic pressure and specific gravity, patients' tolerability and safety