Randomized controlled trial: Comparing a low volume sulfate regimen without bisacodyl, to a polyethylene glycol regimen with bisacodyl at colon preparation for colonoscopy
Phase 4
- Conditions
- Patienten die opgenomen worden voor klinische voorbereiding voor een colonoscopie, ongeacht aandoeningColon adenomasIntestinal polyps
- Registration Number
- NL-OMON45729
- Lead Sponsor
- TweeSteden ziekenhuis
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 200
Inclusion Criteria
All adults (> 18 years of age) seen at the outpatient clinic to be admitted for planned preparation for colonoscopy at the Elisabeth-TweeSteden Hospital in Tilburg were eligible for inclusion in this study.
Exclusion Criteria
Gastro-intestinal obstruction
Bowel perforation
Gastric outlet obstruction
Toxic colitis or toxic megacolon
Hyperemesis
Severe dehydration
Congestive heart failure
Ascites
Severe kidney insufficientie (GFR < 30ml/min/1,73 m2)
Active inflammatory bowel disease (morbus Crohn, ulcerative colitis)
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method