Randomized controlled trial to compare low dose oral sulfate solution and polyethylene glycol in adults
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0001651
- Lead Sponsor
- Kangbuk Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 210
Inclusion Criteria
1) Adult (aged 19-65) outpatient or screening recipients who undergo colonoscopy for a range of symptoms and treatments.
2) Those who give informed consent to the study
Exclusion Criteria
1) previous colectomy
2) severe constipation, idiopathic colonic pseudoobstruction
3) pregnancy, lactation, and possible pregnancy
4) acute exacerbation of inflammatory bowel disese
5) uncontrolled chronic medical illnesses which hinder trial participation such as major cardiac, renal, metabolic and psychologic disorder
6) acute or chronic acute or chronic azotemia (glomerular filtration rate <30mL/min/1.73m2) or clinical evidence of dehydration
7) allergy or suspicious allergy to polyethylene glycol or oral sulfate solution
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method degree of bowel prepration
- Secondary Outcome Measures
Name Time Method acceptability to bowel preparation agent;satisfaction to bowel preparation agent;Safety (nausea, vomiting, abdominal pain and cramps, bloating, anal irritation and any other adevese events during additional bowel preparation)