KCT0008442
Not yet recruiting
未知
Comparison of efficacy and safety of 1-L polyethylene glycol plus ascorbic acid for bowel preparation: a randomized multicenter clinical trial
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- The Catholic University of Korea, St. Vincent's Hospital
- Enrollment
- 261
- Status
- Not yet recruiting
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •A patient who is deemed to require an endoscopy due to complaints of digestive symptoms and meets all of the following selection criteria:
- •(1\) Adult males and females between the ages of 19 and 74
- •(2\) Individuals scheduled to undergo upper/lower gastrointestinal endoscopy
- •(3\) Body Mass Index (BMI) \= 30
- •(4\) Voluntarily consents to participate in this clinical trial and signs the consent form.
Exclusion Criteria
- •Individuals who meet any of the following criteria:
- •(1\) History of the following surgeries, medical conditions, or comorbidities:
- •\- Dehydration
- •\-Colorectal resection
- •\- Gastrointestinal obstruction (intestinal obstruction, gastrointestinal obstruction, etc.), perforation, or gastric outlet obstruction (gastroparesis, etc.)
- •\- Inflammatory bowel disease (ulcerative colitis, Crohn's disease, etc.) or toxic megacolon
- •\- Regular or ongoing use of laxatives or stool softeners, or severe constipation requiring physical intervention (e.g. more than 3 bowel movements per week)
- •\- Severe cardiac disease (NYHA class 3,4 heart failure, acute coronary artery disease within 24 weeks prior to screening, clinically significant arrhythmias, hypertrophic obstructive cardiomyopathy, valvular heart disease, aortic disease, and peripheral vascular disease)
- •\- History of cardiac arrest
- •\- Blood coagulation disorders
Outcomes
Primary Outcomes
Not specified
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