Comparison of 4L Polyethylene Glycol and 2L Polyethylene Glycol With Ascorbic Acid in Inactive UC Patients
Not Applicable
Completed
- Conditions
- Ulcerative Colitis
- Interventions
- Registration Number
- NCT01929668
- Lead Sponsor
- Kyungpook National University Hospital
- Brief Summary
The purpose of this study is to compare preference of the patients, efficacy of preparation, and safety between 4 L polyethylene glycol and 2 L of polyethylene glycol with ascorbic acid in patients with inactive ulcerative colitis.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 114
Inclusion Criteria
- age >18 years old
- ulcerative colitis patients without symptoms for at least 1 year
- ulcerative colitis patients who undergo colonoscopy for surveillance
Exclusion Criteria
- subjects who had abdominal surgery
- pregnant or breast feeding
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description polyethylene glycol with ascorbic acid polyethylene glycol 2L polyethylene glycol and ascorbic acid polyethylene glycol polyethylene glycol 4L polyethylene glycol polyethylene glycol with ascorbic acid Ascorbic Acid 2L polyethylene glycol and ascorbic acid
- Primary Outcome Measures
Name Time Method Number of patients who are willing to use the same preparation method for the next colonoscopy. day 1
- Secondary Outcome Measures
Name Time Method Number of patients who have ulcerative colitis symptom aggravation within 30 days after bowel preparation, measured by simple clinical colitis activity index (SCCAI). within 30 days after bowel preparation for colonoscopy
Trial Locations
- Locations (1)
Keimyung University Dongsan Medical Center
🇰🇷Daegu, Korea, Republic of