JPRN-UMIN000019310
Completed
未知
Randomized controlled study for concomitant use of 5-aminosalicylic acid suppository with increased dose of oral 5-aminosalicylic acid for moderate to severe patients with ulcerative colitis - Randomized controlled study for concomitant use of 5-ASA suppository with increased dose of oral 5-ASA for moderate to severe patients with ulcerative colitis
Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine0 sites90 target enrollmentNovember 1, 2015
Conditionsulcerative colitis
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- ulcerative colitis
- Sponsor
- Department of Gastroenterology and Hepatology, Osaka University Graduate School of Medicine
- Enrollment
- 90
- Status
- Completed
- Last Updated
- 2 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- Not provided
Exclusion Criteria
- •Coexisting infectious colitis History of administrating more than 3\.0 g of oral 5\-ASA, topical 5\-ASA, oral corticosteroid, tacrolimus before 30 days of enrollment History of receiving anti\-TNF therapy before 60 days of enrollment Regularly administrating NSAIDs before 7 days of enrollment History of administrating topical corticosteroid before 7 days of enrollment Severe renal/liver dysfunction History of allergy for 5\-ASA Concomitant malignant disease With pregnancy or lactation Judged as inadequate for this study by the researchers
Outcomes
Primary Outcomes
Not specified
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