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Clinical study of 5-ASA concentration in colonic mucosa for patients with ulcerative colitis

Not Applicable
Conditions
lcerative colitis
Registration Number
JPRN-UMIN000031241
Lead Sponsor
Keio University Division of Gastroenterology and Hepatology, Department of Internal Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
60
Inclusion Criteria

Not provided

Exclusion Criteria

Patients who have been 6 weeks or more past relapse diagnosis. Patients with poor medication adherence for 5-ASA drugs Cases using 5-ASA topical therapy (suppository, enema preparation) within 1 week of endoscopy Patient who used steroid formulation (suppository, enema, oral steroid formulation, steroid injectable formulation) or biologic formulation within 2 weeks of endoscopic enrollment. Patients with Crohn's disease or peptic ulcer Patients with history of colorectal surgery Patients with severe renal and liver impairment

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Correlation between 5-ASA concentration in colonic mucosa and colonic endoscopic activity
Secondary Outcome Measures
NameTimeMethod
Correlation between 5-ASA concentration in colonic mucosa and clinical symptoms (Partial UCDAI, DAI, Lichtiger index)
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