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BI and chromoendoscopy surveillance for longstanding ulcerative colitis patients, prospective study

Not Applicable
Conditions
lcerative Colitis
Registration Number
JPRN-UMIN000013527
Lead Sponsor
avigator Study Group
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
All
Target Recruitment
260
Inclusion Criteria

Not provided

Exclusion Criteria

1) The patient who was performed total or subtotal colectomy. 2) The patients who is not able to examined with surveillance colonoscopy by using EVIS LUCERA ELITE CF-HQ290I (Olympus Co., Japan). 3) The patient who is judged as inadequate by primary investigator or physician.

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The detection rate of panchromoendoscopy group and NBI group
Secondary Outcome Measures
NameTimeMethod
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