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atural history of Lower Gastrointestinal Bleeding of unknown origi

Not Applicable
Conditions
hematochezia
Registration Number
JPRN-UMIN000045955
Lead Sponsor
Dokkyo Medical University Hospital Department of Gastroenterology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
159
Inclusion Criteria

Not provided

Exclusion Criteria

Exclusion criteria 1. those in whom hematochezia was not observed after the hospital visit 2. those who received endoscopic treatment within 1 month before the visit 3. those for whom observation up to the terminal ileum could not be done using colonoscopy 4. those for whom the cause of hematochezia was identified during the first colonoscopy 5. those who had no follow-up visit after hospital discharge (follow-up period 0 day) 6. those who had a past history of hematochezia

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The rebleeding rate in hematochezia patients with an unidentified bleeding source
Secondary Outcome Measures
NameTimeMethod
The period until rebleeding, total number of rebleeding episodes, the source of bleeding and the identification rate in rebleeding, the bleeding-related death rate, and rebleeding risk factors
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