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Impact of phlebotomy on steatohepatitis

Not Applicable
Conditions
onalcoholic steatohepatitis (NASH).
Other specified inflammatory liver diseases
Registration Number
IRCT20161205031252N4
Lead Sponsor
Ghoum University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
40
Inclusion Criteria

age between 18-65 years
proven steatohepatitis with sonography or fibro scan
Hb more than 13 in men and more than 12 in women
Informed consent

Exclusion Criteria

any other liver disease
history of alcohol use (more than 10gr daily for women and more than 20gr daily for men)
pregnant and lactating women
women in childbearing age with no reliable Contraception method
weight under 50kg
uncontrolled underlying disease
contraindication of vitamin E use

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver fibrosis. Timepoint: before intervention and after 6 month. Method of measurement: fibroscan.;Liver function. Timepoint: before intervention and after 6 month. Method of measurement: Blood samples laboratory study.
Secondary Outcome Measures
NameTimeMethod
Ferritin level. Timepoint: at the begining of study and 6 months later. Method of measurement: Laboratory blood level measurement.
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