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Evaluation of the improvement effects of Vitamin E on liver indexs in pationts with acute hepatitis A

Phase 3
Conditions
Hepatitis A acute.
Acute hepatitis A
Registration Number
IRCT20171205037752N1
Lead Sponsor
Zabol University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
200
Inclusion Criteria

Having Coagulopathy (Encephalopathy
intolerance po
Anti HAV positive

Exclusion Criteria

HAV positive for up to 6 months
Having a abdominal pain
Change the color of the urine
Change the stool color
jaundice
Taking any medication

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Measurement of liver enzyme alanine aminotransferase. Timepoint: Measuring liver enzyme including Alanine aminotransferase before the intervention and two weeks, one, two, three, four and six months after prescribing vitamin E. Method of measurement: In the laboratory by an auto-analyzer.;Measuring the aspartate aminotransferase Liver Enzyme. Timepoint: Measuring liver enzyme including aspartate aminitransferase before the intervention and two weeks, one, two, three, four and six months after prescribing vitamin E. Method of measurement: In the laboratory by an auto-analyzer.
Secondary Outcome Measures
NameTimeMethod
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