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Effect of herbal extracts on fatty liver disease

Phase 2
Conditions
fatty liver disease.
Fatty (change of) liver, not elsewhere classified
Registration Number
IRCT2017082935963N1
Lead Sponsor
Vice Chancellor for research of Sabzevar University of Medicine Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
82
Inclusion Criteria

AST, ALT more than 1.5 equivalents of normal range plus sonographic confirmation; from 20 to 60 years old
Exclusion criteria :
alcoholic drinks user( now or in past); being athlete; hospitalized; Acute or chronic disease before or at the time of intervention that can affects liver function tests; Taking drugs before or at the time of intervention that could affects liver function tests; Pregnancy or breastfeeding; Younger than 20 or older than 60 years old

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Aminotransferases. Timepoint: 1-3 days before intervention and 40 days after intervention. Method of measurement: U/L.
Secondary Outcome Measures
NameTimeMethod
Cholestrol. Timepoint: 1-3 days before intervention and 40 days after the intervention. Method of measurement: Mg/dl.;Triglyceride. Timepoint: 1-3 days before intervention and 40 days after the intervention. Method of measurement: Mg/dl.;Fasting blood sugar. Timepoint: 1-3 days before intervention and 40 days after the intervention. Method of measurement: Mg/dl.
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