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Effect of rosa canina on non alcoholic fatty liver disaese

Not Applicable
Recruiting
Conditions
on alchoholic fatty liver disease.
Fatty (change of) liver, not elsewhere classified
K76.0
Registration Number
IRCT20230903059334N1
Lead Sponsor
Khalkhal university of medical science
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
116
Inclusion Criteria

All people with non-alcoholic fatty liver disease referring to Internist

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
iver enzymes. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Pars azmoon liver enzymes kit.;Lipid profile. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Pars Azmoun Cholesterol Quantification Kit.;Fasting blood sugar. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Glucose Quantification Kit Pars Azman.;Body weight. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Seca scale.
Secondary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Barometer.;Waist circulate. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Measuring tape.;Body fat mass. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Inbody body analyzer.;Body muscle mass. Timepoint: At the beginning of the study and 8 weeks after the start of taking rosa canina supplement. Method of measurement: Inbody body analyzer.
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