Evaluation of the effect of the compound extract of chicory, globe artichoke and milk thistle on non-alcoholic fatty liver
Phase 3
Recruiting
- Conditions
- Fatty liver.Fatty (change of) liver, not elsewhere classified
- Registration Number
- IRCT2017042824198N2
- Lead Sponsor
- Investigator
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 60
Inclusion Criteria
Patients who are willing to participate in the clinical trial; age range 20-70 years; diagnosed with nonalcoholic fatty liver disease; not affected with other disease states such as cardiovascular, digestive and endocrine disorders; not using other herbal medications at least 3 months prior to intervention.
Exclusion criteria: diagnosis of other disease states such as cardiovascular, digestive and endocrine disorders; taking herbal medications, showing allergic responses, unwillingness to participate
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method evel of lipid accumulation in liver. Timepoint: before intervention and 2 months after intervention. Method of measurement: sonography.
- Secondary Outcome Measures
Name Time Method iver enzyme assay. Timepoint: before intervention and after 2 months. Method of measurement: measurement in blood serum.;Fasting blood glucose. Timepoint: before intervention and after 2 months. Method of measurement: measurement in blood serum.;Lipid profile. Timepoint: before intervention and after 2 months. Method of measurement: measurement in blood serum.