Non alcoholic fatty liver. Fatty (change of) liver, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: All obese patients with grade 2 or higher of non-alcoholic fatty liver The increase in liver enzymes (ALT) is more than 1.5 times normal
Exclusion criteria
Exclusion criteria: Chronic Pulmonary Disease?other liver diseases,heart attack and any chronic kidney and peptic diseases. The history of drinking alcohol. Smoking and drug use. Use of diuretics and Nonsteroidal anti-inflammatory drugs (NASID), estrogen, tamoxifen, corticosteroids and hypoglycemic agents within 3 weeks before the start of the study. Evidence of infection with viral hepatitis. Pregnancy and lactation or use contraceptive pills. Having a particular diet in the last 3 months. Having a history of weight loss surgery in the last year. Average raisin daily intake of more than half a serving in a day.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Degree of hepatic steatosis. Timepoint: At baseline and end of the study. Method of measurement: Ultrasound sonography assessment. | — |
Secondary
| Measure | Time frame |
|---|---|
| Liver enzymes. Timepoint: At baseline and end of the study. Method of measurement: Using biochemical method and Pars azmoon Company's Kit.;IL-6. Timepoint: At baseline and end of the study. Method of measurement: Using Enzyme-Linked Immunosorbent Assay (ELISA).;Malondialdehyde. Timepoint: At baseline and end of the study. Method of measurement: Thiobarbituric acid colorimetric method (TBARS).;Total antioxidant capacity. Timepoint: At baseline and end of the study. Method of measurement: Using the Ferric Reducing Ability of Plasma Method and based on colorimetric method.;Insulin. Timepoint: At baseline and end of the study. Method of measurement: Using Enzyme-Linked Immunosorbent Assay (ELISA).;Fasting Blood Glucose. Timepoint: At baseline and end of the study. Method of measurement: Using Enzymatic method (Glucose Oxidase) and Pars azmoon Company's kit.;Lipid profile. Timepoint: At baseline and end of the study. Method of measurement: Using Enzymatic method and Pars azmoon Company's kit.;Weight. Timepoint: At baseline and end of the study. Method of measurement: Measure with a scales. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ahvaz University of Medical Sciences