Non-alcoholic fatty liver disease. Fatty (change of) liver, not elsewhere classified
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Overweight and obese patients (with BMI> 25) With nonalcoholic fatty liver (grade 1, 2) having ultrasound sheet with diagnosis of nonalcoholic fatty liver with radiologist and gastroenterologist approval
Exclusion criteria
Exclusion criteria: Pregnancy and lactation liver transplantation cigarette smoking, alcohol and drugs use medications such as corticosteroids, amiodarone, tamoxifen, pracacillin, methotrexate complete intravenous nutrition heart failure, kidney disease, thyroid failure Hemochromatosis and Wilson disease Having positive test for hepatitis C, B and autoimmune hepatitis alpha-antitrypsin deficiency
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Hepatic enzymes (AST, ALT). Timepoint: Before and after intervention. Method of measurement: Use of enzymatic kits.;Lipid profile (Triglyceride, total cholesterole, LDL, VLDL, HDL). Timepoint: Before and after intervention. Method of measurement: Use of enzymatic kits.;Insulin levels. Timepoint: Before and after intervention. Method of measurement: Use of enzymatic kits.;Liver Echogenicity. Timepoint: Before and after intervention. Method of measurement: Using an ultrasound machine by a radiologist.;The total amount of calorie received. Timepoint: Before and after intervention. Method of measurement: Using a 24-hour food recording questionnaire.;Hs-CRP. Timepoint: Before and after intervention. Method of measurement: Use of enzymatic kits.;Body fat percentage. Timepoint: Before and after intervention. Method of measurement: Using body composition measuring device.;Weight. Timepoint: Before and after intervention. Method of measurement: Using digital scales.;Waist and hip circumference. Timepoint: Before and after intervention. Method of measurement: Use non-elastic tape meters.;Fasting Blood sugar. Timepoint: Before and after intervention. Method of measurement: Use of enzymatic kits.;HOMA-IR. Timepoint: Before and after intervention. Method of measurement: HOMA-IR=BS(mmol/lit)×insulin(microunit/lit)/22.5. | — |
Countries
Iran (Islamic Republic of)
Contacts
Ahvaz University of Medical Sciences