Non-alcoholic fatty liver disease. Non-alcoholic fatty liver disease
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: 1. People 18 to 70 years old 2. People with body mass index 25 to 40 3. Diagnosis based on liver fibroscan 4. Have informed consent.
Exclusion criteria
Exclusion criteria: 1. Pregnancy and lactation 2. Hereditary hemochromatosis 3. History of gingival or gastroplasty bypass surgery 4. Use of hepatotoxic drugs such as calcium channel blockers and high doses of synthetic estrogens 5. Patients with hypothyroidism 6. Cushing's syndrome and 7. Kidney failure Kidney stones 8. Cardiovascular disease 9. People with a history of hepatitis B and C 10. Wilson disease
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Alanine Aminotransferase. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kits.;Aspartat transaminase. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kits.;Gamma-glutamyl transpeptidase. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kits.;Hepatic fibrosis. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Fibroscan.;Hepatic steatosis. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Fibroscan. | — |
Secondary
| Measure | Time frame |
|---|---|
| Insulin. Timepoint: Before intervention and 12 weeks after the intervention. Method of measurement: Special kit.;Total antioxidant capacity. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Catalase. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Superoxide dismutase. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;PAB. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;High sensitivity C-reactive protein. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Triglyceride. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Total cholesterol. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;High density lipoprotein cholesterol. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Low density lipoprotein cholesterol. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Special kit.;Homeostatic model assessment of insulin resistance. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Formula.;Insulin sensitivity check index. Timepoint: Before intervention and 12 weeks after intervention. Method of measurement: Formula.;Weight, fat mass, fat free mass, RMR, body mass index and visceral fat. Timepoint: Before intervention and 12 weeks after the intervention. Method of measurement: Omron digital Scale.;Waist,Hip circumference. Timepoint: Before intervention and 12 weeks after the intervention. Method of measurement: Meter.;Diastolic blood pressure. Timepoint: Before intervention and 12 weeks after the intervention. Method of measurement: Sphygmomanometer.;Systolic blood pressure. Timepoint: Before intervention an | — |
Countries
Iran (Islamic Republic of)
Contacts
Yazd University of Medical Sciences