Type 2 diabetes- Non-alcoholic fatty liver disease. K76.0: Nonalcoholic fatty liver disease [NAFLD]-E11: Type 2 diabetes mellitus
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Subjects are type 2 diabetic women with non-alcoholic fatty liver. They are non-insulin-dependent They use oral medications for treatment (glibenclamide and metformin and sulfonylurease). The maximum blood glycosylated hemoglobin is 11%. The minimum history of diabetes is 1 year and the maximum history of diabetes is 15 years
Exclusion criteria
Exclusion criteria: Patients have retinopathy, nephropathy and severe neuropathy. Have a history of cardiovascular disease and musculoskeletal disorders Severe musculoskeletal problems that restrict physical activity
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Alanine Aminotransferase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Aspartate Aminotransferase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Alkaline phosphatase enzyme. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Glycosylated hemoglobin. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with Pishtaz Teb kit.;HDL Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;LDL Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Cholesterol. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Triglyceride. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with BioSystems kit.;Waist circumference. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Standard tape meter.;Blood Pressure. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: brachial digital blood pressure monitor.;Fasting blood glucose. Timepoint: At the beginning of the study (before the intervention) and two months after the intervention. Method of measurement: Blood test with Bio | — |
Countries
Iran (Islamic Republic of)
Contacts
The University of Tehran