Type 2 diabetes Mellitus. Type 2 diabetes mellitus without complications
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Overweight and obese adults with BMI between 25 to 40 Suffering from Type 2 diabetes mellitus using oral medications Suffering from hyperlipidemia using oral medications Aged 20 to 60 years Willingness of participating Not using slimming medication for 3 months prior to the study Absence of thyroid, kidney, liver or cardiovascular diseases Absence of metabolic (except type 2 diabetes), endocrine or congenital disorders
Exclusion criteria
Exclusion criteria: Undergoing slimming, gastric bypass surgery Participating in other clinical trials Being pregnant or in lactation period
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fasting blood glucose. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method. | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Scale - kg.;Triglyceride. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;Serum total cholesterol. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;Low density lipoprotein. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;High-density lipoprotein. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;MDA. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;ALT. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method.;AST. Timepoint: At the beginning of the study (before the intervention) and 3 months after the start of intervention. Method of measurement: Standard enzymatic method. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shiraz University of Medical Sciences