Coronary Heart Disease. Chronic ischemic heart disease, unspecified
Conditions
Interventions
Intervention 1: Intervention group: Four N. Sativa containing capsules (Barij Essence, Kashan, Iran), 500 mg each capsule, daily, for 24 weeks orally. Intervention 2: Control group: Placebo (Barij Ess
Sponsors
Vice chancellor for research, Arak University of Medical Sciences
Eligibility
Sex/Gender
All
Age
45 Years to 85 Years
Inclusion criteria
Inclusion criteria: Patients aged 45-85 years People diagnosed with type 2 diabetes and coronary heart disease
Exclusion criteria
Exclusion criteria: Patients with thyroid disorders. Severe renal insufficiency hepatic failure Those experiencing an acute myocardial infarction within the past 3 months Patients undergoing cardiac surgery within the past 3 months
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Insulin resistance. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Calculation using homeostasis model of assessment insulin resistance formula. | — |
Secondary
| Measure | Time frame |
|---|---|
| Total antioxidant capacity. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Spectrophotometry.;Fasting serum insulin levels. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Elisa kit.;Total cholesterol. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Enzymatic kit.;High-density lipoprotein (HDL) cholesterol. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Enzymatic kit.;Triglycerides. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Enzymatic kit.;High-sensitivity C-reactive protein (hs-CRP). Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Elisa kit.;Nitric oxide. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Spectrophotometry.;Malondialdehyde. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Spectrophotometry.;Glutathione. Timepoint: At the beginning of the study and after 24 weeks of intervention. Method of measurement: Spectrophotometry. | — |
Countries
Iran (Islamic Republic of)
Contacts
Public ContactDr. Fariba Raygan
Kashan University of Medical Sciences
Outcome results
None listed