METABOLIC SYNDROME. Endocrine, nutritional and metabolic diseases
Conditions
Interventions
Intervention 1: Intervention group: The intervention group will be consume 4 tablets of 400 miligrams per day garlic. Intervention 2: Control group: The control group will be consume 4 tablets of 400
Sponsors
Bagheiat-allah University of Medical Sciences
Eligibility
Sex/Gender
All
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Age more than 18 y Diagnosis of metabolic syndrome
Exclusion criteria
Exclusion criteria: Kidney disease Cardiovascular disease Type 1 and 2 diabetes Cancers Using blood pressure lower drugs Using blood sugar lower drugs Using anticoagulant drugs Psychiatric disorders Pregnancy and Lactation Allergy to garlic
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| HDL cholesterol. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Enzymatic method, mg/dl. | — |
Secondary
| Measure | Time frame |
|---|---|
| Weight. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Scale, kg.;Body mass index. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Weight(kg)\[height(m)]2 , kg\m2.;Waist Circumference. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: BIA, cm.;Body fat percent. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: BIA.;Triglyceride. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Enzymatic method, mg/dl.;LDL cholesterol. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Enzymatic method, mg/dl.;Total cholesterol. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Enzymatic method, mg/dl.;Systolic blood pressure. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Mercury sphygmomanometer, mmHg.;Diastolic blood pressure. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Mercury sphygmomanometer, mmHg.;Fatty liver index. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Formula.;Quantity of appetite. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: VAS questionnaire.;Intestinal function. Timepoint: at the beginning of the study (before intervention), 6 and 12 weeks after intervention. Method of measurement: Bristol stool questionaire.;Fasting blood sugar. Timepoint: at the beginning of the | — |
Countries
Iran (Islamic Republic of)
Contacts
Public Contactkarim Parastouei
Bagheiat-allah University of Medical Sciences
Outcome results
None listed