hypertension. High blood pressure
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Inclusion criteria: willingness to cooperate in the project and complete a written informed consent, diagnosis of hypertensive patients based on diagnostic criteria and clinical examination by a physician, No pregnant or breastfeeding women, the absence of any autoimmune disorders, cardio - vascular, or renal diseases, lack of nutritional supplements during the past six months Exclusion criteria: diabetes mellitus type 1 or type 2, the history of disease such as myocardial infarction, cardiac dysfunction, cardiac arrhythmia, angina and kidney disease, autoimmune diseases like MS, rheumatism, etc, BMI> 40, factors causing secondary hypertension, supplementation of vitamin, mineral or other nutritional supplements, Alcohol or drug use, Incidence of severe side effects, non-compliance with study protocol
Exclusion criteria
Exclusion criteria:
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| IL6. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Hypertension. Timepoint: At At baseline, weeks after the sixth and twelfth week baseline. Method of measurement: Measured by standard mercury blood pressure measuring device sitting.;IL2. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Hs-CRP. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;TNF-a. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA.;Adiponectin. Timepoint: At baseline, after the sixth week and twelfth week baseline. Method of measurement: ELISA. | — |
Countries
Iran (Islamic Republic of)
Contacts
Shahid Sadughi University of Medical Sciences and Health Services