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Effects of Spirulina consumption on patients with hypertensio

Phase 3
Conditions
Primary Hypertension.
Essential (primary) hypertension
Registration Number
IRCT20200404046940N1
Lead Sponsor
Shiraz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
48
Inclusion Criteria

Systolic blood pressure 130 mm Hg or more
Diastolic blood pressure 80 mm Hg or more
Both of the above
Between the age of 24 and 65 years

Exclusion Criteria

Suffering from cardiovascular, liver, kidney, inflammatory bowel disease, diabetes and thyroid disorders
History of cardiac surgery
Weight loss of more than 5% in the last 3 months
Participate in other studies in the last 6 months
Use any supplements or diets
Pregnancy and lactation
History of inflammation in the past two weeks (including infection, fracture, etc.)

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Blood pressure. Timepoint: Measurement of blood pressure before and 60 days after the intervention. Method of measurement: Digital Arm Sphygmomanometer.;Serum lipid profile. Timepoint: Before and 60 days after the intervention. Method of measurement: By the means of Pars Azmoon Company kit and auto analyzer BT 1500.;Hs-CRP (high-sensitivity C-reactive protein). Timepoint: Before and 60 days after the intervention. Method of measurement: By Enzyme-linked immunosorbent assay (ELISA) kit.;Malondialdehyde. Timepoint: Before and 60 days after the intervention. Method of measurement: Thiobarbituric acid method.
Secondary Outcome Measures
NameTimeMethod
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