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Flaxseed powder and cardiovascular risk factor

Phase 2
Conditions
Condition 1: Hypertention. Condition 2: Dyslipidemia.
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Registration Number
IRCT2016081611763N28
Lead Sponsor
Isfahan University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
80
Inclusion Criteria

Triglyceride concentrations more than 150; Total cholesterol levels more than 200; LDL-C levels more than 130; HDL-C levels less than 40 mg per dl; blood pressure equal to or more than 140/90 mmHg.
Exclusion criteria: Pregnancy ; Breast-feeding; being on a diet during the last three month; renal disease; cancer; Fasting blood sugar more than 110; infection and inflammatory diseases

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Cholestrol. Timepoint: At the first and end of study. Method of measurement: laboratory.;HDL-C. Timepoint: At the first and end of study. Method of measurement: laboratory.;TG. Timepoint: AT THE FIRST AND THE END OF STUDY. Method of measurement: Laboratory measurements.;LDL-C. Timepoint: AT THE FIRST AND THE END OF STUDY. Method of measurement: Laboratory measurements.;Blood pressure. Timepoint: first middle end of the study. Method of measurement: pressure indicator.;Crp. Timepoint: first and end of the study. Method of measurement: Laboratory measurements.;Weight. Timepoint: First,middle and the end of study. Method of measurement: scale.
Secondary Outcome Measures
NameTimeMethod
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