Clinical Trials Directory

Trials / Completed

CompletedNCT04084847

Berberis Vulgaris Consumption and Blood Pressure

Effect of Berberis Vulgaris Consumption on Blood Pressure and Plasma Lipids in Subjects With Cardiovascular Risk Factors

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
78 (actual)
Sponsor
Shahid Beheshti University · Academic / Other
Sex
All
Age
20 Years – 65 Years
Healthy volunteers
Not accepted

Summary

The aim of this study is to investigate the effect of barberry consumption on systolic and diastolic blood pressure, serum lipids, and inflammatory status. The study will involve cases having elevated BP (129/ \< 85) and known hypertensive patients on medical treatment. Seventy people will be randomized into two groups, including intervention (barberry) or placebo groups. Before and after of 8 week intervention, 24-hour ambulatory blood pressure monitoring will be done and fasting venous blood sample will be taken to measure plasma lipids. In addition, 24-hour urine will be collected to measure its sodium content and estimate sodium intake.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTberberis vulgaris=barberry10 grams of barberry powder will be consumed daily for 8 weeks.
DIETARY_SUPPLEMENTPlaceboPlacebo powder

Timeline

Start date
2019-09-18
Primary completion
2020-08-19
Completion
2020-10-21
First posted
2019-09-10
Last updated
2020-10-26

Locations

1 site across 1 country: Iran

Source: ClinicalTrials.gov record NCT04084847. Inclusion in this directory is not an endorsement.