Clinical Trials Directory

Trials / Completed

CompletedNCT02575690

Spirulina Supplementation and Cardiovascular Risk in Obese Caucasians With Treated Hypertension

Effect of Spirulina Maxima Supplementation on Cardiovascular Risk in Obese Caucasians With Treated Hypertension:a Randomized Double-blind Placebo-controlled Study

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Poznan University of Medical Sciences · Academic / Other
Sex
All
Age
25 Years – 60 Years
Healthy volunteers
Not accepted

Summary

Potential protective cardiovascular effect of Spirulina maxima supplementation was studied in a double-blind placebo-controlled trial of obese subjects with treated hypertension, each randomized to receive spirulina or a placebo.

Detailed description

Numerous publications have provided evidence of the effect of natural substances-supplements on improving endothelial function, and thus reducing the risk of cardiovascular diseases. Spirulina maxima (Arthrospira maxima) is a species of cyanobacterium, used as food additive because of its high levels of protein and essential nutrients, such as carotenoids, vitamins, and minerals. Various studies point to a possible beneficial effect of spirulina on the concentration of blood serum lipids and fasting glucose,body weight or blood pressure, however, the results of studies pertained to the effects of spirulina in individuals who, at the time of trial, were not taking medications. The aim of the study was to estimate an effect of Spirulina maxima supplementation on cardiovascular risk in obese Caucasians with treated hypertension. The anthropometric parameters, blood pressure, insulin sensitivity, plasma lipid levels, and stress oxidative biomarkers were measured at the baseline and after 3 months of supplementation with spirulina or placebo in the group of obese, hypertensive patients receiving standard antihypertensive treatment.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTSpirulinaIndividuals receive 2 g of spirulina daily, for 3 months.
OTHERPlaceboIndividuals receive a placebo daily, for 3 months.

Timeline

Start date
2013-01-01
Primary completion
2015-05-01
Completion
2016-05-01
First posted
2015-10-15
Last updated
2020-05-05

Source: ClinicalTrials.gov record NCT02575690. Inclusion in this directory is not an endorsement.