Clinical Trials Directory

Trials / Completed

CompletedNCT01244048

Intervention With n3 LC-PUFA-supplemented Yogurt

Intervention With n3 LC-PUFA-supplemented Yogurt: Effects on Cardiovascular Risk Factors and Inflammatory Biomarkers

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
53 (actual)
Sponsor
University of Jena · Academic / Other
Sex
All
Age
25 Years – 75 Years
Healthy volunteers
Not accepted

Summary

The effective dosage of a n3-LC-PUFA intervention (with n3 LC-PUFA-enriched yoghurt) on the modulation of cardiovascular risk factors and inflammatory biomarkers were determined.

Detailed description

Fifty three mildly hypertriacylglycerolemic subjects (TAG ≥ 150 mg/dL (1.7 mmol/L)) participated on the placebo-controlled, double-blind, parallel designed study. The subjects consumed placebo yoghurt (1), or n3 LC-PUFA-enriched yoghurt (0.8 g n3 LC-PUFA/d (2), 3 g n3 LC-PUFA/d (3)) for 10 weeks. Blood samples were taken at the beginning and at the end of the period. Parameters: * Blood lipids (total cholesterol, HDL, LDL, triacylglycerols) * Fatty acid distribution of plasma lipids (PL) and erythrocyte membranes (EM) * Concentrations of eicosanoids (PGs, HETEs) * Production of ex vivo stimulated cytokines by T cells * SNPs in the CD36 genotype

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTn3 long chain polyunsaturated fatty acidsGroup 1 (placebo) Group 2 (0.8 g n3 LC-PUFA/d in 125 g yoghurt) Group 3 (3 g n3 LC-PUFA/d in 200 g yoghurt)

Timeline

Start date
2009-02-01
Primary completion
2009-04-01
Completion
2009-04-01
First posted
2010-11-19
Last updated
2012-03-07

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT01244048. Inclusion in this directory is not an endorsement.