Clinical Trials Directory

Trials / Completed

CompletedNCT02039128

KOmparison Study KOmparison Study

A Double-blind, Randomized, Placebo-controlled Study to Assess Changes in the Omega-3 Index in Erythrocytes After Twelve Weeks of Daily Intake of SuperbaTM Krill Oil or Fish Oil

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
240 (actual)
Sponsor
Aker BioMarine Human Ingredients AS · Industry
Sex
All
Age
20 Years – 50 Years
Healthy volunteers
Accepted

Summary

In this double blind, placebo controlled, parallel group study, the relative uptake of 1g/d krill oil in comparison to 1g/d fish oil in healthy female and male adults will be assessed. Primary objective is to determine if a 12 week supplementation with krill oil increases tissue levels in erythrocytes (omega-3 index) significantly more than fish oil after dose adjustments to EPA and DHA levels.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTKrill oil or Fish oil
DIETARY_SUPPLEMENTPlacebo

Timeline

Start date
2014-01-01
Primary completion
2014-07-01
Completion
2014-07-01
First posted
2014-01-17
Last updated
2014-07-29

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT02039128. Inclusion in this directory is not an endorsement.