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CompletedNCT02427373

A Parallel Bioavailability Study of Fish Oil-Ethyl Ester Versus Fish Oil-Triglyceride Versus Krill Oil

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
66 (actual)
Sponsor
dsm-firmenich Switzerland AG · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Accepted

Summary

A multiple-dose, double-blind, randomized, four-week, three-treatment, parallel study in which 66 healthy adult subjects will receive 6 capsules/d, administered as a dose of 1.3 g/d eicosapentaenoic acid (EPA)+docosahexaenoic acid (DHA) in fish oil ethyl ester (EE), or fish oil triglyceride (TG) or krill oil for a total of 4 weeks. The objective of the study is to compare the oral bioavailability of EPA+DHA in total plasma across the three formulations at the end of the 4 week study.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTfish oil ethyl ester
DIETARY_SUPPLEMENTfish oil triglyceride
DIETARY_SUPPLEMENTkrill oil

Timeline

Start date
2014-06-01
Primary completion
2014-08-01
Completion
2014-12-01
First posted
2015-04-28
Last updated
2015-04-28

Source: ClinicalTrials.gov record NCT02427373. Inclusion in this directory is not an endorsement.

A Parallel Bioavailability Study of Fish Oil-Ethyl Ester Versus Fish Oil-Triglyceride Versus Krill Oil (NCT02427373) · Clinical Trials Directory