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Bioavailability Study of Long Chain Omega-3 Fatty Acids From a Gastric Stable Emulsion

NCT01061554 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 27

Last updated 2010-02-03

No results posted yet for this study

Summary

The purpose of this study is to compare the short term absorption of EPA and DHA from triglycerides (TG) released from normal soft gel capsules and from the new patent pending vehicle providing a gastric stable emulsion.

Conditions

  • Healthy

Interventions

DIETARY_SUPPLEMENT

Omega-3 oils from tri-glycerides

Single-dose administration of approximately 5 grams of omega-3 oils from triglycerides

DIETARY_SUPPLEMENT

Omega-3 oils from marine phospholipids

Single-dose administration of approximately 5 grams of omega-3 oils from marine phospholipids

Sponsors & Collaborators

  • Ayanda AS

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
19 Years
Max Age
29 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2009-03-31
Primary Completion
2009-06-30
Completion
2009-06-30

Countries

  • Norway

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01061554 on ClinicalTrials.gov