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Active Not RecruitingNCT06629103

A Study in Healthy Subjects to Compare the Bioavailability of EPA + DHA

A Randomized, Double-blind Placebo-controlled Study in Healthy Subjects to Compare the Bioavailability of EPA + DHA From Two Microalgal Sources to One Fish Source

Status
Active Not Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
120 (estimated)
Sponsor
RDC Clinical Pty Ltd · Industry
Sex
All
Age
18 Years – 64 Years
Healthy volunteers
Accepted

Summary

This is a randomised, double-blind, parallel, placebo-controlled study in healthy subjects to compare the absorption of two microalgal formulations, to a fish oil and a placebo.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTlife's Omega 1035DSA natural triglyceride derived from microalgae with minimum 365 mg DHA, minimum 100 mg EPA, and minimum 520 mg/g DHA + EPA. Participants receive 600mg/d of omega-3 fatty acids from the microalgal oil.
DIETARY_SUPPLEMENTFish OilCommercially available fish oil product MEG-3 1812 TG with a minimum 100 mg DHA/capsule, minimum 160 mg EPA/capsule, and minimum 300 mg/g DHA+EPA. Participants receive 600mg/d of omega-3 fatty acids from the fish oil.
OTHERPlaceboThe placebo capsules will be a mixture of corn and soybean oils. Participants receive 600mg/d of omega-3 fatty acids from the corn/soy placebo.
DIETARY_SUPPLEMENTlife's Omega O3020DSA natural triglyceride derived from microalgae with minimum 210 mg DHA, minimum 300 mg EPA, and minimum 510 mg/g DHA + EPA. Participants receive 600mg/d of omega-3 fatty acids from the microalgal oil.

Timeline

Start date
2025-08-06
Primary completion
2026-12-01
Completion
2026-12-01
First posted
2024-10-08
Last updated
2025-11-18

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT06629103. Inclusion in this directory is not an endorsement.