Clinical Trials Directory

Trials / Recruiting

RecruitingNCT06975241

Observing Metabolism of EPA With Consideration of Genetics And Sex

Determining Contribution of Sex and Genetics to DHA Synthesis Rates Over 12 Weeks of EPA Supplementation in Healthy Individuals

Status
Recruiting
Phase
Phase 4
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
University of Toronto · Academic / Other
Sex
All
Age
18 Years – 35 Years
Healthy volunteers
Accepted

Summary

The goal of this clinical study is to learn how fast EPA is converted to other molecules, including DHA, with consideration of biological sex and genetics in healthy humans. The main questions it aims to answer are: * How fast is EPA converted to DHA in blood, and is the conversion rate affected by sex and a specific genotype we previously identified? * How do sex and the specific genotypes affect blood DHA levels and other products of DHA in response to dietary EPA? * How fast does dietary EPA replace blood EPA and other omega-3 fatty acids, and is the rate affected by sex and genotype? Participants will be asked to take EPA supplements for 12 weeks and provide a series of venous blood samples over the study duration.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTEPA 2.4g/dayEPA from fish oil will be supplemented to an equal number of males and females for 12 weeks.

Timeline

Start date
2025-07-29
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2025-05-16
Last updated
2026-02-27

Locations

1 site across 1 country: Canada

Source: ClinicalTrials.gov record NCT06975241. Inclusion in this directory is not an endorsement.