Clinical Trial

Novel Approach to Increase EPA and DHA Levels

Completed Phase 1
View on ClinicalTrials.gov →
Summary
The goal of this intervention trial is to evaluate whether combining meldonium therapy with PUFAs (polyunsaturated fatty acids) supplements containing eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA) changes the plasma (blood component) concentration of EPA and DHA, as well as the acylcarnitine (fatty acid metabolite) profile in healthy volunteers. The main questions it aims to answer are: Does using meldonium together with PUFA supplements increase PUFA (EPA and DHA) concentrations in blood plasma? Does meldonium therapy change change the fatty acid metabolite (acylcarnitine) profile, if used together with PUFA supplements? Researchers compared plasma metabolic parameters in the beginning, middle and end of study period in a group who received only PUFA supplements, with a group which got PUFA supplements at the beginning, but after one month meldonium therapy was added and a group which got meldonium therapy at the beginning, but after one month PUFA supplements were added. Participants: 1. Received detailed information about the study and signed an informed consent form. 2. They were assigned to one of three study groups and received PUFAs and/or meldonium for the duration of the study. 3. Plasma samples were collected at the beginning, middle and end of the study period.
Trial Details
NCT Number NCT07304921
Lead Sponsor Riga Stradins University
Conditions Lipid Metabolism, Omega-3 Polyunsaturated Fatty Acids, Supplementation
Enrollment 48 participants
Start Date 2023-04-06
Primary Completion 2023-06-06 (estimated)
Study Completion 2023-06-06 (estimated)
Updated on ClinicalTrials.gov 2026-07-31