Clinical Trial

Exploring Sustainable Alternatives to Marine Oils With Echium and Ahiflower Oils

Active, Not Recruiting
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Record status
This record was last updated December 17, 2025 (before its estimated March 5, 2026 completion). Its status may not reflect the trial's current state.
Summary
This randomized, single-blind, crossover clinical trial aims to evaluate Echium oil and Ahiflower® oil as sustainable, plant-based alternatives to marine oils for omega-3 supplementation. Although fish oil is the primary dietary source of eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), its use as a dietary supplementation presents several drawbacks, including high cost, potential contamination, limited global supply, and sustainability concerns. Echium and Ahiflower oils are naturally rich in stearidonic acid (SDA), a metabolic intermediate that bypasses the rate-limiting Δ6-desaturase step in the omega-3 pathway, potentially enhancing the conversion to EPA. Fifteen participants will undergo three 8-week intervention phases-Echium oil (15 g/day), Ahiflower oil (15 g/day), or EPA capsules (2.34 g/day)-separated by four-week washout periods. Blood samples will be collected before and after each phase to measure fatty acid profiles in plasma, plasma fractions, and erythrocytes using GC-MS. Anthropometric and biochemical parameters will also be assessed. The study seeks to determine whether SDA-rich plant oils can effectively increase EPA levels in humans and potentially reduce the reliance on marine oils for cardiovascular health benefits.
Trial Details
NCT Number NCT07289919
Lead Sponsor University of Sao Paulo
Conditions Cardiovascular (CV) Risk, Atheroscleroses, Inflamation, Omega 3 Fatty Acids, Supplement
Enrollment 15 participants
Start Date 2025-05-26
Primary Completion 2026-03-05 (estimated)
Study Completion 2026-12-31 (estimated)
Updated on ClinicalTrials.gov 2025-12-17