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The effect of algae oil supplements on functional immune response and bioavailability of lipids in blood, a pilot study

The effect of algae oil supplements on functional immune response and bioavailability of lipids in blood, a pilot study - ALG study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON56896
Enrollment
12
Registered
2023-12-13
Start date
2025-06-01
Completion date
Unknown
Last updated
2026-04-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bioavailability of omega-3 fatty acid absorption in blood, immune function, Immune response

Interventions

During each postprandial test day, the subjects receive one of the 3 omega-3-rich supplements (one of 2 types of algae oil supplements or a fish oil supplement control) in capsule form (6 capsules p

Sponsors

Wageningen Universiteit
Lead Sponsor

Eligibility

Age
18 Years to 64 Years

Inclusion criteria

Inclusion criteria: - Apparently healthy men and women; - Age >= 50 years - Body mass index (BMI) >=18.5 and

Exclusion criteria

Exclusion criteria: - Having a disease that may interfere with the outcomes of this study, such as a known metabolic, gastrointestinal, inflammatory or chronic disease (such as anaemia, diabetes, hepatitis, cardiovascular disease), as judged by the medical investigator; - Having a history of medical or surgical events that may significantly affect the study outcome, including: Inflammatory bowel disease, hepatitis, pancreatitis, ulcers, gastrointestinal or rectal bleeding; major gastrointestinal tract surgery such as gastrectomy, gastroenterostomy, or bowel resection; known or suspected gastrointestinal disorders, colon or GI tract cancer; - Use of medication that may interfere with the study outcomes, including gastric acid in-hibitors or laxatives, as judged by the medical supervisor. - Anaemia (Haemoglobin (Hb) values 21 (women) or >28 (men) glasses of alcoholic beverages per week; - Reported weight loss or weight gain of more than 3 kg in the month prior to pre-study screening, or intention to lose weight during the study period; - Reported to follow or having planned a slimming or medically prescribed diet; - Use of drugs; - Current smokers, or stopped smoking in the last 3 months before study start; - Insufficient proficiency in Dutch to understand information brochure and questionnaires; - Participation in any clinical trial including blood sampling and/or administration of sub-stances up to 30 days before test day 1 of this study and during the study period; - Being an employee of the department Food, Health & Consumer Research or Food Quality and Design of Wageningen Food & Biobased Research.

Design outcomes

Primary

MeasureTime frame
The primary study parameter is the functional immune response (ratio pro- and anti-inflammatory markers) measured in isolated PBMCs, collected at 0 hours (baseline), 4 hours, and 8 hours after consumption of the omega-3-rich supplements, and after 1-week exposure to the supplements.

Secondary

MeasureTime frame
The secondary study parameters are the DHA levels in blood and fatty acid levels in plasma and PBMCs, taken before and after the consumption of omega-3-rich supplements.

Countries

Netherlands

Contacts

Public ContactT Hoppenbrouwers

Wageningen Universiteit

tamara.hoppenbrouwers@wur.nl+31653878066

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP) · Data processed: Apr 17, 2026