Effect of Fish Oil on Atopic Dermatitis
Official title: A Randomized, Double-blinded Nutritional Study to Determine the Effect of a Concentrated Cetoleic Acid Fish Oil on Atopic Dermatitis
Run by Møreforsking AS · NCT06194045 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing if a fish oil supplement can help people with mild to moderate eczema improve their skin condition over six months.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 80 Years |
| Sex | All |
| Enrollment | 60 (estimated) |
| Sponsor | Møreforsking AS Academic / other |
| Locations | 1 site (Ålesund, Møre Og Romsdal) |
| Trial ID | NCT06194045 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates are men and women aged 18-80 with a diagnosis of active mild to moderate atopic dermatitis.
✕Probably not a fit
Patients with known allergies to fish products or those with other skin diseases may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study investigates the impact of cetoleic acid, a long-chain monounsaturated fatty acid found in fish oil, on individuals with mild to moderate atopic dermatitis. Participants will be randomly assigned to receive either cetoleic-rich fish oil or a placebo for a duration of six months. The study aims to assess changes in skin condition and inflammation levels before, during, and after the intervention. By examining the lipid composition and microbiome changes, the research seeks to understand the potential benefits of cetoleic acid in managing atopic dermatitis.
Why it matters
Potential benefit: If successful, this study could provide a new dietary approach to effectively manage and alleviate symptoms of atopic dermatitis.
How similar studies have gone: Previous studies have indicated an anti-inflammatory effect of cetoleic acid, suggesting potential success for this approach.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Women and men 18-80 years of age. * Diagnosed with active mild to moderate atopic dermatitis with an EASI of 1.1- 21.0. * Willing to refrain from oil supplements (omega-3, borage, evening primrose, etc.) for 1 month before study begin (washout) and during the study * Willing to take the study supplement for 6 months Exclusion Criteria: * Known allergy to fish products * Subjects known to be pregnant or breast feeding * Subjects perceiving systemically administered medication for AD (other than topical) * Subjects with auto-immune diseases (except asthma and seasonal/perennial rhinitis) * Subjects with a diagnosis of other skin diseases
Where it's running
-
Helse Møre og Romsdal HF
Ålesund, Møre Og Romsdal, Norway Recruiting
Study contacts
- Principal investigator: Dag Arne Lihaug Hoff — Helse Møre og Romsdal HF
- Study coordinator: Lisa Kolden Midtbø, PhD
- Email: lisa.kolden.midtbo@moreforsking.no
- Phone: +47 70 11 16 00
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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Roflumilast Cream 0.3% for moderate to severe atopic dermatitis in children, adolescents, and adults
A cream called roflumilast 0.3% is tested once daily to see if it helps people with moderate to severe atopic dermatitis, compared to a non-medicated cream, across ages 6 and up.
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This study tests whether the Replior ScratchSense ring can accurately detect and measure nighttime scratching in adults with itchy skin conditions.
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ADBest TREAT Registry for adults with atopic dermatitis
A registry in Germany is collecting real-world data from adults with atopic dermatitis to see how treatments are used and how the disease affects quality of life.
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How lebrikizumab affects the skin microbiome and mycobiome in adults with atopic dermatitis
This study looks at whether lebrikizumab changes the skin bacteria, fungi, and specifically Staphylococcus species, in adults with moderate-to-severe atopic dermatitis.
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QX-4533 safety study in healthy volunteers and people with moderate-to-severe atopic dermatitis
This study tests the safety and tolerability of QX-4533, given as a pill, in healthy adults and in patients with moderate-to-severe atopic dermatitis to see how the drug behaves in the body and what side effects may occur.
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Tilrekimig for moderate-to-severe eczema in teens and adults
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.