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Assessing the impact of escalating fish oil consumption on n-3 polyunsaturated fatty acid (PUFA) content of transport, storage and functional pools

Assessing the impact of escalating fish oil consumption on n-3 polyunsaturated fatty acid (PUFA) content of transport, storage and functional pools: a randomised controlled trial

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN48398526
Enrollment
210
Registered
2006-04-28
Start date
2006-05-01
Completion date
Unknown
Last updated
2019-02-11

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

Conditions

Impact of fish-oil consumption on the fatty acid content of plasma Nutritional, Metabolic, Endocrine Fish oil consumption

Interventions

The five treatment groups are: 1. Control group (n = 42) 2. Capsules equivalent to 1 portion of oily fish per week (containing approximately 1.8 g eicosapentaenoic acid

Sponsors

MRC Human Nutrition Research (UK)
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Men and women, aged 20-80 years with a body mass index (BMI) in the range 18-35 kg/m2 will be recruited to the study.

Exclusion criteria

Exclusion criteria: 1. Known diagnosis of diabetes, cancer, cardiovascular disease or other chronic clinical conditions 2. Untreated hypertension 3. Concomitant prescription of anticoagulants, non-steroidal anti-inflammatory drugs (NSAIDS), aspirin, steroids or immunosuppressants 4. Following a special diet, including vegetarians 5. Allergies or intolerance to fish 6. Consumption of oily fish more than once a month 7. Smokers 8. History of substance abuse or alcoholism 9. Pregnant, 2 kg in past 1 month) 11. Planning to change dietary habits, increase physical activity, change body weight, move away from the study centre locality or take a lengthy vacation during the time of the study

Design outcomes

Primary

MeasureTime frame
The primary outcome is plasma docosahexaenoic acid (DHA) status, expressed as a percentage of total plasma fatty acids. The three primary comparisons (on which sample size has been calculated) are: 1. Differences in plasma DHA status between treatment groups (2 portions versus control group) at 12 months 2. Differences in plasma DHA status between treatment groups (4 portions versus 2 portions group) at 12 months 3. Difference in plasma DHA status between age groups (old versus young) at 12 months

Secondary

MeasureTime frame
Current secondary outcome measures as of 17/01/2019: Secondary comparisons will include gender effects, additional age comparisons and within-group time relationships (i.e. up to 12 months). Additionally, interactions between portions, age, time and gender will be explored. Secondary outcomes will include DHA status of other fatty acid pools (also expressed as a percentage of the total fatty acid profile); EPA status of fatty acid pools, EPA plus DHA status of fatty acid pools, other fatty acids, adipose tissue lipidome, and plasma markers of inflammation and physiological function including lipid mediators (i.e. oxylipins). Previous secondary outcome measures: Secondary comparisons will include gender effects, additional age comparisons and within-group time relationships. Additionally, interactions between portions, age, time and gender will be explored. Secondary outcomes will include DHA status of other fatty acid pools (also expressed as a percentage of the total fatty acid profile).

Countries

United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Mar 8, 2026