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To Evaluate the Health Effect of Particular Fatty Acids Profiles From Eggs

To Evaluate the Health Effect of Particular Fatty Acids Profiles From Eggs

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05413954
Acronym
Omegasnack
Enrollment
24
Registered
2022-06-10
Start date
2020-10-22
Completion date
2021-06-11
Last updated
2022-06-10

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

Conditions

Abdominal Obesity

Brief summary

In a previous study, 24 volunteers consumed two conventional eggs or two eggs naturally enriched with omega 3, 5 and 7 every day for 3 months. It was shown that these eggs were well tolerated and that the omega enrichment led to a reduction in waist circumference of 3 cm in 3 months. The objective of Omegasnack study was therefore to go further in the evaluation of these effects on waist circumference; 1) confirm the effects of these eggs on waist circumference when included in a snack, 2) determine whether this reduction in waist circumference is linked to a reduction in muscle and/or fat mass (subcutaneous and/or visceral) and 3) evaluate whether these effects are associated with a modification in the accumulation of ectopic fat in the muscle and/or liver.

Interventions

OTHERControl

Control group ate snacks composed of dried vegetables, one classical egg yolk and 2.3g of sunflower oil during 10 weeks

OTHERTest

Tes group ate snacks composed of dried vegetables, one test egg yolk naturally enriched in rumenic acid, docosahexaenoic acid and punicic acid, 0.34g of pomegranate seed oil and 2.26g of olive oil during 10 weeks

Sponsors

Université Catholique de Louvain
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
Yes

Inclusion criteria

* Woman or man, aged of 18 to 75 years; * Abdominal obesity: waist circumference for men \> 94cm and \> 80cm for women; * Body mass index ≥ 25kg/m2 and ≤30kg/m2; * For women: use of effective contraception; * Provision of signed and dated informed consent form; * Stated willingness to comply with all study procedures and availability for the duration of the study; * French speaker.

Exclusion criteria

* Uncontrolled systolic blood pressure \> 160/100 mmHg; * For premenopausal women: pregnant women or women planning to get pregnant within 3 months or lactating women; * For menopausal women: less than 6 months of menopause; * For Perimenopausal women: presenting symptoms; * Type II diabetes (controlled or uncontrolled), Type I diabetes; * Medical history or actual cardiovascular disease (myocardial infarction, angina, transient ischemic attack, lower limb arteriopathy); * Medical history or actual severe psychiatric, hepatic, pancreatic, kidney, pulmonary or gastrointestinal problem * Thyroid disorder; * Cancer \< 3 years before the screening visit; * Smokers or who have stopped smoking within the last 6 months before the screening visit; * Subject presenting allergy or food intolerance to eggs; * Subjects who are not able to understand and follow study procedures; * Drug addiction problem (regular consumption); * Recent change of body weight \> 7% (\< 2 months before the inclusion); * Within 1 month before the screening visit, change in the chronic (\> 7 days in a row) intake or dosage of drug(s) or product(s) modifying the glucose and/or lipid metabolism; * Current or recent (\< 2 months before the screening visit) intake of dietary supplements rich in n-3 polyunsaturated fatty acid (including tablets, pills, capsules, enriched-oils); * Vegan diet; * Consumption of fish \> 3 times per week; * Women who drink more than 2 glasses of alcohol per day (\> 20 g of alcohol per day or \> 140g/week) or men who drink more than 3 glasses of alcohol per day (\> 30 g of alcohol per day or more than 210g/week); * LDL \> 159 mg/dl or Total cholesterol \> 239 mg/dl; * Subjects having participated to another clinical trial \< 1 month before the screening test visit.

Design outcomes

Primary

MeasureTime frame
Change from baseline of waist circumference at 10 weeksBaseline, 10 weeks
Change from baseline of waist circumference at 5 weeksBaseline, 5 weeks

Secondary

MeasureTime frameDescription
Plasma fatty acid patternBaseline, 5 weeks, 10 weeks
Plasma triglycerideBaseline, 5 weeks, 10 weeks
Plasma LDL cholesterolBaseline, 5 weeks, 10 weeks
Plasma total cholesterolBaseline, 5 weeks, 10 weeks
Plasma HDL cholesterolBaseline, 5 weeks, 10 weeks
Plasma non-HDL cholesterolBaseline, 5 weeks, 10 weeks
GlycemiaBaseline, 5 weeks, 10 weeks
InsulinemiaBaseline, 5 weeks, 10 weeks
HOMA (Homeostatic Model Assessment for Insulin Resistance)Baseline, 5 weeks, 10 weeks
QUICKIBaseline, 5 weeks, 10 weeks
Body weightBaseline, 5 weeks, 10 weeks
SatietyBaseline, 5 weeks, 10 weeksVisual analog scale (between 0 = no satiety to 100 = complete satiety)
Impedancemeter fat massBaseline, 5 weeks, 10 weeks
Hip circumferenceBaseline, 5 weeks, 10 weeks
CRP (c-reactive protein)Baseline,10 weeks
Oxidized LDLBaseline,10 weeks
Endothelial statusBaseline,10 weeksHbNO (hemoglobin-NO adduct)
Liver stiffnessBaseline,10 weeksTransient elastography
Liver steatosisBaseline,10 weeksControlled attenuation parameter (CAP)
Subcutaneous fat area evaluated by computed tomography (CT) scanBaseline,10 weeks
Visceral fat area evaluated by computed tomography (CT) scanBaseline,10 weeks
Skeletal muscle index (total skeletal muscle area normalized for stature) evaluated by computed tomography (CT) scanBaseline,10 weeks
Muscular radiation attenuation (fat accumulation in muscle) evaluated by computed tomography (CT) scanBaseline,10 weeks
Impedancemeter lean massBaseline, 5 weeks, 10 weeks
Red blood cells fatty acid patternBaseline, 5 weeks, 10 weeks

Countries

Belgium

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026