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Effect of n-3 Polyunsaturated Fatty Acids Supplementation on Human Milk Composition of Lactating Women

Not Applicable
Completed
Conditions
Nursing Women
Interventions
Dietary Supplement: nutritional intervention
Registration Number
NCT01288313
Lead Sponsor
University Hospital, Bordeaux
Brief Summary

We propose to measure the LCPUFA human milk (linolenic acid, linoleic acid, docosahexaenoic acid, arachidonic acid) according to fatty acids nature and quantities consumed by lactating women

Detailed Description

n-3 and n-6 long chain polyunsaturated fatty acids (LCPUFA) are essential particularly to neurodevelopment of newborn infants. Many variations in essential PUFA and LCPUFA content of human milk are observed according to countries and dietary habits of the mothers.

Maternal diet supplementation of LCPUFA of lactating women may increase LCPUFA human milk according to consensus recommendations.

This clinical trial is performed to evaluate the effect of different of consumption of n-3 fatty acids (linolenic acid) in different forms (oils or margarine) in the human milk composition.

Each diet will last 30 days. During the first period of 15 days, the mothers will receive mediterranean diet based on olive oil. Then, lactating women will be randomised into four groups : one group will receive olive oil (standard group), one group supplemented in rapeseed oil, one group with n-3 margarine and one group with diet associating rapeseed oil and n-3 margarine.Human milk will be collected during the first breastfeeding of the day (10 ml) at three times : Days 0 corresponding to the usual diet , at day 15 after the Mediterranean diet and at day 30, after the study diet.

Recruitment & Eligibility

Status
COMPLETED
Sex
Female
Target Recruitment
82
Inclusion Criteria
  • Lactating women more than 1 month and less than 4 month with neonate whom term is between 37 and 42 gestational age
  • Women who agree to consume fatty fish two times per week
  • Free consent
Exclusion Criteria
  • Women with multiple infants
  • Chronic treatments more than 8 days
  • Women with treatment during supplementation period
  • Women with maternal pathology not compatible with breastfeed

Study & Design

Study Type
INTERVENTIONAL
Study Design
FACTORIAL
Arm && Interventions
GroupInterventionDescription
n-3 margarine and rapeseed oilnutritional intervention-
n-3 margarinenutritional intervention-
Olive oilnutritional intervention-
rapeseed oilnutritional intervention-
Primary Outcome Measures
NameTimeMethod
Acide linolenic 18 :3 n-3 analysis measured at day 30, compared to day 1530 days
Secondary Outcome Measures
NameTimeMethod
Analysis of linolenic acid and linoleic acid ratio30 days
Analysis of arachidonic acid, docosahexanoic acid and their ratio30 days
Comparison of fatty acid composition of human milk before and after supplementation30 days
Analysis of trans fatty acids according diets30 days

Trial Locations

Locations (4)

Lactarium Institut de Puériculture de Paris et de Périnatalogie

🇫🇷

Paris, France

Lactarium CHU Montpellier Pédiatrie 2

🇫🇷

Montpellier, France

Lactarium Hôpital Pellegrin Enfants CHU Bordeaux

🇫🇷

Bordeaux, France

Lactarium CHU La Croix Rousse Lyon Néonatologie et Réanimation Néonatale

🇫🇷

Lyon, France

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