A Multicenter Clinical Trial To Assess The Efficacy Of Antenatal Maternal Supplementation With GOS/Inulin Prebiotics On Atopic Dermatitis Prevalence In High-Risk One-Year-Old Children.
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Dermatitis, Atopic
- Sponsor
- Nantes University Hospital
- Enrollment
- 376
- Locations
- 5
- Primary Endpoint
- atopic dermatitis prevalence at M12
- Last Updated
- 4 years ago
Overview
Brief Summary
Allergies are increasing worldwide affecting 30-40% of the population. Among this, Atopic Dermatitis (AD) is the earliest and the most common manifestation of allergic diseases (prevalence 20%). Recent studies have shown that allergies were associated with a disruption of the gut microbial 'balance' suggesting that the use of nutritional intervention very early in life may restore an optimal pattern of microflora aiming at improving the host's health. So far, most human intervention studies have mainly focused on improving postnatal infant colonization. Our study will test the hypothesis that a maternal antenatal prebiotics (GOS/inulin) supplementation may be superior to placebo for AD prevention in high-risk children.
Detailed Description
Study design : Inclusion visit at 20 weeks of gestation : * randomization * start of supplementation (GOS/inulin or placebo) Phone call at 24 weeks of gestation : * checking tolerance * checking observance 32 weeks of gestation visit : * replenishment of prebiotics * collect of AE Day 1 : assessment of the Transepidermal Waterlos evaluated by a TEWAMETER Delivery/per partum Visit At M3 : The national recommendations for the dietary diversification of the child will be transmitted to the patients At M6 : evaluation of AD prevalence by parents At M12 : Pediatric dermatology consultation * clinical exam of child * the SCORAD * the POEM questionnaire * prevalence of AD * skin prick tests * FDQLI score * assessment of the Transepidermal Waterlos evaluated by a TEWAMETER * prevalence of food allergies
Investigators
Eligibility Criteria
Inclusion Criteria
- •pregnant women with an eutocic pregnancy before 20 weeks of gestation
- •women with personal history of atopy diagnosed by a healthcare Professional
- •Women accepting a complete avoidance of dietary supplements containing prebiotics or probiotics during study supplementation
- •women accepting dermato-pediatric follow-up during the first year of life of the new-born (Phone calls at 24 weeks of gestation and 6 months of child and a consultation at 12 months of age)
- •non Tobacco user women
- •women over 18 years
- •women without history of severe gestational diabetes
Exclusion Criteria
- •women not giving up on intake of dietary supplements containing prebiotics or probiotics during study supplementation
- •women refusing dermato-pediatric follow-up during the first year of the newborn
- •ongoing allergy and/or intolerance to cow's milk proteins
- •term \>21 weeks of gestation
Outcomes
Primary Outcomes
atopic dermatitis prevalence at M12
Time Frame: at 12 months of age
prevalence will be evaluated according to UK party working group criteria
Secondary Outcomes
- atopic dermatitis severity(at 12 months of age)
- food allergies prevalence at M12(at 12 months of age)
- sensitization with the major allergens(at 12 months of age)
- Quality of life of the child and his/her family(at 12 months of age)
- atopic dermatitis prevalence at M6(at 6 months of age)
- Tolerance of the prebiotics in mothers(from inclusion to delivery)
- assessment of the Transepidermal Waterlos(at J1 and at 12 months of age)