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Study identifier: NCT06943469 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Effect of Partially Hydrolyzed Formula With Synbiotics on Skin Barrier Function

Condition: Atopic Dermatitis (AD)  ·  Sponsor: Société des Produits Nestlé (SPN)

PhaseNA
Planned participants400
Who can joinAll sexes, 1 Day to 14 Days
Healthy volunteersYes

About this study

The main purpose of this study is to assess the efficacy of a partially hydrolyzed formula with synbiotics in halting one of the first steps of the allergic march (atopic dermatitis) in infants at risk of allergy. Other efficacy and safety parameters will be assessed as well.

This description comes directly from the study's public registry record.

Talk to the study team

Amelie Goyer, PhD  ·  +41217858939  ·  Amelie.Goyer1@rd.nestle.com

Always discuss trial participation with your own doctor first.

Locations (23)

AZ Sint-Jan Brugge-Oostende AV - Campus Sint-JanBruges, BelgiumRecruiting
Universitair Ziekenhuis Brussel - KinderziekenhuisBrussels, BelgiumRecruiting
Clinique Ste ElisabethNamur, BelgiumRecruiting
CHU Amiens PicardieAmiens, FranceRecruiting
CHU de CaenCaen, FranceRecruiting
CHU de Grenoble AlpesGrenoble, FranceRecruiting
Hôpital de la Croix RousseLyon, FranceRecruiting
Hôpital Charles NicolleRouen, FranceRecruiting
CHRU de ToursTours, FranceRecruiting
Charite-Universitaetsmedizin Berlin - Campus Virchow-Klinikum (CVK)Berlin, GermanyNot Yet Recruiting
Evangelisches Krankenhaus Düsseldorf - FrauenklinikDüsseldorf, GermanyRecruiting
Klinik für Kinder- und Jugendmedizin, Universitätsklinikum FrankfurtFrankfurt, GermanyRecruiting

+ 11 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT06943469