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Study identifier: NCT06361719 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Efficacy of Two HMOs in Chinese Infants

Condition: Healthy Infants  ·  Sponsor: Société des Produits Nestlé (SPN)

PhaseNA
Planned participants262
Who can joinAll sexes, 3 Days to 14 Days
Healthy volunteersYes

About this study

This is a randomized, controlled, double-blind, intervention trial of healthy male and female term infants to evaluate the efficacy of the 2 HMOs on beneficially modulating the gut microbiota, gut maturation, gut barrier integrity, immune response, and other developmental outcomes in healthy Chinese infants. The trial consists of 2 randomized formula-fed groups, and a non-randomized breastfed reference group.

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

Talk to the study team

Qiaoji Li  ·  008613910051543  ·  qiaoji.li@rd.nestle.com

Joyce Li  ·  008615810125435  ·  Joyce.Li@rd.nestle.com

Always discuss trial participation with your own doctor first.

Locations (1)

The International Peace Maternity & Child Health Hospital of China Welfare InstituteShanghai, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT06361719