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Study to Evaluate the Effects of a Formula on the Gut Health of Healthy Chinese Infants and Young Children

A Prospective, Multicentre Before and After Study to Evaluate the Effects of a Formula With Prebiotics and Milk Fat, on the Gut Health of Chinese Infants and Young Children

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04864665
Enrollment
455
Registered
2021-04-29
Start date
2021-05-12
Completion date
2023-10-12
Last updated
2023-10-31

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

Conditions

Healthy Children

Keywords

Prebiotics, Gut microbiota, Formula

Brief summary

The infant gut microbiota, a major driver of the maturation of the immune system, is formed through the successive establishment and development during infancy and early childhood. It can inhibit the growth of pathogenic bacteria, prevent the occurrence of diseases and improve the child's quality of life. It is therefore important to regulate the microbiota balance in infants and young children. This objective of this post-launch study is to evaluate the effects of a formula with prebiotics and milk fat on the gut microbiota and stool characteristics of healthy Chinese infants and young children. The duration of the study for each participant is 32 days and includes 3 study visits.

Interventions

DIETARY_SUPPLEMENTa formula with prebiotics and milk fat

Provided in a formula added with prebiotics and milk fat for 1 month

Sponsors

Nutricia Early Life Nutrition (Shanghai) Co., Ltd
CollaboratorUNKNOWN
Danone Nutricia
Lead SponsorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
OTHER
Masking
NONE

Intervention model description

interventional with breastfed reference group

Eligibility

Sex/Gender
ALL
Age
No minimum to 2 Years
Healthy volunteers
Yes

Inclusion criteria

* The gestational age was 37-42 weeks at birth; * Birth weight ≥2,500 g and ≤ 4,500 g; * Chinese nationality; * Weight and height are within normal range (i.e. WHO Child Growth Standards * 2SD); * No relocation across provinces/ cities in the past 1 year and no plans to relocate during the study period. * Breastfeeding reference: breastfeeding at the time of enrollment, and the mother intends to continue breastfeeding throughout the study period; * Intervention arm: formula feeding / habitual milk drinking (formula milk, milk and other dairy products) at the time of enrollment, and willing to change from the original milk powder / dairy product to the study formula, and consume it as instructed during the study period; * The child's parent(s) / guardian has access to a mobile phone on which the secure digital WeChat platform can be installed and used, connect to the network, take photographs and record defecation, and complete questionnaires during the study; * The child's parent(s) / guardian is of legal age of consent, has sufficient command of Chinese (Mandarin) language to complete the informed consent and other study documents, is willing and able to fulfill the requirements of the study. * The child's parent(s) / guardians can be contacted directly by telephone or WeChat;

Exclusion criteria

* Neonatal asphyxia at birth; * Chronic infectious, metabolic, genetic illness or other disease including any condition that impacts feeding or may impact study outcomes; * Cognitive and developmental disorders; * Antibiotic usage up to 2 weeks before enrollment; * Ongoing antibiotic treatment; * Taking probiotic supplements or formula with probiotics up to 1 month before enrollment; * Participation in other clinical trials; * Parent(s)' / guardian's refusal to participate in the study; * Known or suspected allergy to cow milk, soy or fish

Design outcomes

Primary

MeasureTime frameDescription
Change in stool bifidobacteria level32 daysStool sample analysis

Secondary

MeasureTime frameDescription
Change in stool lactobacillus level32 daysStool sample analysis
Change in stool characteristics32 days• Stool image analysis based on the 4-point Brussels Infant and Toddler Stool Scale (watery, loose, formed, hard, with hard stools indicating worse outcome)
Change in gastrointestinal tolerance32 daysParent reported questionnaire
Satisfaction with the study product32 daysParent reported questionnaire

Countries

China

Outcome results

None listed

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