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Completed

NCT Number: NCT04864665

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

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.

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Key information

Conditions

Age range

Up to 2 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Guangzhou Women and Children's Medical Center, Guangzhou, Guangdong, China

Loading trial locations.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

a formula with prebiotics and milk fat

Dietary Supplement

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

Primary outcomes

  1. Change in stool bifidobacteria level

    Time frame: 32 days

    Stool sample analysis

Secondary outcomes

  1. Change in stool lactobacillus level

    Time frame: 32 days

    Stool sample analysis

  2. Change in stool characteristics

    Time frame: 32 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)
  3. Change in gastrointestinal tolerance

    Time frame: 32 days

    Parent reported questionnaire

  4. Satisfaction with the study product

    Time frame: 32 days

    Parent reported questionnaire

Sponsors and collaborators

Lead sponsor

Danone Nutricia

Industry

Collaborators

  • Nutricia Early Life Nutrition (Shanghai) Co., Ltd

Registry information

Official study title

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

Important dates

Study start
2021
Primary completion
2022
Study completion
2023
First posted
Apr 29, 2021
Registry last updated
Oct 31, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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