Improved Respiratory Infection by Consuming Lactoferrin Fortified a2 Growing up Formula in Children of 2 to 3 Year Old

February 27, 2024 updated by: a2 Milk Company Ltd.

Improved Respiratory Infection Outcomes Associated With Lactoferrin Fortified a2 Growing up Formula Consumption in Children of 2 to 3 Year Old: a Randomized, Open Label Trial

The goal of this observational study is to compare the incidence of ARI and/or diarrheal disease associated with feeding different formulas with and without lactoferrin supplement in children of 2-3 years old. 200 children eligible for the study will be enrolled from two study sites and randomly assigned to two groups (a2 growing up stage 3 formula puls lactoferrin supplement, and Enfinitas growing up stage 3 formula) to feed for 90 days. About 160 children (80 for each group) are expected to finish the study, and data will be collected during the four visits across the study.

Researchers will compare the two groups to see if there is significant decrease of the occurrence of diarrheal disease and/or acute respiratory infection for children fed with a2 growing up stage 3 formula puls lactoferrin supplement

Study Overview

Detailed Description

This study is two arms, opening parallel-designed, observational study. Diarrheal and infectious episodes, including acute upper and lower respiratory infections (ARI), changes in stool patterns, use of systemic antibiotics, adverse events and study formula consumption will be compared in children 2 - 3 years of age who are assigned to receive one of the two following study formulas for a 3-month feeding period: a2 growing up stage 3 formula puls lactoferrin supplement and Enfinitas growingup stage 3 formula.

200 children eligible for the study will be enrolled from two study sites and randomly assigned to two groups to feed for 90 days. About 160 children (80 for each group) are expected to finish the study, and data of primary and secondary outcomes will be collected during the four visits across the study. A sample size of 80 completed per group is needed to achieve a 80% power.

The Andersen-Gill model will be used to model the primary outcome (recurrent event of either diarrheal disease or an acute respiratory infection) under the framework of the proportional hazard assumption. For other secondary outcomes such as duration of acute respiratory infections(ARI) and/or diarrheal disease, episodes of systemic antibiotic use,amount of study formula consumed,changes in stool pattern and cost of treatment will also be analyzed.

Study Type

Observational

Enrollment (Actual)

200

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Zhejiang
      • Jinhua, Zhejiang, China
        • Qiu Bin Community Hospital
      • Jinhua, Zhejiang, China
        • Nan Quan Community Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

2 years to 3 years (Child)

Accepts Healthy Volunteers

Yes

Sampling Method

Non-Probability Sample

Study Population

Full term born children who are 2-3 years old and consume Milk or milk-based beverage regularly

Description

Inclusion Criteria:

  • Full term born children current aged 2-3 years old
  • Birth weight not less than 2500g (5lb 8oz)
  • Consumes Milk or milk-based beverage regularly before recruitment
  • Informed consent signed
  • Parents or guardians of the infants committ not to participate in interventional clinical research during the intervention

Exclusion Criteria:

  • Has a potential risk of metabolic or chronic disease; Fetal malformation; Or present with condition(s) that the investigator believes may affect the infant's ability to be orally fed, the infant's normal growth/development, or the infant's health evaluation.
  • In-take prebiotics or probiotic continuesly 15 days before the recruitment.
  • Growth problems or other protencial risks.
  • Larger-gestational age (LGA) babies born to mothers with gestational diabetes (defined as newborns whose birth weight is above the 90th percentile of average - Treated with antibiotics 7 days before study intervention.

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Observational Models: Case-Control
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
a2 growing up stage 3 formula puls lactoferrin supplement

per 100g serving

  • Lactoferrin 30 mg
  • Galactooligosaccharides (GOS) at 3 g
  • DHA 0.37
  • Lactoferrin supplement plus: 2.68 ml per serving, 20 mg per 2 ml, 600 mg per bottle
The participants in this group will consume 4-5 scoops (8.5g/scoop) of the assigned formula each time, and 4 times per day
Enfinitas growing up stage 3 formula

per 100g serving

  • Lactoferrin 330 mg
  • Galactooligosaccharides (GOS) at 1.58 mg
  • β-Glucan 22 mg
  • DHA 0.4
The participants in this group will consume 4 scoops (10g/scoop) of the assigned formula each time, and 3 times per day

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change of frequency of acute respiratory infection (ARI) and/or diarrheal disease
Time Frame: baseline day 0, day 90
Change of frequency of acute respiratory infection (ARI) and/or diarrheal disease from baseline to 3 months
baseline day 0, day 90

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Duration of acute respiratory infections(ARI) and/or diarrheal disease
Time Frame: baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Number of days with acute respiratory infections(ARI) and/or diarrheal disease for each visit
baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Number of days of antibiotics treated
Time Frame: baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Number of days of antibiotics treated for each visit interval
baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Amount of study formula consumed
Time Frame: baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Amount of study formula consumed (in grams)
baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Changes in stool pattern
Time Frame: baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Average number of bowel movements per week and stool consistency
baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Cost of medical treatment
Time Frame: baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90
Cost of medical treatment in RMB yuan for each visit interval
baseline day 0, visit 1 day 30, visit 2 day 60, visit 4 day 90

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Xiaoyang Sheng, MD, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

December 19, 2022

Primary Completion (Actual)

May 17, 2023

Study Completion (Actual)

May 17, 2023

Study Registration Dates

First Submitted

December 20, 2022

First Submitted That Met QC Criteria

January 2, 2023

First Posted (Actual)

January 4, 2023

Study Record Updates

Last Update Posted (Actual)

February 29, 2024

Last Update Submitted That Met QC Criteria

February 27, 2024

Last Verified

February 1, 2024

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

Clinical Trials on Respiratory Infection

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