- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05670678
Improved Respiratory Infection by Consuming Lactoferrin Fortified a2 Growing up Formula in Children of 2 to 3 Year Old
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
Status
Conditions
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
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
Zhejiang
-
Jinhua, Zhejiang, China
- Qiu Bin Community Hospital
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Jinhua, Zhejiang, China
- Nan Quan Community Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
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
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
|
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
|
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
Sponsor
Investigators
- Principal Investigator: Xiaoyang Sheng, MD, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Publications and helpful links
General Publications
- Gibson GR, Roberfroid MB. Dietary modulation of the human colonic microbiota: introducing the concept of prebiotics. J Nutr. 1995 Jun;125(6):1401-12. doi: 10.1093/jn/125.6.1401.
- Li F, Jin X, Liu B, Zhuang W, Scalabrin D. Follow-up formula consumption in 3- to 4-year-olds and respiratory infections: an RCT. Pediatrics. 2014 Jun;133(6):e1533-40. doi: 10.1542/peds.2013-3598. Epub 2014 May 19.
- Leyer GJ, Li S, Mubasher ME, Reifer C, Ouwehand AC. Probiotic effects on cold and influenza-like symptom incidence and duration in children. Pediatrics. 2009 Aug;124(2):e172-9. doi: 10.1542/peds.2008-2666. Epub 2009 Jul 27.
- Boehm G, Lidestri M, Casetta P, Jelinek J, Negretti F, Stahl B, Marini A. Supplementation of a bovine milk formula with an oligosaccharide mixture increases counts of faecal bifidobacteria in preterm infants. Arch Dis Child Fetal Neonatal Ed. 2002 May;86(3):F178-81. doi: 10.1136/fn.86.3.f178.
- Cheng JB, Wang JQ, Bu DP, Liu GL, Zhang CG, Wei HY, Zhou LY, Wang JZ. Factors affecting the lactoferrin concentration in bovine milk. J Dairy Sci. 2008 Mar;91(3):970-6. doi: 10.3168/jds.2007-0689.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 22-SM-11-A2-001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
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