Healthy Infants
Conditions
Brief summary
This trial is a single-blind, randomized, controlled, parallel-designed trial to compare the effects of a2 Platinum® stage 1 infant formula versus conventional, A1 and A2 β-casein-containing stage 1 infant formula versus breastfeeding on crying, tolerance, gut health, and immune function.
Detailed description
The protocol was updated from V8.2 to V9.1 and was approved by the Ethical Committee of Shanghai First Maternity and Infant Hospital, the main site. The major changes are: from blind to participants to non-blind to participants; from Single-Centre to Multi-Centre; number of subjects from 270 to 180; trial period from 3 weeks to 4 weeks; and number of visits from 6 to 4.
Interventions
OTHERa2 Platinum® stage 1 infant formula
Upon randomization (if not included in the breastfed group), each participant will be provided with up to 105 days' supply of the standardized formula and up to 28 days' supply of the allocated formula. Participants and study investigators will conduct the trial via a pre-determined randomization schedule.
OTHERConventional, A1 and A2 β-casein containing stage 1 infant formula
Upon randomization (if not included in the breastfed group), each participant will be provided with up to 105 days' supply of the standardized formula and up to 28 days' supply of the allocated formula. Participants and study investigators will conduct the trial via a pre-determined randomization schedule.
Sponsors
Shanghai First Maternity and Infant Hospital
Xinhua Hospital, Shanghai Jiao Tong University School of Medicine
Edanz Group Japan Ltd
Women & Children's Health Care Hospital of Linyi, China
Beijing Esmile Technology Co. Ltd.
Nanjing Maternity and Child Health Care Hospital
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine
Second Hospital of Jilin University
a2 Milk Company Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
TRIPLE (Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
0 Days to 76 Days
Healthy volunteers
Yes
Inclusion criteria
1. 0-76 days of age after birth, inclusive (day of birth is considered day 0) 2. Singleton birth 3. Gestational age of 37-42 weeks (36 weeks and six days is considered 36 weeks gestational age) 4. Birth weight of 2,500 g to 4,500 g 5. Signed informed consent obtained for infant's participation in the survey 6. Parent or guardian of infant agrees not to enrol infant in another interventional clinical survey while participating in this survey 7. Parent or guardian agrees to formula-feed the baby as per the randomization schedule For the formula-fed groups, participants in addition to the above-listed criteria, must also meet the following criterion: \- Parent or guardian agrees that the baby will be fed with standardized formula upon enrolment and switched to randomized formula at baseline (90-105 days of age) For the breastfed group, participants in addition to the above-listed criteria, must also meet the following criterion: \- Parent or guardian agrees that the baby will be breast-fed
Exclusion criteria
1. Infant with inborn malformation and with hereditary and/or chronic and/or inborn diseases that could interfere with the survey (e.g. being unable to breast-feed or formula-fed) 2. Diseases jeopardizing intrauterine growth 3. Known or increased risk of IgE-mediated cow's milk protein allergy 1. (i.e. one of the biological parents and/or siblings diagnosed with similar allergy, 2. asthma, hay fever, etc.) 4. Infant with an acute infection or gastroenteritis at time of randomization 5. Evidence of feeding difficulties or formula intolerance, such as vomiting or poor intake at time of randomization 6. Participation in another clinical trial 7. Investigator's uncertainty about the willingness or ability of the parents to comply with the protocol requirements (including to fill in the diaries and to wait with introducing weaning foods until 4 months of age, and capability and willingness to do stool sample collection, handling, processing, and storage as instructed) 8. Infant is immunocompromised (according to a doctor's diagnosis of immunodeficiencies such as combined immunodeficiencies, DiGeorge Syndrome, Wiskott-Aldrich syndrome, severe congenital neutropenia and secondary immunodeficiencies linked to HIV infection, Down Syndrome or others) and children with known head/brain disease/injury such as microcephaly, macrocephaly or others Exit Criteria: 1. Ineligibility (either arising during the trial or retrospectively having been overlooked at screening) 2. Significant protocol deviation 3. Significant non-compliance with product regimen or trial requirements 4. An adverse event (including one occurring before the start of the trial period) which requires discontinuation of the trial product or results in inability to continue to comply with trial procedures 5. Disease progression which requires discontinuation of the trial product or results in inability to continue to comply with trial procedures 6. Withdrawal of Consent 7. Lost to follow up 8. Weight at Visit 2 is \<95% of birth weight \[(weight at Visit 2÷birth weight) x 100 \<95%\] 9. Use of antibiotics, steroids or prebiotics/probiotics anytime between 14 days before baseline and trial completion 10. Participant whose mother has used any form of antibiotics or steroids while breastfeeding 11. More than 1 feed of formula milk per day for the breastfed group 12. More than 2 feeds of breast milk per day for the formula groups
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Changes of crying frequency at each follow up visit compared to baseline | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 days after baseline); Visit 4 (28 days after baseline) | Record frequency of crying (times/d) |
| Changes of crying duration at each follow up visit compared to baseline | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Record duration of crying (min) |
| Changes in fecal MPO levels at each follow up visit compared to baseline | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Record fecal MPO (in Unit) as markers of inflammation |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Changes in head circumference | Visit 1 (screening/randomization); Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Differences in head circumference (cm/d) |
| Changes in salivary cortisol levels at each follow up visit compared to baseline | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Record salivary cortisol (nmol/L) as markers of immune function |
| Abundance analysis of gut microflora species | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 days after baseline); Visit 4 (28 days after baseline) | Differences in abundance of gut microflora species |
| Number of adverse events at each follow up visit compared to baseline | Visit 1 (screening/randomization); Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Record number of adverse events as a measure of safety and tolerability |
| Changes in body length | Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 days after baseline); Visit 4 (28 days after baseline) | Differences in length gain (cm/d) |
| Changes in body weight | Visit 1 (screening/randomization); Visit 2 (baseline [90-105 days since birth]); Visit 3 (14 day after baseline); Visit 4 (28 days after baseline) | Differences in weight gain (kg/d) |
Countries
China
Outcome results
None listed