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BabyNes Nutrition System Growth Study

Do Infants Fed With BabyNes™ System Grow in Agreement With the World Health Organization (WHO) Reference?

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02178514
Enrollment
120
Registered
2014-06-30
Start date
2014-12-31
Completion date
2017-05-31
Last updated
2018-01-30

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

Conditions

Growth

Brief summary

Our main research question is: Do infants fed with BabyNes Nutrition System grow in agreement with the WHO reference? Our second question is: Do infants fed with BabyNes Nutrition System have a metabolic profile closer to breastfed infants? In order to answer both questions an observational trial will be carried out for 12 months in order to measure weight and to calculate the weight for age z-scores according to the WHO reference. A breastfeeding group will be used as reference for the metabolic parameters measured in blood of infants from Chinese background. The effect of the Babynes formulas will be compared to the metabolic values obtained from this breast-feeding reference group.

Detailed description

Design: 12 months-study, with a breastfeeding group for the comparison of metabolic values obtained from a Chinese Reference population. Number of subjects: In total, 120 subjects shall be enrolled. 80 subjects will be assigned in formula fed group and 40 subjects to breast feeding group. 20% dropouts are already considered for the sample size of 120. Product(s) to be tested: For formula fed group: * BabyNes 1 months: 0-1 month of age * BabyNes 2 months: 1-2 months of age * BabyNes 3-6 months: 3-6 months of age * BabyNes 7-12 months: 7-12 months of age For breast feeding group: * Nan HA 1 once the mothers are no more breastfed from 4 months until 6 months old. * Nan HA 2 once the mothers are no more breastfed from 6 months until 1 year old. Amount, dosage, route of administration, duration of study product: Subjects are included in the study for duration of upto 1 year old of the infant. For FF group: From birth to 4 months, they are exclusively fed with the infant formula dispenser (ad libitum). From 4 months of age they can start diversification but they maintain the adapted infant formula to the age until 12 months. For BF group: Mothers are encouraged to exclusively breast feed the infant up to 6 months old or at least until 4 months old. From 4 months of age, or later than 4 months with no more breastfeeding, they can start Nan HA1 / HA 2 (commercial formula) until the age of 12 months. The amount should be suitable for the age and appetite of the infants.

Interventions

OTHERFormula fed with BabyNes Nutrition System

Sponsors

Société des Produits Nestlé (SPN)
Lead SponsorINDUSTRY

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
OTHER
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
No minimum to 4 Months
Healthy volunteers
Yes

Inclusion criteria

Healthy newborns, whose mothers had a normal BMI before pregnancy and no diabetes Healthy newborn infant. Full term infant (≥ 37 weeks gestation and ≤ 42 weeks gestation). Birth weight ≥ 2500 g and ≤ 4500 g. Having obtained his/her signed legal representative's informed consent. For BF group: * Exclusively breastfed since birth, the infant's mother agrees to exclusively breast feed her infant until at least to 4th month. * Baby is 3 months (3 months ± 7 days) at enrollment. For FF group: * Infant from birth to 21 days of age at the time of enrollment (the 21st day included). * The infant's mother has voluntarily elected to exclusively formula feed her infant after enrolment.

Exclusion criteria

Congenital illness or malformation that may affect normal growth (especially immunodeficiency). Newborn whose mother's BMI was abnormal (\<18.5 or \>23.9) at start of pregnancy. Newborn whose mother has diabetes of type-1 or type-2 or other metabolic disorders. Newborn whose mother has a chronic infectious disease. Newborn whose parents / caregivers cannot be expected to comply with treatment. Newborn currently participating in another nutritional interventional clinical trial (except for vaccination studies).

Design outcomes

Primary

MeasureTime frame
the change in weight-for-age z-score of the WHO Child Growth Standardfrom birth to 4 months of age

Secondary

MeasureTime frame
the Insulin, C-peptide, IGF-1 leptin and ghrelin levelat 4 and 12 months
length and head circumference measuresbirth, 1, 2, 4, 6, 9 12 months of age
Body composition: fat mass, lean mass4 months and 6 months

Countries

China

Outcome results

None listed

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