Growth, Allergy and Neurodevelopment in Infants on Hydrolysed Formula

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age4-8
SponsorUmeå University

About this trial

Breastfeeding is the recommended diet for all infants during the first half of infancy and is associated with numerous health benefits. However, when breastfeeding is not possible, an infant formula is the only nutritive alternative. Formula-fed infants have a different growth pattern compared to breastfed infants. Studies have shown that the higher protein content in infant formula compared to breastmilk results in a more rapid weight gain and an increased risk of overweight and obesity in childhood. For this reason, both quantity and quality of protein in infant formulae have been optimized during the last decade, to better meet the needs of infants and to support growth close to that of breastfed infants.

Protein hydrolysis, a common modification of infant formulae, has originally been developed for treatment of cow's milk protein allergy. Certain hydrolysed formulae have been suggested to prevent atopic eczema when given to infants with a family history of allergic disease but as of yet, the allergy preventive effect in infants without increased risk of allergic disease has been little studied. Partially hydrolysed infant formulae have also been suggested to reduce common functional gastrointestinal symptoms in infants.

New protein hydrolysates are continually developed for use in infant formulae, with the aim of reducing allergenicity, while ensuring optimal growth and development of infants. It is important to study the effects on growth and health outcomes in infants who are fed formulae based on these newly developed hydrolysates as compared to those fed standard intact protein formulae or breastmilk.

The overall aims of the current study are to evaluate the effects of two new hydrolysates on growth, immunological biomarkers, neurodevelopment, protein metabolism and gut microbiota in a randomized, controlled clinical trial of healthy infants. In compliance with European Food Safety Authority (EFSA) regulations for novel infant formulas based on hydrolysed protein, the primary outcome is change in weight standard deviation score (SDS) from baseline until 5 months of age.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Healthy infants born at term

Birth weight 2500 to 4500 gram

Either exclusive breast-feeding (reference group) or exclusive formula-feeding (intervention and control group)

Disqualifiers

Suspected or verified food allergy

Suspected or verified infant colic

Trial design

Design model

Parallel

Treatments tested in this trial

  • Partially hydrolysed formula

    Dietary supplement

    Partially hydrolysed formula

Treatment groups

312 Participants
are divided into 4 treatment groups
Group A: Study formula 1Experimental treatment 1 intervention
Group B: Study formula 2Experimental treatment 1 intervention
Group C: Standard formulaNo intervention 0 interventions
Group D: Breast feedingNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Weight

Primary outcome is weight Standard Deviation Score (SDS) at the end of the intervention.

Time frame
At 5 months of age

Secondary outcomes

1

Length.

Growth pattern during the course of the intervention measured by length in centimeters and SDS.

Time frame
At enrollment at 2 months of age and monthly during the intervention up to 5 months of age.
2

Head circumference.

Growth pattern during the course of the intervention measured by head circumference in centimeters and SDS.

Time frame
At enrollment at 2 months of age and monthly during the intervention up to 5 months of age.
3

Body composition

Assessing differences in body composition between study groups using fat percentage as measured by PeaPod (Pletysmography).

Time frame
At 4 months of age
4

Gastrointestinal tolerance.

Gastrointestinal tolerance using diary for information about stool frequency and consistency (in four grades from diarrhea to hard stools) in combination with questionnaire filled in by the parents based on Rome IV criteria for functional gastrointestinal disorders.

Time frame
At enrollment at 2 months of age and during the intervention up to 5 months of age.

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Umeå University

Lead sponsor

Lund University

Collaborator

Arla Foods

Collaborator