Infant Formula

3

Review clinical trials related to Infant Formula. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Effect of Partially Hydrolyzed, Whey-based Infant Formulas on Growth and Tolerability in Healthy Term Infants

This study will assess the effect of partially hydrolyzed, whey-based infant formulas on growth and gastrointestinal tolerance in healthy term infants.

Participants needed: 234
Trial details
Age: 0-28Biological sex: AllType: InterventionalSponsor: Société des Produits Nestlé (SPN)Updated: Dec 19, 2025Locations: 3
Eligibility criteria

Written informed consent has been obtained from at least one parent (or other le... [+6]

Chronic infectious, metabolic, genetic illness or other disease, including any c... [+6]

Status: Recruiting

Studying Phenotypic Risks for Obesity and Underlying Traits in Young Infants

The purpose of this research study is to understand how infants metabolize different meals and to develop clinical tools which identify infants as having two different phenotypes. The phenotypes are the 1) metabolic "thriftiness" and 2) the metabolic flexibility.

Participants needed: 40
Trial details
Age: 2-16Biological sex: AllType: ObservationalSponsor: Pennington Biomedical Research CenterUpdated: Aug 22, 2025Locations: 1
Eligibility criteria

Aged 2 weeks to less than 17 weeks at screening [+3]

Unable to complete the screening visit and two clinic visits within 14 days [+4]

Status: Recruiting

Growth, Allergy and Neurodevelopment in Infants on Hydrolysed Formula

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.

Participants needed: 312
Trial details
Age: 4-8Biological sex: AllType: InterventionalSponsor: Umeå UniversityUpdated: Dec 12, 2023Locations: 2
Eligibility criteria

Healthy infants born at term [+2]

Suspected or verified food allergy [+1]