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Enfamil NeuroPro Study
Enfamil NeuroPro Study
Active Not RecruitingNA
Sponsor: University of Arizona
Conditions: Infant Development, Infant ALL
Interventions: Enfamil NeuroPro, Enfamil Infant
Countries: United States
This study will compare infant gut bacteria for infants who have been fed a standard infant formula (Enfamil Infant); infants who have been fed a new infant formula designed to be more similar to breast milk (Enfamil NeuroPro); and breastfed infants. These formulas are currently available on the market and meet FDA requirements for infant formula.
Eligibility overview
Sex: ALL
Age: 0 Months to 4 Months
Healthy volunteers: Yes
Study type: INTERVENTIONAL
Eligibility criteria
Inclusion Criteria: * Healthy term infants with parental consent * Parents are able to provide informed consent; own a smart phone and are able to fill out weekly digital questionnaires. Exclusion Criteria: * Prematurity (\<= 36 weeks gestational age) * Babies born through c-section * Any health issues identified at the first postpartum screening * Use of both breast milk and formula * Use of donor breast milk * Parent unwillingness/inability to avoid giving prebiotics, probiotics, symbiotics, and immune-stimulating products to the child for the duration of this study
Locations (1)
- Tucson, Arizona, United States