Efficacy of a New Infant Formula Composition on Gut Health in Infants

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age0-3
SponsorFrieslandCampina

About this trial

The aim of this study is to investigate potential health benefits of the experimental formula. The main objective is whether the experimental formula elevates the relative abundance of Bifidobacterium in stool samples after 10 weeks, as compared a standard formula, aka control formula. In addition other markers of gut health, such as stool characteristics, and gut health symptoms will be monitored

Eligibility criteria

Qualifiers

Healthy, full term, infants with a birth weight between 2500-4500 grams

Parents independently from study decided to not breastfeed their infant

Parents agree to feed the assigned study formula as the infant's sole source of nutrition for the duration of the study

have read and voluntarily signed an informed consent form

Disqualifiers

suffering from any anatomic and/or physiologic condition that would interfere with normal growth, development or feeding

are required to take medications or supplements known to influence growth and development

have a maternal history with known adverse effects on the fetus and/or the newborn infant

have previous or current antibiotics use (antibiotics administered during delivery are permitted)

Trial design

Treatments tested in this trial

  • Infant Formula
  • Infant Formula with bioactive ingredients

Treatment groups

120 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators