Efficacy of a New Infant Formula Composition on Gut Health in Infants
Sponsor: FrieslandCampina • ClinicalTrials.gov ID: NCT07242508
Recruiting for Similar Conditions?
Sponsors are looking for patients like you. See if you qualify for compensated research studies.
Check Eligibility →Description
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
Interventions
-
Infant Formula
(Other)
ad-libitum consumption of infant formula
-
Infant Formula with bioactive ingredients
(Other)
ad-libitum consumption
Eligibility criteria
Conditions
Locations
- Second SAGBAL Sheinovo AD — Sofia, Bulgaria
Partner with Nurenyx
Showcase your study to thousands of motivated patients matching your criteria.
Learn MoreOfficial Source
Data sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
View Official Record