Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Société des Produits Nestlé (SPN)
Age
0–0
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Healthy infant
Full-term (\> 37 weeks gestation)
Birth weight \> 2500 and \< 4500 g
14-60 days of age on enrollment
Singleton birth
Infant's mother has elected not to breastfeed prior to enrollment
Infant exclusively formula-fed for at least 5 days prior to enrollment
Caregiver perceives infant as very or extremely fussy according to perceived fussiness based on the previous 3 days
Caregiver wishes to switch infant's formula
Has not received solid foods
Having obtained his/her legal representative's informed consent
You may not be if
Known or suspected cow-milk allergy
Currently receiving a specialty infant formula (e.g. thickened, extensively hydrolyzed, amino acid-based, metabolic)
Has switched formula more than two times since hospital discharge
Currently experiencing gastrointestinal or respiratory symptoms secondary to an ongoing infection or virus (e.g. gastrointestinal infection, upper respiratory infection, flu)
Congenital illness or malformation that may affect infant feeding and/or growth
Any readmission to hospital (except for hyperbilirubinemia) prior to enrollment
Receiving probiotic supplements
Infant's family who in the Investigator's assessment cannot be expected to comply with treatment (feeding regimen).
Participation in another study that has not been approved as a concomitant study by Nestlé Nutrition.
