Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
Abbott Nutrition
Age
0–0
Sex
ALL
Healthy volunteers
Accepted
You may be eligible if
Participant is judged to be in good health as determined from participant's medical history
Participant is a singleton from a full-term birth with a gestational age of 37 - 42 weeks
Participant's birth weight was ≥ 2490 g (\~5 lbs. 8 oz.)
If parent(s) elect to formula feed the participant they confirm their intention to feed their participant the study product as the sole source of feeding until 4 months of age, and as the sole milk beverage during the first 12 months of life
If parent(s) elect to formula feed the participant, they confirm their intention to feed the participant the assigned toddler drink from 12 months of life to 24 months of life as the primary milk beverage
If parent(s) elect to feed the participant mother's human milk, they confirm that their infant was exclusively fed mother's human milk since birth and confirm their intention to continue exclusively feeding human milk as the sole source of feeding through 4 months of age
If parent(s) of human milk fed participant elect to supplement or wean after 4 months to 24 months of age, they confirm their intention to use the supplemental/weaning formula or toddler drink as the primary milk beverage
Parent(s) of formula-fed participant confirm their intention not to administer vitamin or mineral supplements, from enrollment through the duration of the study
Parent(s) confirm their intention not to administer solid foods or juices to the participant from enrollment through 6 months of age
Participant's parent(s) has voluntarily signed and dated an informed consent form (ICF), approved by an Institutional Review Board/Independent Ethics Committee (IRB/IEC) and provided Health Insurance Portability and Accountability Act (HIPAA) (or other applicable privacy regulation) authorization prior to any participation in the study.
You may not be if
An adverse maternal, fetal or participant medical history that is thought by the investigator to have potential for effects on tolerance, growth, and/or development
Participant is taking and plans to continue medications (including over the counter (OTC), home remedies, herbal preparations, prebiotics or probiotics, or rehydration fluids that might affect GI tolerance
Participant is in another study that has not been approved as a concomitant study
Participant has been treated with antibiotics prior to enrollment
Clareo Health | Infant Formula and Toddler Drink Feeding Intervention
