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
Gestational age at birth less than 37 weeks
Birth weight less than 3200 g (approximately 7 pounds)
Postmenstrual age is 34 0/7 through 41 0/7 weeks at enrollment
Parent(s) confirm their intention to feed their infant the study product as the sole source of nutrition for the duration of the study
The currently-fed formula is a milk-based infant formula at a caloric density of ≤ 24 Cal/fl oz.
Singleton, twin, or triplet births only.
Parent(s) confirm their intention not to administer solid foods or juices to their infant from enrollment through the duration of the study, unless instructed otherwise by their healthcare professional.
Participant's parent(s) has voluntarily signed and dated an ICF, approved by an IRB/IEC and provided 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 taking medications, home remedies, herbal preparations, prebiotics or probiotics, rehydration solutions, or parenteral nutrition
Participant is known to require elective surgery with hospitalization, other than uncomplicated outpatient surgery, during the course of the study.
Participant is in another study that has not been approved as a concomitant study
Participant has an allergy or intolerance to any ingredient in the study product
Participant is currently receiving oxygen therapy
Participant is currently receiving antibiotics
Participant is currently receiving tube feedings
Clareo Health | Evaluation of Preterm Infants Fed Post-Discharge Preterm Infant Formula
