The objective of the study is to assess gastrointestinal tolerance and compliance in infants who require a hydrolyzed formula.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
25
Experimental hydrolyzed infant formula to be fed ad libitum
Northpoint Pediatrics
Indianapolis, Indiana, United States
Metro-Health Medical Center
Cleveland, Ohio, United States
Ohio Pediatric Research Association
Huber Heights, Ohio, United States
Weight maintenance
Time frame: 14 days
Formula volume intake
Time frame: 14 days
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