This is a prospective, double blind, crossover study in healthy infants randomized to one of two study formulas. The trial will consist of two 21 day study feeding periods separated by a study washout period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Masking
QUADRUPLE
Enrollment
91
Fed ad libitum
Fed ad libitum
Tuscon Medical Center
Tuscon, Arizona, United States
Northpoint Pediatrics
Indianapolis, Indiana, United States
Midwest Children's Health Research Institute
Lincoln, Nebraska, United States
MetroHealth Medical Center
Cleveland, Ohio, United States
Carotenoid Concentration
Plasma sample
Time frame: Change from Baseline to end of Study Period A (~21 Days)
Carotenoid Concentration
Plasma sample
Time frame: Change from Baseline to end Study Periods A (~21 Days) and B (~21 Days)
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Dayton Clinical Research
Dayton, Ohio, United States
Institute of Clinical Research
Mayfield Heights, Ohio, United States