The objective of this double blinded randomized study is to assess the tolerance of two extensively protein hydrolyzed infant formulas, one based on rice protein and the other one on casein, at introduction, and after 3 months of consumption, and their efficacy on growth and on the reduction of allergy symptoms through a 3 months consumption period.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
114
Biosearch S.A.
Granada, Spain
Proportion of infants who tolerate either the rice hydrolyzed protein infant formula or a hydrolyzed casein infant formula after 24h consumption.
Tolerance is absence of clinical signs.
Time frame: 24h
Effectivness of the hydrolyzed protein formulas in terms of growth and allergy symptoms improvement.
Evaluate during 3 months of consumption the effectiveness of the formulas, in terms of : * infant growth, through anthropometric measures (body weight, length and head circumference) * allergy symptoms, through the improvement of the allergy symptoms.
Time frame: 3 months
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