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The purpose of the study is to test a food supplement to:
Full description
The study involves parents/caregivers of infants, ≥ 5 months but < 11 months of age. Parents who enrolled their infants complete a 1-month blinded placebo run-in period, followed by randomization to placebo or the food supplement.
During the intervention period, infants randomized to the food supplement are fed a once daily, individual packet of the food supplement mixed into liquid (e.g., breast milk, infant formula) or solid (e.g., applesauce, pureed carrots) foods being fed to the infant. The food supplement is a blend of 16 common allergenic proteins ([oat, milk, egg, sesame, wheat] [almond cashew, hazelnut, peanut, pecan, pistachios, soy, walnut] [cod, shrimp, salmon]) combined with 400 IU of Vitamin D3. Parents complete a daily diary about any reactions or symptoms within 2 hours of ingesting the food supplement. Infants randomized to the placebo are also fed a once daily individual packet of the placebo mixed into liquid or solid foods being fed to the infant. Parents also complete a daily diary about any reactions or symptoms within 2 hours of ingesting the placebo.
Enrollment
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Inclusion criteria
Exclusion criteria
Any parent/caregiver who cannot understand or write English.
A parent/caregiver who is in prison.
Any infant who
Has a previous or current diagnosis of food allergy, made by a board-certified allergy and immunology specialist;
Was born before 37 weeks of pregnancy (premature birth);
Has severe eczema, as determined by two parent/caregiver questions:
Has a current serious, chronic condition, as measured by:
If a parent/caregiver has multiple birth infants (e.g., twins), only one eligible infant will be selected.
Any person who works for Before Brands or who has a family member working for Before Brands.
Primary purpose
Allocation
Interventional model
Masking
705 participants in 2 patient groups, including a placebo group
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Data sourced from clinicaltrials.gov
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