Nutritional Requirements Clinical Trial
Official title:
The Clinical Effects of an Infant Formula Supplemented With Various Concentrations of Nucleotides
The study hypothesis is that different concentrations of nucleotides' supplementation of an infant formula might affect differently growth and/or other clinical parameters in neonates.
Status | Completed |
Enrollment | 150 |
Est. completion date | October 2007 |
Est. primary completion date | |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Both |
Age group | N/A to 30 Days |
Eligibility |
Inclusion Criteria: - Healthy newborns aged 0-30 days. Exclusion Criteria: - Prematurity - Chronic illness - Failure to thrive - Milk allergy |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Prevention
Country | Name | City | State |
---|---|---|---|
Israel | Soroka Medical Center | Beer-Sheva |
Lead Sponsor | Collaborator |
---|---|
Soroka University Medical Center | Materna Laboratories |
Israel,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Growth percentiles, Behaviour and infantile colic, Bowel habits. | |||
Secondary | Side effects. |
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