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Clinical Trial Summary

The purpose of this study is to evaluate the effect of maternal supplementation with 400,000 IU of oral retinol palmitate in the post-partum, the nutritional situation of the binomial mother-child, on growth and morbidity of children in breastfeeding in the first six months of life.


Clinical Trial Description

The effect will be assessed by the milk and blood. ;


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT00742937
Study type Interventional
Source Instituto Materno Infantil Prof. Fernando Figueira
Contact
Status Completed
Phase Phase 2/Phase 3
Start date July 2007
Completion date December 2008

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