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Study identifier: NCT07173881 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Effect of a Dairy Product for Pregnant and Lactating Women on the Composition of Human Milk

Condition: Pregnancy  ·  Sponsor: Instituto de Desarrollo e Investigaciones Pediátricas Prof. Dr. Fernando E. Viteri

PhaseNA
Planned participants20
Who can joinFemale, 18 Years to no upper limit
Healthy volunteersYes

About this study

Vulnerable populations, who have deficient diets, may produce human milk (HML) that is not adequate in all nutrients, and this will have consequences on the growth and development of the child. In 2021, at IDIP, a specific milk product for pregnant and lactating women, Super Mil Mamá ( SMM, whole milk powder fortified with multiple vitamins, minerals, and DHA ) was designed and developed as part of a key strategy to incorporate into public policies for the first 1000 days of life. However, the potential benefits of this product have not yet been evaluated at the population level. The main objective is to evaluate the effect of the consumption of a milk product (SMM) designed for pregnant women on maternal nutritional status and the composition of human milk at one month postpartum. Specific objectives include: To compare the concentrations of DHA, Vitamins A, E, and D, Iron, Iodine, Zinc, and Calcium in human milk at one month postpartum of mothers who consumed SSM or not. To compare the concentrations of DHA, Vitamins A, E, D and Zinc in blood and the nutritional status of maternal iron between mothers who consumed SSM and those who did not.

This description comes directly from the study's public registry record.

Talk to the study team

Maria F Andreoli, PhD  ·  542214177324  ·  mfandreoli@gmail.com

Always discuss trial participation with your own doctor first.

Locations (2)

Hospital Interzonal de Agudos General San MartínLa Plata, Buenos Aires, ArgentinaRecruiting
Instituto de Desarrollo e Investigaciones Pediátricas (IDIP) - HIAEP Sor María LudovicaLa Plata, Buenos Aires, ArgentinaRecruiting

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Source record: clinicaltrials.gov/study/NCT07173881