Oral Supplement for Pregnant and Lactating Mothers

Sponsor
Nestlé (Industry)
Overall Status
Completed
CT.gov ID
NCT01073033
Collaborator
University of the Philippines (Other)
234
1
3
28
8.3

Study Details

Study Description

Brief Summary

To assess protection against early life infections through supplementation of mothers during pregnancy to the newborns' growth, morbidity, immune status intra and extra-uterine.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: milk supplement 1
  • Dietary Supplement: milk supplement 2
N/A

Detailed Description

During pregnancy mothers have to fulfill the tremendous physiological needs to support their own immune status as well as that of their babies. Accordingly, it appears highly valuable to provide mothers with a nutritional supplement during pregnancy and lactation to promote the immune development in newborns, thus reinforcing the infants' defenses.

In that respect, an appropriate maternal diet must provide sufficient energy and nutrients to meet the mother's usual requirements and promote health status, as well as the needs of the growing fetus and beyond for the neonate.

Key organogenesis steps take place during fetal life and many functional features of the immune system are already coded in the genetic asset of the individual. However, at birth the immune system remains fairly immature. An epigenetic, postnatal instruction seems to be extremely important for the maturation of the immune system allowing its full functionality.

The cross-talk between the mother and her baby is, indeed, crucial for the optimal development of the foetus and subsequently for the full and functional maturation of the neonate.

The newborn relies for his protection almost exclusively on his innate immune system that is initially instructed and educated early in life by factors derived from his mother as well as post-natal environmental factors such as early life colonization with micro-organisms that activates the innate immunity and enhance Th1-cell polarization thereby potentially reducing atopic dermatitis with respect to the hygiene hypothesis.

A large part of this immune education is provided by factors transmitted from the mother pre-natally through the placenta or post-natally via the breast milk. Breast milk contains a number of nutrients and bioactive components, including immune cells, maternal antibodies (mainly secretory IgA), cytokines, growth factors, lactoferrin, nucleotides, triacylglycerols, fatty acids, oligosaccharides, and vitamins. All together, these components beneficially impact the health status of the newborn, conferring, among other functions, immune education and early protection.

A typical example of such transfer of immune competence is the TGF-β that could be transmitted in active from either through the placenta or absorbed by the neonates through the milk. This TGF-β is an important IgA switch factor and this is likely to be responsible, in part, for the capacity of breast-fed infant to produce higher levels of mucosal SIgA compared to non-breast fed infants. Moreover, milk soluble CD14 transmitted to the newborn contributes to prime the neonatal gut to modulate the microbial recognition and establishment of endogenous microbiota.

Diarrhea episodes are major manifestation of common infant infections of viral or bacterial aetiology and are a key health concern in paediatrics. As mentioned above there are evidences that some probiotic strains significantly improve diarrheal outcomes in infants, particularly rotavirus diarrhea. In that respect diarrhea occurrence was selected as the primary outcome in the present trial.

Study Design

Study Type:
Interventional
Actual Enrollment :
234 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)
Primary Purpose:
Prevention
Official Title:
Oral Supplement for Pregnant and Lactating Mothers to Promote Infant Immune Maturation and Protection Against Early Life Infections
Study Start Date :
Apr 1, 2010
Actual Primary Completion Date :
Apr 1, 2012
Actual Study Completion Date :
Aug 1, 2012

Arms and Interventions

Arm Intervention/Treatment
Experimental: oral supplement1

Oral supplement for pregnant and lactating mothers

Dietary Supplement: milk supplement 1
milk supplement with probiotics
Other Names:
  • Suitable for pregnant and lactating period.
  • Active Comparator: oral supplement 2

    Oral supplement for pregnant and lactating mothers

    Dietary Supplement: milk supplement 2
    milk supplement without probiotics
    Other Names:
  • Suitable for pregnant and lactating periode.
  • No Intervention: Reference

    No oral supplementation during pregnancy and lactating.

    Outcome Measures

    Primary Outcome Measures

    1. The incidence of diarrhea in infants from birth to 1 year [24 months]

    Secondary Outcome Measures

    1. In infants: growth, morbidity, immune maturation, metabolomics profile [18 months]

    2. In mothers: fetal growth, general health, immune system, metabolomics profile and preterm delivery [18 months]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    N/A and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    Yes
    Inclusion Criteria:
    • Expecting mothers who are in their 6th month of pregnancy

    • Willing to consume 2 x 200 ml of test product daily

    • Willing to exclusively breastfeed until the baby is at least 2-month old

    • Having signed the informed consent

    Exclusion Criteria:
    • Known allergy to cow's milk

    • Subjects previously diagnosed HIV(+) and Hepatitis B (+)

    • Multiple pregnancy

    • High risk pregnancy (pre-eclampsia, diabetes, etc)

    • Currently participating or having participated in another clinical trial during the last 3 months

    • Subjects who consumed pro- and /or prebiotics-containing food/supplement* in the month before inclusion

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Ospital Ng Muntinlupa Manila Philippines

    Sponsors and Collaborators

    • Nestlé
    • University of the Philippines

    Investigators

    • Principal Investigator: Dr. Valerie Guinto, MD, University of the Philippines
    • Principal Investigator: Dr. Jacinto Mantaring, MD, University of the Philippines

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Nestlé
    ClinicalTrials.gov Identifier:
    NCT01073033
    Other Study ID Numbers:
    • 08.10 INF
    First Posted:
    Feb 22, 2010
    Last Update Posted:
    Sep 27, 2012
    Last Verified:
    Sep 1, 2012
    Keywords provided by Nestlé
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 27, 2012