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Clinical Trials/NCT04306263
NCT04306263
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Evaluation of the Effect of a New Infant Formula With Specific Ingredients on the Development of the Immune System and the Gastrointestinal Health of the Infant

Laboratorios Ordesa1 site in 1 country231 target enrollmentMarch 2, 2020
ConditionsInfant Growth

Overview

Phase
N/A
Intervention
Not specified
Conditions
Infant Growth
Sponsor
Laboratorios Ordesa
Enrollment
231
Locations
1
Primary Endpoint
Register of diarrhea episodes
Last Updated
5 years ago

Overview

Brief Summary

The purpose of this study is to test whether the addition of certain bioactive ingredients to a new infant formula (HMOs, osteopontin and probiotics) can have a favorable impact on the development of the infant's immune system in the first months of life.

Detailed Description

Nowadays, almost all commercial infant formulas resemble the "gold standard" of breast milk in terms of composition of essential nutrients, but it is still a challenge to identify and incorporate certain bioactive components capable of replicating those stimuli typical of breast milk that can program growth, infant development and maturation of the immune system. The purpose of this study is to test whether the addition of certain bioactive ingredients to a new infant formula (HMOs, osteopontin and probiotics) can have a favorable impact on the development of the infant's immune system in the first months of life. In addition, considering that the quality of feeding at these early ages will program (Early programming) the health and physiology of the child and the future adult, the study wants to obtain evidence of the effects of this new infant formula on the immune system and the development of the child compared to breast milk during the first year of life, hoping that it promotes proper growth, adequate cognitive development and maturation of the immune system as similar as possible to children fed to the mother's breast.

Registry
clinicaltrials.gov
Start Date
March 2, 2020
End Date
September 2022
Last Updated
5 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Laboratorios Ordesa
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Inclusion age from 0 to 2.5 months of age.
  • Gestational age \>37 weeks and \<41 weeks inclusive.
  • Appropriate birth weight appropriate for your gestational age (between 10-90 percentiles).
  • APGAR score normal birth to 1' and 5' of 7 -
  • Umbilical pH ≥ 7.
  • Availability to continue throughout the study period.
  • Written informed consent
  • Additional Inclusion Criteria for groups 1 and 2:
  • Infants who, at the time of recruitment, have already passed the diet with a majority or exclusive formula for medical reasons, by decision of the parents or any other reason agreed with the pediatrician.
  • Additional Inclusion Criteria for group 3 (breastfeed infants):

Exclusion Criteria

  • Simultaneous participation in other clinical trials.
  • Infants suffering from gastrointestinal disorders (allergy and/or intolerance to cow's milk protein or lactose).
  • Mother's pathology history and during gestation: neurological diseases, metabolic disorders, type 1 diabetes mellitus, chronic disease (hypothyroidism), maternal malnutrition, TORCH syndrome.
  • Treatment of the mother's anxiolytics or antidepressants. Other treatments with drugs potentially harmful to neurodevelopment.
  • Inability of the parents to follow up the study (medical decision).

Outcomes

Primary Outcomes

Register of diarrhea episodes

Time Frame: From baseline to 12 months.

Presence and duration of diarrhea, registered in patients dairies.

Register of fever episodes

Time Frame: From baseline to 12 months.

Presence and duration of the fever and treatments, through diaries completed by parents

Register of infections

Time Frame: From baseline to 12 months

Register of infant infections through patient diaries completed by parents

Secondary Outcomes

  • Obstetric background(Baseline)
  • Study of the infant microbiota(At 3, 6 and 12 months.)
  • Immune response evaluation(At 3, 6 and 12 months of age)
  • Demographic data(From baseline to 12 months.)
  • Infant neurodevelopment(At 12 months)
  • Infant neurodevelopment 2(At 2, 3, 4, 6, 9 and 12 months of age.)
  • Assessment of normal growth of the infant(From baseline to 12 months.)
  • Infant neurodevelopment 3(At 2, 3 and 4 months of life.)
  • Infant neurodevelopment 5(12 months of age)
  • Infant neurodevelopment 4(6 and 12 months of age)

Study Sites (1)

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