- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06052592
Metabolomic Profile in Breastfed Late Preterm Infants
November 14, 2023 updated by: Giuseppe De Bernardo, Ospedale Buon Consiglio Fatebenefratelli
Metabolomic Profile in Breastfed Late Preterm Infants Versus Standard Formula Milk or Postbiotic-supplemented Formula Milk
Exclusive breast milk is recommended from birth to 6 months of life to promote the development of a balanced intestinal microbiota.
Human milk provides several bioactive components, from natural probiotics such as Bifidobacterium spp.
and Lactobacillus spp., to their metabolites which colonize the intestine of the newborn.
However, if breast milk is not available or insufficient, it is used formula milk as a substitute.
Infant formula can be supplemented with postbiotics to promote maturation of immune, metabolic and microbial components, similar to breast milk.
Postbiotics are preparations composed of both microbial constituents and their metabolites, produced during fermentation.
Study Overview
Status
Completed
Intervention / Treatment
Detailed Description
A balanced nutrition starting from early childhood significantly influences growth and psychomotor development.
Exclusive breast milk is the recommended nutritional choice from birth to 6 months of life, as it guarantees everything necessary for growth, maturation, protection from infections, promoting the development of a balanced intestinal microbiota.
Several prenatal and perinatal factors including the type of delivery, the use of antibiotics, diet and other environmental factors, can influence the microbial colonization of the newborn.
Thus, it is generally accepted that the gut microbiota of the healthy, full-term, vaginally born, breastfed infant is the gold standard for a favorable microbial composition in the early years of life.
Human milk provides several bioactive components, from natural probiotics such as Bifidobacterium spp.
and Lactobacillus spp., to their metabolites ("natural postbiotics"), which colonize the intestine of the newborn.
These metabolites regulate the development of the immune system and attenuate the inflammatory processes.
However, if breast milk is not available or insufficient to meet the nutritional needs of the infant, formula milk is proposed and used as a substitute.
Given the benefits, it is essential that infant formula is as close to human milk as possible, providing bioactive substances that target gut and immune system health.
Current research focuses on optimizing artificial formulas, with the aim of resembling human milk in composition and functionality, with some on the market already including probiotics, prebiotics, synbiotics and postbiotics.
However, it still remains to be clarified which is the best formulation and the exact consequences on the immune, metabolic and microbial system of the newborn.
In particular, postbiotics are preparations composed of both microbial constituents and their metabolites, produced during fermentation.
It has already been highlighted in the literature that the enrichment of formula milk with post-biotics would seem to offer advantages for feeding term infants.
Furthermore, it promotes an immune, metabolic and microbial component maturation, similarly to human milk, thus making postbiotic supplements very promising and interesting in the nutrition of newborns and infants.
Study Type
Observational
Enrollment (Actual)
54
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
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Napoli, Italy, 80123
- Department of Woman and Child, Buon Consiglio Fatebenefratelli Hospital
-
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Naples
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Salerno, Naples, Italy, 84084
- Department of Pharmacy, University of Salerno
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
Infants born at Ospedale Buon Consiglio Fatebenefratelli, Naples
Description
Inclusion Criteria:
- Weight appropriate to gestational age (percentiles >10th and <90th)
- Written informed consent
Exclusion Criteria:
- Cardiological diseases
- Liver disease
- Gastrointestinal diseases with malabsorption
- Endocrinological diseases
- Perinatal infections
- Metabolic and genetic diseases
- Born to mothers with endocrinological and metabolic diseases
- Withdrawal of informed consent
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
|---|---|
|
Group A
Newborns fed with formula milk supplemented with 20 mg/day of fermented FOS from Lactobacillus paracasei strain CNCM I-5220 and Vitamin D (0.5 ml of SMART D3 MATRIX)
|
Newborns will be fed with breast milk, formula milk or postbiotic formula milk
|
|
Group B
Newborns fed with formula milk
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Newborns will be fed with breast milk, formula milk or postbiotic formula milk
|
|
Group C
Newborns fed with exclusive breast milk
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Newborns will be fed with breast milk, formula milk or postbiotic formula milk
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants
Time Frame: 5 days after delivery
|
To detect the differences in the metabolome of the newborns
|
5 days after delivery
|
|
Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants
Time Frame: 1 month after delivery
|
To detect the differences in the metabolome of the newborns
|
1 month after delivery
|
|
Evaluation of metabolomic profile by liquid chromatography mass spectrometry in breastfed late preterm infants
Time Frame: 3 months after delivery
|
To detect the differences in the metabolome of the newborns
|
3 months after delivery
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Collaborators
Investigators
- Principal Investigator: Giuseppe De Bernardo, MD, Ospedale Buon Consiglio Fatebenefratelli
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
March 1, 2022
Primary Completion (Actual)
November 1, 2023
Study Completion (Actual)
November 1, 2023
Study Registration Dates
First Submitted
August 3, 2023
First Submitted That Met QC Criteria
September 18, 2023
First Posted (Actual)
September 25, 2023
Study Record Updates
Last Update Posted (Actual)
November 15, 2023
Last Update Submitted That Met QC Criteria
November 14, 2023
Last Verified
August 1, 2023
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- 1680
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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