Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
54 participants
OBSERVATIONAL
2022-03-01
2023-11-01
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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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)
Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk
Group B
Newborns fed with formula milk
Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk
Group C
Newborns fed with exclusive breast milk
Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk
Interventions
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Milk
Newborns will be fed with breast milk, formula milk or postbiotic formula milk
Eligibility Criteria
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Inclusion Criteria
* Written informed consent
Exclusion Criteria
* 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
34 Weeks
37 Weeks
ALL
No
Sponsors
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University of Salerno
OTHER
Ospedale Buon Consiglio Fatebenefratelli
OTHER
Responsible Party
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Giuseppe De Bernardo
Head of Department of Woman and Child
Principal Investigators
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Giuseppe De Bernardo, MD
Role: PRINCIPAL_INVESTIGATOR
Ospedale Buon Consiglio Fatebenefratelli
Locations
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Department of Pharmacy, University of Salerno
Salerno, Naples, Italy
Department of Woman and Child, Buon Consiglio Fatebenefratelli Hospital
Napoli, Napoli, Italy
Countries
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Other Identifiers
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1680/CE Lazio 1
Identifier Type: -
Identifier Source: org_study_id
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