Growth and Weight Gain in ELBW Infants Fed an Exclusively Human Milk Based Diet With Prolacta®
NCT ID: NCT03886844
Last Updated: 2019-04-29
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
196 participants
OBSERVATIONAL
2015-12-31
2018-11-30
Brief Summary
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Due to the various benefits of human milk feds to preterm infants, a human milk fortifier based on donor milk (Prolact+6 H2MF® Prolacta, City of Industry, California) has been developed. With this study, the investigators want to evaluate the effect of human milk fortification on weight gain in extremely low birth weight infants (ELBW, \<1000g birth weight) in comparison to bovine fortification.
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Detailed Description
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The composition of breast milk usually meets the nutritional demands of term infants. As preterm infants have enhanced nutritional requirements, multicomponent fortifiers are added to breast milk in order to establish adequate growth and proper neurodevelopmental outcome.
Due to the various benefits of human milk feds to preterm infants, a human milk fortifier based on donor milk (Prolact+6 H2MF® Prolacta, City of Industry, California) has been developed. This human milk fortifier contains more energy and protein than bovine milk fortifiers. So far, accurate data on growth and weight gain under an exclusive diet with human milk and the human milk fortifier Prolact+6H2MF®are missing. With this study, the investigators want to evaluate the impact of a human milk based fortifier on weight gain in extremely low birth weight infants (ELBW, \<1000g birth weight) in comparison to bovine milk based fortifier.
Conditions
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Study Design
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COHORT
RETROSPECTIVE
Study Groups
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Prolacta group
Infants, who received a human milk fortifier based on human milk (12/2015-11/2018), started with an enteral intake of 100 ml/kg until 32 weeks corrected for prematurity
Human milk fortifier based on human milk (Prolacta)
Intervention is started with an enteral intake of 100 ml/kg until 32 weeks corrected for prematurity, afterwards a human milk fortifier based on bovine milk is administered until estimated date of birth or 52 weeks corrected for prematurity (weight \<10. percentile) according to ESPGHAN(=European Society for paediatric gastroenterology, hepatology and nutrition) guidelines
"Frauenmilch Supplement"=FMS group
Infants, who received a human milk fortifier based on bovine milk (05/2012-06/2015), started with an enteral intake of 100 ml/kg
No interventions assigned to this group
Interventions
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Human milk fortifier based on human milk (Prolacta)
Intervention is started with an enteral intake of 100 ml/kg until 32 weeks corrected for prematurity, afterwards a human milk fortifier based on bovine milk is administered until estimated date of birth or 52 weeks corrected for prematurity (weight \<10. percentile) according to ESPGHAN(=European Society for paediatric gastroenterology, hepatology and nutrition) guidelines
Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* Major congenital birth defects
* Major inborn error of metabolism
1 Day
8 Weeks
ALL
No
Sponsors
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Paracelsus Medical University
OTHER
Medical University of Vienna
OTHER
Responsible Party
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Nadja Haiden,MD
Associate Professor for Pediatrics
Principal Investigators
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Assoc. Prof. PD. Nadja Haiden, MD, MSc
Role: PRINCIPAL_INVESTIGATOR
Medical University of Vienna
Locations
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Paracelsus Medical University
Salzburg, , Austria
Medical University of Vienna
Vienna, , Austria
Countries
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Other Identifiers
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Prolacta
Identifier Type: -
Identifier Source: org_study_id
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