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Clinical Experience With Numeta in Preterm Infants | Clinical Trials | Clareo Health

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COMPLETEDNCT01981057

Clinical Experience With Numeta in Preterm Infants

The aim of this prospective noninterventional study is to evaluate the clinical application of Numeta® in preterm infants and critically ill neonates in comparison to individualized prescribed parente...

Lead sponsor: Medical University of Vienna•1 locations•View source on ClinicalTrials.gov

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Sponsors

Lead Sponsor

Medical University of Vienna

Age

0 - 0 years

Sex

ALL

Healthy Volunteers

No

Inclusion Criteria

•preterm infants \<37 weeks gestational age
•parenteral nutrition therapy

Exclusion Criteria

•hypersensitivity to egg, soy or peanut proteins or to any of the active substances
•congenital abnormality of the amino acid metabolism
•pathogenically elevated plasma concentrations of sodium, potassium, magnesium, calcium and/or phosphorous
•severe hyperglycemia
•severe hyperlipidemia
•severe disorders of lipid metabolism characterized by hypertriglyceridemia

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Data from ClinicalTrials.govLast updated on ClinicalTrials.gov: October 26, 2017Terms

Trial snapshot

StatusCOMPLETED

Phase—

Enrollment50

Start dateFeb 2013

Last updatedOct 26, 2017

Condition

Premature Infants

Locations shown

Medical University of Vienna

Vienna

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Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: October 26, 2017Data synced to Clareo: May 10, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

View ClinicalTrials.gov Terms and Conditions