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Clinical Experience With Numeta in Preterm Infants — Numeta  

Premature Infants Clinical Trial

Official title:
Clinical Experience With Numeta- Impact on Intake of Nutrients and Costs

Clinical Trial Summary

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 parenteral nutrition. With the prescription software Cato-PAN® (by Cato software solutions) exact valid prescriptions for ordering parenteral nutrition solutions for premature infants are compared. Each PN solution is prescribed individually as well as with Numeta. Prescriptions were mirrored with respect to weight, venous approach, total volume and amount of enteral feeding, 24h medication and flipped vice versa. The key nutrient for calculating Numeta prescriptions was protein. The results of PN prescriptions were compared with each other/ESPGHAN recommendations. The investigators hypothesize that nutrimental content of Numeta prescriptions is equal to individually prescribed .parenteral nutrition solutions

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01981057
Study type Observational [Patient Registry]
Source Medical University of Vienna
Contact
Status Completed
Phase N/A
Start date February 2013
Completion date November 2013
View Details
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