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Clinical Trial Summary

The overall aim of this study is to determine the differences between two surfactant administration catheters in preterm infants.


Clinical Trial Description

In this single-center, open-label, randomized-controlled trial, preterm infants requiring surfactant administration after birth, using a standardized minimal invasive protocol, were randomised to two different modes of endotracheal catheterization: Flexible Ch-4 feeding tube inserted using Magill forceps (group 1) and semi-rigid catheter (group 2). Primary outcome was duration of laryngoscopy. Secondary outcomes were complication rate and vital parameters during laryngoscopy. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05024435
Study type Interventional
Source Salzburger Landeskliniken
Contact
Status Completed
Phase N/A
Start date November 1, 2019
Completion date April 30, 2020

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