Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation

Status Recruiting

Clinical Trial Summary

The aim of this study is to perform a pilot study investigating the first attempt intubation success rate differing between video laryngoscope nasotracheal intubation and direct laryngoscope nasotracheal intubation. The study population will consist of 60 neonates and infants with congenital heart disease less than 1 year of age who need nasotracheal intubation during general anesthesia for cardiac procedures. Standard nasotracheal intubation will be performed using either a video laryngoscope or direct laryngoscopy. Neonates and infants will be randomly assigned (1:1) to standard video laryngoscopy (with one of the following systems: Storz C-MAC Miller Video Laryngoscope, Karl Storz, Tuttlingen, Germany or Mc Grath Video Laryngoscope, Medtronic, Boulder,USA) or to direct laryngoscopy with one of the following blades: Miller or Macintosh (Heine, Hersching, Germany).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05902013
Study type	Interventional
Source	Medical University of Vienna
Contact	Eva M Base, MD
Phone	+43140400
Email	eva.base@meduniwien.ac.at
Status	Recruiting
Phase	N/A
Start date	September 21, 2022
Completion date	December 31, 2023

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