RecruitingNot ApplicableNCT05902013

Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation

Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation in Neonates and Infants With Congenital Heart Disease Less Than 1-year of Age Prior Cardiac Surgery: a Pilot Study


Sponsor

Medical University of Vienna

Enrollment

180 participants

Start Date

Sep 21, 2022

Study Type

INTERVENTIONAL

Conditions

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).


Eligibility

Max Age: 1 Year

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a medical device called laryngoscopy for people with airway complication of anesthesia and congenital heart disease. The study is currently recruiting participants at 1 location.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DEVICElaryngoscopy

laryngoscopy for nasotracheal intubation


Locations(1)

Medical University Vienna

Vienna, State of Vienna, Austria

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NCT05902013


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