Actively Recruiting

Phase Not Applicable
Age: 0 - 1Year
All Genders
NCT05902013

Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation

Led by Medical University of Vienna · Updated on 2025-09-29

180

Participants Needed

1

Research Sites

171 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

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).

CONDITIONS

Official Title

Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation

Who Can Participate

Age: 0 - 1Year
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Age less than 1 year
  • Diagnosed with congenital heart disease
  • Scheduled for cardiac surgery
  • Planned stay in the intensive care unit after surgery
Not Eligible

You will not qualify if you...

  • Nostrils not suitable for nasotracheal intubation
  • Bleeding during dilation of nostrils

AI-Screening

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Trial Site Locations

Total: 1 location

1

Medical University Vienna

Vienna, State of Vienna, Austria, 1090

Actively Recruiting

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Research Team

E

Eva M Base, MD

CONTACT

T

Thomas Wasserscheid, MD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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