Actively Recruiting

Phase Not Applicable
Age: 0 - 1Year
All Genders
ID05902013

Video Laryngoscopy Versus Direct Laryngoscopy for Nasotracheal Intubation in Neonates and Infants With Congenital Heart Disease Under 1 Year Before Cardiac Surgery: A Pilot Study

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

180

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

This research aims to compare the success rate of the first attempt at nasotracheal intubation using video laryngoscopy versus direct laryngoscopy in newborns and infants under 1 year old with congenital heart disease. The study focuses on patients who require nasotracheal intubation during general anesthesia for cardiac surgeries. This pilot study evaluates different intubation methods to improve airway management in this vulnerable population. Participants will be randomly assigned to receive nasotracheal intubation either with a video laryngoscope (using systems like Storz C-MAC Miller or McGrath Video Laryngoscope) or with a direct laryngoscope (using Miller or Macintosh blades). Each method represents a study group, and the procedures will be performed during the scheduled cardiac surgery. During the study, researchers will monitor and record the success rate of the first intubation attempt within 30 minutes. The study involves 60 neonates and infants who will be closely observed throughout their surgery and postoperative intensive care stay. The outcomes will help determine which technique may be more effective for nasotracheal intubation in this patient group.

CONDITIONS

Brief 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
  • Diagnosis of congenital heart disease
  • Scheduled for cardiac surgery
  • Planned postoperative stay in the intensive care unit
Not Eligible

You will not qualify if you...

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

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Implementation

Duration - Up to 30 minutes

Participants undergo nasotracheal intubation using either video laryngoscopy or direct laryngoscopy as part of their cardiac surgery preparation.

1 procedure visit (in-person)

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

T

Thomas Wasserscheid, MD

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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