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

Inclusion Criteria4

  • Age less than 1 year
  • Congenital heart disease
  • Scheduled for cardiac surgery
  • Planned postoperative ICU stay

Exclusion Criteria2

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

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DEVICElaryngoscopy

laryngoscopy for nasotracheal intubation


Locations(1)

Medical University Vienna

Vienna, Vienna, Austria

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT05902013


Related Trials