Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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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