Evaluating the feasibility and safety of video laryngoscopy for routine nasotracheal intubation in neonates - a randomized controlled pilot trial

Not Applicable

Recruiting

• Conditions: P28.5; P22.0; Respiratory failure of newborn; Respiratory distress syndrome of newborn

• Registration Number: DRKS00020792
• Lead Sponsor: niversitätsmedizin Mainz

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2020-02-07
• Last Update Posted: 19 August 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 90

Inclusion Criteria

Indication for endotracheal intubation,
Age < 44 weeks postmenstrual age

Exclusion Criteria

Declined participation,
Equipment failure,
Personnel not confident,
Intubation outside neonatal intensive care unit (NICU) or delivery suite (DR)

Study & Design

• Study Type: interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
First-pass success rate (passing the endotracheal tube through the vocal chords at first attempt)