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Recruiting Not applicable

Video Versus Direct Laryngoscopy for Tracheal Intubation in Pediatric Surgery

NCT07495436 · tracked via the Priya Life Science Spain tracker
Phase
Not applicable
Started
2026-06-01
Last updated
2026-09-21

Condition(s) studied

Tracheal IntubationVideolaryngoscopyGeneral AnesthesiaDifficult Airway Intubation

Investigational drug(s) / intervention(s)

VideolaryngoscopeDirect Laryngoscope

Videolaryngoscope: For patients assigned to the videolaryngoscope Group, the operator will use a video laryngoscope on the first laryngoscopy attempt.

Direct Laryngoscope: For patients assigned to the laryngoscope Group, the operator will use a Macintosh laryngoscope on the first laryngoscopy attempt.

Study summary

Tracheal intubation in paediatric patients is a high-risk procedure in which failure to achieve successful intubation on the first attempt is associated with an increased risk of complications, including hypoxaemia and airway trauma. Videolaryngoscopes have been increasingly adopted in clinical practice because they improve glottic visualisation; however, evidence of their benefit in paediatric patients remains inconsistent.

The VIDEOKIDS trial is a large, pragmatic, international, multicentre, randomised controlled trial designed to compare videolaryngoscopy with direct laryngoscopy as the initial technique for tracheal intubation in paediatric patients undergoing surgery under general anaesthesia. The primary objective is to determine whether videolaryngoscopy increases the rate of successful intubation on the first attempt compared with direct laryngoscopy.

Eligibility

Sex
ALL
Min age
0 Days
Max age
16 Hours
Healthy volunteers
No
Inclusion Criteria: * Paediatric patients (age 0-16 years), * Undergoing elective or scheduled surgery under general anaesthesia requiring orotracheal intubation, * Planned tracheal intubation using either videolaryngoscopy or direct laryngoscopy as the initial technique, * Informed or general consent given, according to the relevant ethics committee statement,. Exclusion Criteria: * Known upper airway anatomical abnormalities or clinical conditions requiring a specific intubation technique (e.g., fibreoptic intubation), * Requirement for emergent tracheal intubation that does not allow adequate randomisation, * Refusal of parents or legal guardians to participate in the study.

Primary outcome measure(s)

  • Number of intubations with successful tracheal intubation on the first attempt — Duration of procedure of procedure (minutes)
    The primary outcome is successful tracheal intubation on the first attempt, defined as placement of an endotracheal tube in the trachea following a single insertion of the laryngoscope blade into the mouth, without its removal.

Trial sites (1)

FacilityCityRegionStatus
Hospital Clínico Universitario de Santiago de Compostela Santiago de Compostela A CORUÑA Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07495436 on ClinicalTrials.gov ↗ ← All trials in Spain