The Videolaryngoscopy Versus Direct Laringoscopy for Residents Intubation Study

NCT06842082 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1008

Last updated 2026-03-25

No results posted yet for this study

Summary

The usual intubation technique in the operating room is based on direct laryngoscopy, using a standard Macintosh laryngoscope. However, this skill is not easy to acquire and requires adecuate training. Videolaryngoscopes are becoming a widely accepted airway management technique. because offer better view of the glottis and are easy to use. In addition, indirect laryngoscopes are useful for tracheal intubation by novice operators because of the feedback that supervisors can offer during intubation.

The goal of this clinical trial is to learn which intubation technique performed by residents of anesthesia in the operating room is better.

The main questions it aims to answer are:

* Which intubation technique is more effective for achieving first-attempt intubation?
* Which intubation technique results in fewer complications? Researchers will compare both intubation techniques performed by anesthesia residents in the operating room in adult anesthesia cases.

Conditions

  • Intubation Intratracheal
  • Airway Management

Interventions

DEVICE

Intubation with standard laryngoscope

Anesthesia resident will intubate using a standard laryngoscope.

DEVICE

Intubation with video laryngoscope

Anesthesia resident will intubate using a videolaryngoscope (Storz C-MAC, McGrath, Glidescope or other videolaryngoscope)

Sponsors & Collaborators

  • Hospital Clinico Universitario de Santiago

    collaborator OTHER
  • Complexo Hospitalario de Ourense

    collaborator OTHER
  • Complejo Hospitalario Universitario de Pontevedra

    collaborator OTHER
  • Complexo Hospitalario Universitario de A Coruña

    collaborator OTHER
  • Complejo Hospitalario Universitario de Vigo

    collaborator OTHER
  • Fundación de Investigación Biomédica - Hospital Universitario de La Princesa

    collaborator OTHER
  • Hospital Arquitecto Marcide. Ferrol. A Coruña. (Spain)

    collaborator UNKNOWN
  • Hospital Universitario Lucus Augusti

    lead OTHER

Principal Investigators

  • María Bermúdez María Bermúdez López, MD · Hospital Universitario Lucus Augusti

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
SINGLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-16
Primary Completion
2026-03-03
Completion
2026-03-24

Countries

  • Spain

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06842082 on ClinicalTrials.gov