Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
Healthy Volunteers
NCT06727513

A Two-Operator Technique for GlideScope-Assisted Endotracheal Intubation

Led by American University of Beirut Medical Center · Updated on 2026-02-06

428

Participants Needed

1

Research Sites

78 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The primary objective of this study is to compare the first attempt success rate of endotracheal intubation using the GlideScope video laryngoscope when performed by two operators versus a single operator. Secondary objectives include assessing the time to intubate, the need for optimization maneuvers, the effect of the presence of predictors of difficult intubation, the occurrence of adverse events during intubation such as oxyhemoglobin desaturation to less than 90% measured by pulse oximetry, the incidence of airway trauma, and the incidence and severity of post-op sore throat. The main question it aims to answer is: Is endotracheal intubation performed using the Glidescope video laryngoscope with an intubating stylet by two operators, non-inferior to the same procedure performed by single operator in terms of first attempt success rate? Researchers will compare first attempt success rate of endotracheal intubation using the GlideScope video laryngoscope when performed by two operators versus a single operator to see if assistance in using the GlideScope provides similar first attempt success rate of endotracheal intubation and thus guarantees securing a difficult airway. Participants will be enrolled in one of two groups over 9 months of work. They will be further stratified into blocks according to the presence of at least one predictor of difficult intubation. Patients allocated to the control group will be intubated using the GlideScope by a single operator and those allocated to the experimental group will be intubated using the GlideScope with the assistance of a second operator.

CONDITIONS

Official Title

A Two-Operator Technique for GlideScope-Assisted Endotracheal Intubation

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 years or older
  • American Society of Anesthesiologists (ASA) Class I to III
  • Scheduled for elective procedures
  • Patients requiring orotracheal intubation with a single-lumen tube under general anesthesia
Not Eligible

You will not qualify if you...

  • American Society of Anesthesiologists (ASA) Class IV or V
  • Emergency procedures
  • Patients requiring awake or asleep fiberoptic intubation
  • Patients requiring nasal intubation
  • Patients requiring double-lumen endotracheal tube
  • Patients already intubated
  • Patients requiring rapid sequence induction due to uncontrolled gastroesophageal reflux disease, hiatal hernia, or full stomach
  • Patients with oropharyngeal or laryngeal pathology such as tumor or abscess
  • Patients with maxillary or mandibular fracture

AI-Screening

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Trial Site Locations

Total: 1 location

1

American University of Beirut Medical Center

Beirut, Lebanon

Actively Recruiting

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Research Team

R

Roland Kaddoum, MD

CONTACT

T

Thuraya HajAli, MSc

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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