Actively Recruiting
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
Eligibility Criteria
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
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
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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