NCT07453563

Airway Scope vs GlideScope for Intubation in Obese Patients

Comparison of GlideScope and Airway Scope for Intubating Morbidly Obese Patients: A Randomized Controlled Study

• Status: Not Yet Recruiting
• Phase: N/A
• Study type: Interventional
• Enrollment: 70 (estimated)
• Sponsor: University of New Mexico · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

This study compares the time required to complete intubation in obese patients (Body Mass Index 40 or greater) when using either the GlideScope or Airway Scope video laryngoscope device to help place the endotracheal tube.

Detailed description

This is a randomized controlled trial of two video laryngoscope devices when used in patients with high (≥40) Body Mass Index (BMI): Airway Scope (Nihon Kohden) and GlideScope (Verathon Inc.). The study compares several outcomes as proxies for ease of intubation including time to complete intubation, number of attempts needed, minimum peripheral oxygen saturation (SpO2) during intubation, and number of episodes of SpO2 falling below 90% before intubation is completed. The patient population is consenting adult patients with BMI ≥40, who are already scheduled for general anesthesia. Intubations will be performed by attending anesthesiologists or anesthesiology residents. Obesity is a known risk factor for difficult intubation due to anatomical changes caused by increased soft tissue around the face and neck. Obese patients' blood oxygen level can rapidly fall during intubation because these patients often have reduced functional residual capacity, and the acuity of any complications may also be increased because these patients also often have additional comorbidities.

Conditions

• Intratracheal Inbubation

Interventions

Type	Name	Description
DEVICE	Intubation with GlideScope	Intubation performed by anesthesiologist using the GlideScope video laryngoscope device
DEVICE	Intubation with Airway Scope	Intubation performed by anesthesiologist using the Airway Scope video laryngoscope device

Timeline

• Start date: 2026-03-01
• Primary completion: 2027-03-01
• Completion: 2027-03-01
• First posted: 2026-03-06
• Last updated: 2026-03-06

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study