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临床试验/NCT07453563
NCT07453563招募中不适用

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

University of New Mexico2 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2026年7月13日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
70
试验地点
2
主要终点
Intubation completion time

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult (age ≥18 years)
  • Body Mass Index (BMI) ≥40
  • Scheduled for surgery with general anesthesia

排除标准

  • Pregnancy
  • Congenital facial or airway anomalies
  • History of major neck surgery or tracheostomy
  • History of any lung diseases/conditions such as Chronic Obstructive Pulmonary Disease, lung resection, or lung cancer
  • History of cardiac failure or myocardial infarction
  • Prisoners

研究组 & 干预措施

GlideScope Arm

Active Comparator

Intubation with GlideScope

干预措施: Intubation with GlideScope (Device)

Airway Scope Arm

Experimental

Intubation with Airway Scope

干预措施: Intubation with Airway Scope (Device)

结局指标

主要结局

Intubation completion time

时间窗: Perioperative/Periprocedural

Time interval between the start of the intubation procedure and its completion, defined by confirmed end-tidal carbon dioxide (CO2) observation.

次要结局

  • Humber of hypoxia episodes(Perioperative/Periprocedural)
  • Number of intubation attempts(Perioperative/Periprocedural)
  • Minimum SpO2 observed during intubation(Perioperative/Periprocedural)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Yuta Kashiwagi

Assistant Professor

University of New Mexico

研究点 (2)

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