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临床试验/NCT04286581
NCT04286581已完成不适用

Comparison of Ambu Auragain and I-Gel Supraglottic Airways in Adult Patients at an Ambulatory Surgery Center

University of Minnesota2 个研究点 分布在 1 个国家目标入组 148 人开始时间: 2021年3月22日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
148
试验地点
2
主要终点
Oropharyngeal Leak Pressure (OLP)

研究概览

简要总结

The purpose of this study is to determine if an I-gel laryngeal mask airway (LMA) has a higher oropharyngeal leak pressure compared to an Ambu Auragain in adult patients in an ambulatory surgery center.

详细描述

Patients who are scheduled for elective ambulatory surgery under general anesthesia will be randomized to one of two groups. Group 1 will receive an I-gel laryngeal mask airway (LMA) and group 2 will receive an Ambu Auragain LMA.

研究设计

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

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • undergoing outpatient ambulatory surgery under general anesthesia that is amenable to using a laryngeal mask airway

排除标准

  • non-English speaking patients
  • patients with abnormal airway anatomy

结局指标

主要结局

Oropharyngeal Leak Pressure (OLP)

时间窗: immediately after placement

OLP will be measured immediately after insertion. This will be accomplished by closing the expiratory valve while keeping fresh gas flow at 3 liters/minute until equilibrium is reached. Pressure will be reported in cmH2O.

次要结局

  • Sore Throat(24 hours post-surgery)
  • Time to Placement(time from opening mouth to successful placement (4 hours))

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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