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临床试验/NCT05298228
NCT05298228Unknown不适用

Dose Finding Study of Remimazolam for Laryngeal Mask Airway Insertion

Yonsei University1 个研究点 分布在 1 个国家目标入组 25 人开始时间: 2022年3月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
25
试验地点
1
主要终点
Dose of remimazolam associated with 50% (ED50) probability for adequate depth of anesthesia for LMA insertion without muscle relaxants.

研究概览

简要总结

Laryngeal mask airways (LMA) are widely used in patients receiving general anesthesia and are known to have the following advantages over the endotracheal tube: lower incidence of postoperative sore throat, lower incidence of cough during emergence, and lower incidence of postoperative vomiting. Although LMAs can be inserted without the use of muscle relaxants, a sufficient depth of anesthesia is necessary for placement. Remimazolam is a newer anesthetic that is ultra-short acting with a rapid onset and short context-sensitive half-life allowing for fast recovery. However, the dose of remimazolam needed for LMA insertion without muscle relaxants is not well known. This dose-finding study aims to find the ED50 and ED95 of a single bolus dose of remimazolam for LMA insertion without muscle relaxants in adult patients.

This is an interventional study done in a single group using the Dixon's up-and-down method which requires at least six success/failure pairs in the same direction. The primary endpoint of this study is to investigate the dose of remimazolam associated with 50% (ED50) and 95% (ED95) probability for adequate depth of anesthesia for LMA insertion without muscle relaxants. The beginning dose of remimazolam is 0.3 mg/kg, and when LMA insertion is successful, the dose will be decreased by 0.05 mg/kg in the next patient. When LMA insertion is unsuccessful (failed), the dose will be increased by 0.05 mg/kg in the next patient. Successful LMA insertion is defined as symmetrical chest wall movement and square-wave capnographic traces observed with manual ventilation.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Other
盲法
None

入排标准

年龄范围
19 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients aged 19~65 year
  • ASA class I~III
  • Patients scheduled for orthopedic surgery under general anesthesia and eligible for LMA use.

排除标准

  • Patient refusal
  • Patients unable to read consent form
  • Anticipated difficult mask ventilation
  • Active URI or uncontrolled asthma
  • Pneumonia
  • Risk of aspiration such as GERD
  • History of allergies to benzodiazepines
  • Decreased liver or kidney function
  • Pregnant or breastfeeding patients
  • BMI > 30kg/m2
  • History of substance abuse/addiction

研究组 & 干预措施

Remimazolam

Experimental

A bolus dose of remimazolam is administered to facilitate LMA insertion

干预措施: Remimazolam bolus does administration (Drug)

结局指标

主要结局

Dose of remimazolam associated with 50% (ED50) probability for adequate depth of anesthesia for LMA insertion without muscle relaxants.

时间窗: During procedure (Immediately after LMA insertion attempt)

The primary outcome of this study will be determined based on the data of "success" or "failure" of LMA insertion at predetermined doses of remimazolam. Successful LMA insertion is defined as symmetrical chest wall movement and square-wave capnographic traces observed with manual ventilation which will be assessed immediately after LMA insertion attempt.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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