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临床试验/NCT05478122
NCT05478122已完成不适用

Soft Mist Spray Device for Airway Anaesthesia During Awake Videolaryngoscopy

Radboud University Medical Center1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年7月25日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
20
试验地点
1
主要终点
Complete anaesthesia of the airway as evaluated with successful awake videolaryngoscopy with minimal discomfort for the subject

研究概览

简要总结

Rationale:

Effective and fast topical anaesthesia of the upper airway is of paramount importance in awake (conscious) videolaryngoscopy of the airway in order to avoid patient discomfort. Different methods of anesthetizing the airway have been described. Conventional topical airway anaesthesia is not always effective due to non-optimal flow patterns and generation of ineffective local anaesthetic aerosols. Other methods of anaesthetizing the airway are more invasive. In order to optimize topical anaesthesia of the airway a soft mist spray device (Trachospray) for topical anaesthesia of the airway has been developed, in which optimal airflow patterns are obtained and local anaesthetic aerosols are generated which will reach the target zone for anesthetizing the airway.

Objective: In this study, the Trachospray will be used for awake videolaryngoscopy, to evaluate its use, effectiveness and comfort level for patients and anaesthesiologist.

Study design: Interventional study.

Study population: 20 healthy human volunteers, ASA 1, 18-60 years old.

Intervention: Subjects will be asked to inhale 4 ml lidocaine 4% via the Trachospray device

Main study parameters/endpoints:

Anaesthesia of the airway as evaluated with successful awake videolaryngoscopy with minimal discomfort for the subject.

Nature and extent of the burden and risks associated with participation:

Risk management on the Trachospray device shows that all user risks are mitigated and no residual risks remain for the use of the device. Testing of the device and the application of the device in daily practice has no additional risks than the present technique of performing anaesthesia of the airways.There may be some discomfort during the procedure, mainly airway irritation which may cause coughing or gag reflex.

研究设计

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

入排标准

年龄范围
18 Years 至 60 Years(Adult)
性别
All
接受健康志愿者
是

入选标准

  • •Age between 18-60 years
  • •Lean body weight >= 50 kg
  • •ASA physical status 1

排除标准

  • •Inability to cooperate with adequate airway assessment,
  • •History of hepatic, renal and coagulation diseases,
  • •Respiratory tract pathology
  • •Pregnancy
  • •Risk of regurgitation or aspiration
  • •Allergy to amide type of local anaesthetics
  • •No written informed consent by subject

研究组 & 干预措施

Interventional

Experimental

Subjects will be asked to inhale 4 ml lidocaine 4% via the Trachospray device

干预措施: Trachospray for awake videolaryngoscopy (Device)

结局指标

主要结局

Complete anaesthesia of the airway as evaluated with successful awake videolaryngoscopy with minimal discomfort for the subject

时间窗: 3 months

Discomfort and level of anesthesia will be measured with a numerical rating scale (NRS). 60 / 5.000 Vertaalresultaten So the result will be displayed in whole numbers.

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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