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临床试验/NCT01737437
NCT01737437Unknown不适用

Effect of Lidocaine Sprayed on Direct Laryngoscopy and Trachea on Hemodynamics During Endotracheal Intubation

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2012年10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
80
试验地点
1
主要终点
mean blood pressure, heart rate

研究概览

简要总结

A previous study demonstrated topical lidocaine spray on the larynx and the trachea is effective in reducing hemodynamic response to laryngoscopy and endotracheal intubation. In clinical practice, blind oropharyngeal application of lidocaine without aiding direct laryngoscopy can not assured that sprayed lidocaine effectively reaches the larynx and trachea. Therefore, direct laryngoscopy should be necessary to reach topical lidocaine to correct sites. Unfortunately, direct laryngoscopy itself can affect hemodynamics during spraying lidocaine. In this study, we will investigate an effect of lidocaine sprayed on direct laryngoscopy and the tracheal mucosa on hemodynamic change throughout intubation.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • aged 20-60 years,
  • ASA groups I or II

排除标准

  • ASA III or IV,
  • hypertension,
  • anticipated difficult airway, and
  • severe coronary and cerebrovascular diseases

研究组 & 干预措施

group L

Experimental

10% Lidocaine was applied to the laryngoscope blade and 0.9% normal saline was applied to the trachea.

干预措施: group L (Drug)

group C

Placebo Comparator

0.9% normal saline was applied to trachea and laryngoscope blade in Group C.

干预措施: group C (Drug)

group V

Experimental

0.9% normal saline was applied to the laryngoscope blade and 10% Lidocaine was applied on trachea.

干预措施: group V (Drug)

group LV

Experimental

10% Lidocaine was applied on laryngoscope blade and trachea.

干预措施: group LV (Drug)

结局指标

主要结局

mean blood pressure, heart rate

时间窗: baseline, at laryngoscope insertion, 60s after laryngoscope insertion, during intubation, one, two, three min after endotracheal intubation

次要结局

未报告次要终点

研究者

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

Hee-Pyoung Park

Professor

Seoul National University Hospital

研究点 (1)

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