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临床试验/NCT06327867
NCT06327867尚未招募不适用

Comparison of Video Laryngoscopy Versus Direct Laryngoscopy for Orotracheal Intubation Among Adults in Emergency Department

Patan Academy of Health Sciences0 个研究点目标入组 126 人开始时间: 2024年5月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
126
主要终点
First pass success of video laryngoscopy in oro tracheal intubation

研究概览

简要总结

This is an open-label, single center, prospective, randomized, comparative, intervention study.

The goal of this study is to compare the success rate of video laryngoscopy vs direct laryngoscopy for first pass oro tracheal intubation. The other question it aims to answer are:

  1. To assess the adverse events during video laryngoscopy
  2. To assess the adverse events during direct Laryngoscopy
  3. To compare the first pass success rate of DL vs VL according to demographic profile (age and sex)

详细描述

All consecutive patients presenting in Emergency medicine room requiring intubation, will be recruited in this study after taking informed written consent from the patients' family, excluding those falling in exclusion criteria. Direct laryngoscopy will be done by Mackintosh Laryngoscope with blade no 3 or 4. Video Laryngoscopy will be done by Mcgrath Mac Video Laryngoscope in respective groups. Intubations will be done by ER physicians and Emergency fellows of Emergency department. The total number of required sample size will be calculated and the obtained number will be divided in a group of 21 with block of 6 each. After randomizing the group and the block from a computerized software, a total of 21 envelope will be prepared in a consecutive manner and the patient will be intubated as per the pre decided blocks. All the patients in emergency who require intubation and falling into the inclusion criteria will be assessed. Informed written consent will be taken from the patient's family explaining that they will be a part of study and either of the laryngoscopy method will be used in them. Informed consent will be taken by one of the investigators, (ER physicians and emergency medicine fellow) who will be performing intubations in them.Inclusion criteria-

  • Age 18 years
  • Patient requiring orotracheal intubation
  • Those who give written informed consent

Exclusion criteria-

  • Pregnancy
  • Intubations done by medical officers

Randomization-

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

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

  • Age 18 years
  • Patient requiring orotracheal intubation
  • Those who give written informed consent

排除标准

  • Intubations done by medical officers

结局指标

主要结局

First pass success of video laryngoscopy in oro tracheal intubation

时间窗: 1 year

success of oro tracheal intubation during VL

First pass success of direct laryngoscopy in oro tracheal intubation

时间窗: 1 year

success of oro tracheal intubation during DL

次要结局

  • Better visualization of Cormack-Lehane grading between two methods(1 year)
  • Complications rates between two methods.(1 year)
  • Use of alternative methods for ventilation or oxygenation between two methods(1 year)

研究者

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

Rony Maharjan

Doctor, Lecturer, Department of General practice and Emergency medicine, Priniciple Investigator

Patan Academy of Health Sciences

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