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临床试验/CTRI/2021/09/036202
CTRI/2021/09/036202尚未招募不适用

Effect of Lignocaine airway nebulisation vs intravenous lignocaine on intubation response in General anaesthesia patients. A Comparative Randomised clinical trial.

Pondicherry Institute of Medical Sciences1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2021年9月15日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
75
试验地点
1
主要终点
Primary objective: To compare hemodynamic responses to Intubation in topical

研究概览

简要总结

Effect of Lignocaine airway nebulisation vs intravenous lignocaine on intubation response in General Anaesthesia patients, a comparative randomised clinical trial.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Investigator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged between 18 and 60 yrs.
  • American Society of Anaesthesiologists ASA 1 and ASA 2 patients coming for GA.
  • Patients coming for elective procedures.

排除标准

  • Surgery involving the oral, nasopharyngeal, laryngotracheal airway or thyroid.
  • Patients history of respiratory disease (COPD, asthma).
  • History of recent respiratory tract infection.
  • Patients with anticipated difficult intubation and Those requiring > 3 attempts at laryngoscopy and intubation.
  • History of any known allergy to Lignocaine.
  • Patients coming for emergency procedures.

结局指标

主要结局

Primary objective: To compare hemodynamic responses to Intubation in topical

时间窗: Baseline, 1min, 2min, 3min, 4min, 5min, 10min.

2% lignocaine and 4% lignocaine patients and compare it with intravenous lignocaine

时间窗: Baseline, 1min, 2min, 3min, 4min, 5min, 10min.

in patients undergoing General anaesthesia.

时间窗: Baseline, 1min, 2min, 3min, 4min, 5min, 10min.

次要结局

  • To study any adverse drug reactions(1min, 2min, 3min, 4min, 5min, 10min)

研究者

申办方类型
Research institution and hospital

研究点 (1)

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