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临床试验/CTRI/2026/02/102959
CTRI/2026/02/102959尚未招募不适用

A comparison of nebulised lidocaine versus dexmedetomidine for attenuation of hemodynamic response to laryngoscopy and tracheal intubation.

BJ medical college and Civil hospital Ahmedabad1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2026年2月20日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
60
试验地点
1

研究概览

简要总结

Direct laryngoscopy and tracheal intubation following induction of anaesthesia are associated with hemodynamic changes due to increased sympatho-adrenal activity, which may result in increase in heart rate and blood pressure. This rise in blood pressure and heart rate is transient and variable. This response is likely to be tolerated by healthy patients but can be exaggerated in susceptible individuals and may precipitate hypertensive crises, myocardial ischemia, arrhythmias, or increases in intracranial pressure.

Lidocaine is a local anaesthetic and class 1B antiarrhythmic drug which can provide topical analgesia by blocking nerve conduction and diminish airway reflex. Nebulised Lidocaine(2%)  administered in doses of 2mg/kg is found to be effective to attenuate hemodynamic response after laryngoscopy and tracheal intubation.

Dexmedetomidine is a potent and highly selective alpha-2 receptor agonist with sympatholytic, sedative, amnestic and analgesic properties. Nebulised dexmedetomidine administered in doses of 1µg/kg is found to be an effective premedication to attenuate hemodynamic response after laryngoscopy and tracheal intubation**.**

This study is designed to compare the effect of nebulised Lidocaine versus Dexmedetomidine for attenuation of  hemodynamic response to laryngoscopy and tracheal intubation**.**

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant 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 of ASA 1,2,3 undergoing any surgery under general anaesthesia requiring endotracheal intubation Patients with normal airway anatomy Non smokers.

排除标准

  • Patients with allergy to study medications Patients with pregnancy and lactation Patients with BMI more than 30 ASA 4,5 Patients who will give negative consent.

研究者

发起方
BJ medical college and Civil hospital Ahmedabad
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Hetalba R Jadeja

BJ Medical College, Ahmedabad.

研究点 (1)

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