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临床试验/CTRI/2026/01/101816
CTRI/2026/01/101816尚未招募不适用

Comparative Evaluation On Efficacy And Safety Of Two Different Doses Of Intravenous Dexmedetomidine On Postoperative Emergence Delirium In Paediatric Patients Undergoing Eye Surgery- A Randomised Controlled Trial

Chacha Nehru Bal Chikitsalaya1 个研究点 分布在 1 个国家目标入组 105 人开始时间: 2026年2月4日最近更新:

试验速览

阶段
不适用
状态
尚未招募
入组人数
105
试验地点
1

研究概览

简要总结

It is a prospective, randomised study comparing efficacy and safety of two different doses of intravenous dexmedetomidine versus placebo (normal saline) given prior to end of surgery to reduce incidence of Emergence delirium in paediatric patients undergoing eye surgery. Extubation time, severity of emergence delirium, postoperative pain, sedation level, adverse effects and haemodynamic parameters in immediate postopeartive period will also be monitored. Study will be conducted at Department of Anaesthesia at Chacha Nehru Bal Chikitsalaya. Study will include children between 2 to 10 years of age undergoing elective unilateral eye surgery belonging to ASA I and II. It will include 105 children within a course of one year after the initiation of study.

研究设计

研究类型
Interventional
分配方式
Randomized
盲法
Participant and Investigator Blinded

入排标准

年龄范围
2.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • ASA grade I-II for elective unilateral eye surgery.

排除标准

  • History of developmental delay, neurological or psychiatric disorder, heart diseases like cardiac arrhythmia, significant bradycardia, conduction block.

研究者

申办方类型
Research institution and hospital
责任方
Principal Investigator
主要研究者

Aikta Gupta

Chacha Nehru Bal Chikitsalaya, Geeta Colony, Delhi

研究点 (1)

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