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
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
Aikta Gupta
Chacha Nehru Bal Chikitsalaya, Geeta Colony, Delhi
