CTRI/2020/01/022653尚未招募不适用
A Prospective Randomised Study Comparing ErectorSpinae Plane Block with Caudal Block For Intra and Postoperative Analgesia in Pediatric Laparoscopic Surgeries.
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- Primary objective is to demonstrate persistence of
研究概览
简要总结
A prospective randomised study comparing erector
spinae plane block with caudal block for intraoperative and post
operative analgesia in pediatric laparoscopic surgeries
The aim of this study is to compare the analgesic effect of ESP block and Caudal block in laparoscopic surgery.
OBJECTIVES:
- Primary objective is to demonstrate persistence of analgesia for upto 6 hours.
- Secondary objective is to measure the intraoperative hemodynamic stability and time to first use of rescue analgesic.
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 1.00 Year(s) 至 6.00 Year(s)（—）
- 性别
- All
入选标准
- •Informed consent from parents ASA 1 & 2 Age group 1-6 years undergoing laparoscopic surgery Elective surgeries.
排除标准
- •Children with hypersensitivity to study drugs Suspected coagulopathy Skeletal deformity Infection at injection site History of developmental delay / neurological diseases.
结局指标
主要结局
Primary objective is to demonstrate persistence of
时间窗: 1 hour ,2 hour,3 hour, 4 hour, and 6 hour
analgesia for upto 6 hours.
时间窗: 1 hour ,2 hour,3 hour, 4 hour, and 6 hour
次要结局
- Secondary objective is to measure the(intraoperative hemodynamic stability and time to)
研究者
研究点 (1)
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