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临床试验/CTRI/2018/09/015673
CTRI/2018/09/015673招募中不适用

Comparison of levobupivacaine tramadol with levobupivacaine clonidine in caudal block in children undergoing infraumbilical surgery.

Jyoti1 个研究点 分布在 1 个国家目标入组 75 人开始时间: 2018年1月5日最近更新:

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
75
试验地点
1
主要终点
time duration of analgesia in the post operative period

研究概览

简要总结

The study will be comparing the effect of drug combinations given in caudal block analgesia for the post  operative pain relief in the patients. The patients will be children in the age group of 2 to 10 years who will be randomly allocated into 3 groups which will be receiving a particular combination of the drugs.  Group I - Levo Bupivacaine 0.25% 1 ml/kg , Group II - Levo Bupivacaine 0.25% 1ml/kg + tramadol 1mg/kg and Group III - Levo bupivacaine 1 ml/kg + Clonidine 1ug/kg after administration of general anaesthesia but before the start of surgery. Outcome will be measured as haemodynamic stability measured in terms of HR, MAP every 5, 10, 15, 30, 45, 60 and 90 mins intra operatively till the completion of the surgery and then duration of post operative analgesia in these patients measured with the help of CHIPPS score and Ramsay sedation score and also hemodynamic parameters at 1 hour interval till the 6th hour and then at 24 hours.

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
2.00 Year(s) 至 10.00 Year(s)(—)
性别
All

入选标准

  • children in ASA status 1 and 2 undergoing any type of surgical procedure in the lower abdominal region.

排除标准

  • ASA status 3,4 or 5 Any contraindication to caudal block such as scaral agenesis, tumors, local infection history of seizures hypersensitivity to any of the drugs in the study.

结局指标

主要结局

time duration of analgesia in the post operative period

时间窗: time duration of analgesia in the post operative period measured at 5, 10, 15,30,45,60,90 minutes

次要结局

  • hemodynamic stability in the intra operative period(5,10,15,30,45,60,90 intra operatively)

研究者

发起方
Jyoti
申办方类型
Other [self]

研究点 (1)

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