跳至主要内容
临床试验/CTRI/2019/02/017870
CTRI/2019/02/017870尚未招募不适用

Efficacy of Fentanyl vs Clonidine as an adjuvant to Ropivacaine compared to Ropivacaine for postoperative analgesia in caudal block for infraumbilical surgeries: A Prospective double blinded randomized control study

Balu Sankar J1 个研究点 分布在 1 个国家目标入组 72 人开始时间: 2019年5月3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
72
试验地点
1
主要终点
To study the duration of analgesia in terms of pain score and total analgesic requirement.

研究概览

简要总结

This is a prospective double blinded randomised control study to compare the efficacy of fentanyl and clonidine as an adjuvant to ropivacaine and with ropivacaine alone in caudal block for 72 pediatric patients posted for infraumbilical surgeries. The primary outcome is to study the duration of analgesia in terms of pain score and total analgesic requirements. The secondary objectives are to study the level of sedation, hemodynamic changes, incidence of nausea, vomiting and pruritis.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant and Outcome Assessor Blinded

入排标准

年龄范围
2.00 Year(s) 至 8.00 Year(s)(—)
性别
All

入选标准

  • ASA PS 1 and 2 Weight between 10 and 30 Kilograms.

排除标准

  • Refusal for caudal block ASA 3 and above physical status Allergic to local anaesthetics and adjuvants Children less than 2 years of age Infection at block site Bleeding diasthesis, pre-existing neurological, spinal diseases, mental retardation, neuromuscular disorders.

结局指标

主要结局

To study the duration of analgesia in terms of pain score and total analgesic requirement.

时间窗: Post Operative Period

次要结局

  • To study sedation, hemodynamic changes, incidence of nausea, vomiting and pruritis(Intraoperative and post operative period.)

研究者

发起方
Balu Sankar J
申办方类型
Other [Principal Investigator]

研究点 (1)

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