跳至主要内容
临床试验/CTRI/2023/08/056787
CTRI/2023/08/056787尚未招募4 期

A Comparative study of levobupivacaine 0.25% with dexmeditomidine and dexamethasone as adjuvant in caudal block for paediatric patients undergoing infraumbilical surgeries.

DR Batula Shravani1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2023年1月9日最近更新:

试验速览

阶段
4 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
Its Expected that moderate dose of caudal analgesia with 0.25% levobupivacaine 1ml/kg with dexmeditomidine is more effective than 0.25% levobupivacaine 1ml/kg with dexamethasone

研究概览

简要总结

This study is a Prospective double blind randomised control study comparing evaluation of 0.25% levobupivacaine with Dexmeditomidine 1ug/kg and 0.25% Levobupivacaine with 1mg/kg dexamethasone in Caudal block in Children undergoing infraumbilical surgeries ,in this study we are comparing postoperative analgesic effect of both the drugs.

研究设计

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

入排标准

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

入选标准

  • Patients undergoing infraumbilical surgeries Parents or guardian giving consent to participate in study of age between 1year to 8years of ASA Grade I and II.

排除标准

  • Patients guardian not giving consent to participate in the study ASA Grade III and IV Patients with known hypersenstivity to local anaesthestics Abnormal coagulopathy Preexisting neurological disease Local sepsis or infection Mentally retarded child Abnormal sacral anatomy.

结局指标

主要结局

Its Expected that moderate dose of caudal analgesia with 0.25% levobupivacaine 1ml/kg with dexmeditomidine is more effective than 0.25% levobupivacaine 1ml/kg with dexamethasone

时间窗: 24hours

次要结局

未报告次要终点

研究者

发起方
DR Batula Shravani
申办方类型
Other [self]

研究点 (1)

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