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临床试验/CTRI/2022/03/041349
CTRI/2022/03/041349尚未招募3 期

Comparison of Dexmedetomidine and Clonidine as an adjuvant to Bupivacaine 0.25% in supraclavicular brachial plexus block under ultrasound guidance : A prospective randomised double blind study Â

sanjay gandhi institute of trauma and orthopaedics1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2022年4月15日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
60
试验地点
1
主要终点
To study duration of analgesia and time to request of rescue analgesia in first 24hours post surgery

研究概览

简要总结

.Regional anesthesia is the most used procedure for upper limb surgeries.

•Ultrasound guided  supraclavicular approach for the brachial plexus block is preferred, as they produce ideal  operating conditions with fewer complications

•Apart from local anesthetic agents, multiple  other drugs were used as adjuvants.

•In the recent past, both dexmedetomidine and clonidine were extensively studied as an adjuvant agent.

•Alpha 2A receptor specificity of dexmedetomidine over clonidine was quoted to be  one of the reasons for better efficacy over clonidine.

•In this study, we will compare dexmedetomidine with clonidine as an adjuvant in upper limb surgeries.

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
18.00 Year(s) 至 65.00 Year(s)(—)
性别
All

入选标准

  • ASA physical status I and II patients of either sex Aged between 18 to 65 years and normal BMI Elective upper limb orthopaedic surgeries.

排除标准

  • Patients with severe medical comorbidities and local site infection Patients receiving adrenoceptor agonist or antagonist therapy.

结局指标

主要结局

To study duration of analgesia and time to request of rescue analgesia in first 24hours post surgery

时间窗: first 30 minutes post surgery and then every 2nd hourly till patient requests for rescue analgesia

次要结局

  • Time Of Onset And Duration Of Sensory And Motor Blockade and Any other Side Effects

研究者

发起方
sanjay gandhi institute of trauma and orthopaedics
申办方类型
Government medical college

研究点 (1)

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