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临床试验/CTRI/2021/10/037274
CTRI/2021/10/037274尚未招募不适用

A PROSPECTIVE RANDOMIZED, COMPARITIVE STUDY BETWEEN DEXMEDETOMEDINE AND BUPRENORPHINE AS AN ADJUVANT TO ROPIVACAINE 0.5% IN ULTRASOUND GUIDED SUPRACLAVICULAR BRACHIAL PLEXUS BLOCK FOR UPPER LIMB ORTHOPEDIC SURGERIES

Sanjay Gandhi Institute Of Trauma And Orthopedics1 个研究点 分布在 1 个国家目标入组 90 人开始时间: 2021年10月21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
90
试验地点
1
主要终点
time of onset of sensory block and duration of analgesia

研究概览

简要总结

.Supraclavicular block is a regional anaesthetic technique used as an alternative or adjunct to general anesthesia or used for postoperative pain control for upper extremity surgeries (mid-humerus through the hand).

Various adjuvants have been added to local anesthetics to increase the efficacy and duration of blocks,minimizing systemic adverse effects along with a reduction in the total dose of local anesthetic used.

Dexmedetomidine, a potent α2 adrenocepter agonist ,has been reported to improve the quality of intrathecal and epidural anesthesia.(1,2,3) Its use in peripheral nerve blocks has recently been described.

Buprenorphine is lipophilic opioid with high molecular weight and having high affinity for μ receptors, has a longer duration of action,and is easily available, cost-effective and hence selected for this study

Ropivacaine has a long duration of action, with similar pharmacology to bupivacaine but a wider safety margin

In this study, we will investigate whether adding dexmedetomidine  or buprenorphine to 0.5%ropivacaine for supraclavicular brachial plexus block would affect the sensory and motor blocks and duration of analgesia

研究设计

研究类型
Interventional
分配方式
Random Number Table
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Patients aged between 18 to 60 years admitted for elective upperlimb orthopaedic surgeries in Sanjay Gandhi Institute Of Trauma And Orthopaedics,Bengaluru.

排除标准

  • History of neurological, psychiatric, neuromuscular,alcoholism or drug abuse and patients receiving adrenoceptor agonist or antagonist therapy.

结局指标

主要结局

time of onset of sensory block and duration of analgesia

时间窗: 1 day

次要结局

  • any adverse effects(1 day)

研究者

发起方
Sanjay Gandhi Institute Of Trauma And Orthopedics
申办方类型
Government medical college

研究点 (1)

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