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临床试验/NCT02049970
NCT02049970已完成4 期

Effect of the Addition of Dexmedetomidine to Bupivacaine During Supraclavicular Brachial Plexus Blockade for Forearm Surgery.

TC Erciyes University1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2014年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
入组人数
44
试验地点
1
主要终点
the duration of sensorial block

研究概览

简要总结

the aim of this study was effect of the addition of dexmedetomidine to bupivacaine during supraclavicular brachial plexus blockade for forearm surgery, by low doses bupivacaine providing prolonged analgesia after surgery.

详细描述

Anaesthesia for surgeries to the upper extremity commonly is provided using brachial plexus anaesthesia.Various local anaesthetic mixtures can be used to prolong local anaesthesia duration and epinephrine , opioids and dexmedetomidine are frequently used for this purpose. this study was conducted to compare the effects of adding dexmedetomidine to local anaesthetics in the supraclavicular brachial plexus block by using nerve stimulators and ultrasonography guided. dexmedetomidine has also been found the prolong the duration of bupivacaine infraclavicular brachial plexus block.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 18-65 age
  • unwanted general anaesthesia
  • single forearm, arm surgery

排除标准

  • major psychiatric problems
  • major neurologic deficits
  • coagulopathy
  • drug allergies
  • chronic analgesic used

研究组 & 干预措施

dexmedetomidine and bupivacaine

Experimental

Bupivacaine 50 mg and dexmedetomidine 1 microgram/kg

干预措施: dexmedetomidine (Drug)

dexmedetomidine and bupivacaine

Experimental

Bupivacaine 50 mg and dexmedetomidine 1 microgram/kg

干预措施: bupivacaine (Drug)

Bupivacaine and placebo

Experimental

Bupivacaine 100 mg and SF 10 ml

干预措施: dexmedetomidine (Drug)

Bupivacaine and placebo

Experimental

Bupivacaine 100 mg and SF 10 ml

干预措施: bupivacaine (Drug)

结局指标

主要结局

the duration of sensorial block

时间窗: postoperative 1 day

pin-prick test

次要结局

  • the first time analgesic required(postoperative 1 day)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Recep Aksu

associate professor

TC Erciyes University

研究点 (1)

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