跳至主要内容
临床试验/CTRI/2014/08/004822
CTRI/2014/08/004822已完成不适用

Comparison of Ultrasound-Guided Supraclavicular, Infraclavicular and Interscalene Brachial Plexus Blocks for Upper Limb Surgery: A Randomised, Observer-Blinded Study.

Post Graduate Institute of Medical Education and Research1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2012年7月19日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
60
试验地点
1
主要终点
the block onset time

研究概览

简要总结

This trial was conducted to compare the ease of performance and effectiveness of ultrasound guided supraclavicular, infraclavicular and interscalene techniques of bracheal plexus block for upper arm and forearm surgery. Sixty adult patients of ASA grade I-III undergoing upper limb surgery were randomly allocated into 3 groups to receive ultrasound-guided supraclavicular, infraclavicular and interscalene blocks.The imaging times and block performance times were comparable among groups. Though, the onset time was longer in interscalene group as compared to other groups, no difference was observed in the success rate, duration of analgesia and adverse effects. We concluded that ultrasound guided interscalene block can be performed as rapidly as supraclavicular and infraclavicular blocks and results in similar success rate for upper limb surgery.

研究设计

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

  • Sixty patients of ASA physical status of I-III, undergoing upper arm and forearm surgery.

排除标准

  • Patients with clinically significant coagulopathy, morbid obesity (body mass index>40), infection at the injection site, allergy to local anaesthetics, mental incapacity or language barrier precluding assessment were excluded.

结局指标

主要结局

the block onset time

时间窗: The sensory and motor blockade were assessed every 5 min intervals till complete or maximum sensory and motor blockade was achieved

次要结局

  • the duration of analgesia and safety(Postoperative period)

研究者

发起方
Post Graduate Institute of Medical Education and Research
申办方类型
Research institution and hospital

研究点 (1)

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