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临床试验/NCT01334619
NCT01334619已完成4 期

Ropivacaine Volume for Ultrasound-guided Retrograde Infraclavicular Brachial Plexus Block

Beijing Jishuitan Hospital2 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2010年3月最近更新:
适应症

试验速览

阶段
4 期
状态
已完成
入组人数
30
试验地点
2
主要终点
VAS of brachial plexus innervated area

研究概览

简要总结

The retrograde infraclavicular brachial plexus block has been proved an effective and safe approach. Realtime ultrasound guide will facilitate a successful peripheral nerve block. The purpose of this study was to determine the medium effective volume required to produce an effective retrograde infraclavicular block using an ultrasound (US)-guided technique.

详细描述

Thirty adults undergoing elective upper limb surgery received an US-guided retrograde infraclavicular block. The initial concentration of 0.5% ropivacaine injected was 30 ml, which was subsequently varied at a ratio of 1: 1.2 for each consecutive patient according to the response of the previous patient. The medium effective volume (EV50) was determined using the Dixon and Massey up-and-down method. The effective volume in 95% of patients (EV95) was calculated using probit regression.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
Single (Participant)

入排标准

年龄范围
18 Years 至 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elected upper extremity operations
  • BMI 17~30kg/m2

排除标准

  • Infection at injection site
  • Coagulation Dysfunction
  • Phrenic nerve palsy
  • Pneumothorax
  • Recurrent laryngeal nerve palsy
  • Clavicle fracture combined with nerve damage

结局指标

主要结局

VAS of brachial plexus innervated area

时间窗: 20 minutes

effect and side effects of the present block approach for brachial plexus.

次要结局

  • medium effective ropivacaine volume(about 2 months)

研究者

申办方类型
Other

研究点 (2)

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