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临床试验/TCTR20160525001
TCTR20160525001已完成2 期

A Randomized Comparison Between Conventional and Costoclavicular Ultrasound-Guided Infraclavicular Blocks

one0 个研究点目标入组 90 人开始时间: 2016年5月25日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
one
入组人数
90

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
18 Years 至 75 Years(—)
性别
All

入选标准

  • - Patients undergoing upper extremity surgery (elbow and below).
  • - American Society of Anesthesiologists classification 1-3
  • - Body mass index between 18 and 30 kg/m2

排除标准

  • - pre existing neuropathy or coagulopathy
  • - renal failure or hepatic failure
  • - allergy to local anesthetics
  • - pregnancy
  • - prior surgery in the area of the infraclavicular fossa
  • - chronic pain syndromes requiring opioid intake at home

研究者

发起方
one

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