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临床试验/TCTR20150624001
TCTR20150624001已完成2 期

A Randomized Comparison Between Intravenous and Perineural Dexamethasone for Ultrasound-Guided Infraclavicular Blocks

o sponsor0 个研究点目标入组 150 人开始时间: 2015年6月24日最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
发起方
入组人数
150

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) with
  • - American Society of Anesthesiologists classification 1-3
  • - body mass index between 18 and 35

排除标准

  • - adults who are unable to give their own consent
  • -pre-existing neuropathy (assessed by history and physical examination)
  • -coagulopathy (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. platelets ≤ 100, or International Normalized Ratio ≥ 1.4)
  • -renal failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. creatinine ≥ 100)
  • -hepatic failure (assessed by history and physical examination and, if deemed clinically necessary, by blood work up i.e. transaminases ≥ 100)
  • -allergy to local anesthetics (LAs)
  • -pregnancy
  • -prior surgery in the infraclavicular region
  • - chronic pain syndromes requiring opioid intake at home

研究者

发起方
o sponsor

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