跳至主要内容
临床试验/ACTRN12608000414314
ACTRN12608000414314已完成4 期

A randomised clinical trial to compare the efficacy of pressurised vapocoolant spray and subcutaneous lignocaine injection in decreasing the pain of intravenous cannulation in the emergency department

Austin Health0 个研究点目标入组 220 人开始时间: 2008年8月22日最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
Austin Health
入组人数
220

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Prevention
盲法
Open (masking not used)

入排标准

年龄范围
18 Years 至 100 Years(—)
性别
All

入选标准

  • Emergency department patients, aged 18 years or more, requiring intravenous cannulation

排除标准

  • Refusal to provide consent
  • Inability to provide informed consent (Non-English speaking, altered mental state, significant illness, urgent need for IV cannulation)
  • Moderate to severe discomfort or pain
  • Diseases of the skin associated with cold intolerance (eg: Raynaud’s)
  • Known allergy to spray contents or lignocaine
  • Peripheral neuropathy
  • Parenteral analgesia in the previous 4 hours
  • Use of other local anaesthetics

研究者

发起方
Austin Health

相似试验