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
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 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
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