ACTRN12617001559303已完成未知
Determining the feasibility of using patient controlled analgesia in emergency departments: A feasibility pilot randomised controlled trial
atasya Raja (PhD Candidate)0 个研究点目标入组 13 人开始时间: 2017年11月15日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 13
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
- Treatment
- 盲法
- Open (masking not used)
入排标准
- 年龄范围
- 18 Years 至 o limit（—）
- 性别
- All
入选标准
- •Patients presenting with severe abdominal pain with a numeric rating scale (NRS) greater than or equal to five out of ten and are likely to require an intravenous opioid
排除标准
- •<18 years old, not able to read and understand English, abnormal vital sign parameters, contraindications to using a PCA device, written informed consent not provided, known allergy to opiates, reduced level of consciousness evidenced by a Glasgow Coma Score <15, inability to operate a PCA device (e.g. decreased hand dexterity or visually impaired), inability to understand information about the study (e.g. dementia, learning difficulties, drug or alcohol intoxication, or acute confusion), history of chronic pain, history of tolerance or an addiction to opioids, history of chronic exposure to opioids (e. g. IV drug user, regional pain syndrome, or oncology related pain management), history of renal failure or insufficiency, inability to gain IV access, pregnant or breast feeding, clinical suspicion of opioid dependence or abuse, and opiate use in 24 hours before presentation to ED.
研究者
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