ACTRN12615001151527终止3 期
Double blind randomised controlled study to compare the usual practice of additional opiates with iv ketamine in unselected emergency patients complaining of moderate to severe pain despite already receiving opiate analgesia.
Bundaberg Base Hospital0 个研究点目标入组 23 人开始时间: 2015年10月29日最近更新:
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 发起方
- 入组人数
- 23
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
- Blinded (masking used)
入排标准
- 年龄范围
- 18 Years 至 95 Years（—）
- 性别
- All
入选标准
- •Patients reporting acute onset of pain of any cause except cardiac origin but including cases where the cause is unknown. A verbal numeric rating scale pain score of greater than or equal to 5 after having received a total intravenous dose of 7.5mg morphine, 100mcg fentanyl or other equipotent opiate.
排除标准
- •Patients whose primary language is other than English
- •Women who are pregnant
- •Patients aged <18 years
- •Patients with intellectual or mental impairment
- •A patient in whom we are unable to gain venous access
- •Patients with known chronic kidney disease stage 4 or above
- •Acute severe respiratory distress
- •Presenting with presumed cardiac diagnosis
- •A documented allergy to morphine or ketamine
研究者
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