ACTRN12615000481572已完成3 期
A prospective, double-blind, double-dummy, randomised controlled trial to compare pain relief from intravenous paracetamol and oral paracetamol in acute pain patients presenting to the Emergency Department
The Townsville Hospital and Health Service0 个研究点目标入组 100 人开始时间: 2015年5月15日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 100
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 o limit（—）
- 性别
- All
入选标准
- •Age greater than or equal to 18years
- •Already has intravenous access or has a clinical condition indicating that intravenous access is required
- •Have received at least one initial dose of morphine (either with Queensland Ambulance Service or in ED) with ongoing pain score >40mm on the Visual Analogue Scale (VAS) at > 5 minutes post administration of morphine or equivalent.
排除标准
- •Any state (e.g. intoxicated) or medical history (e.g. mental health disorder) impairing accurate pain assessment
- •Known/suspected to have drug dependence
- •Allergic to paracetamol
- •Received or taken paracetamol in the last 6 hours
- •Known or suspected Renal or hepatic insufficiency
- •Currently enrolled in other clinical trials for the treatment of pain
- •Unable to safely swallow oral medication
研究者
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