ACTRN12615000533594已完成4 期
Haemodynamic Effects Of Intravenous Paracetamol In Healthy Volunteers
Austin Hospital0 个研究点目标入组 24 人开始时间: 2015年5月27日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 24
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 60 Years（—）
- 性别
- All
入选标准
- •1. Adults (age >18 years but less than 60 years)
- •2. Healthy Volunteers
- •3. No regular medications
排除标准
- •Paracetamol use 24 hours prior to trial (in paracetamol only or in combination therapy)
- •Chronic renal impairment (Creatinine >120 umol/L)
- •Chronic liver disease (ALT >100IU/L)
- •Morbid obesity (BMI >35kg/m2)
- •Known allergic reaction to IV paracetamol, mannitol or normal saline
研究者
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