IRCT20141116019971N4已完成2 期
Evaluating the effectiveness of intravenous Propofol plus paracetamol versus paracetamol alone in benign headaches, a randomized placebo controlled clinical trial.
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 80
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 years 至 no limit(—)
- 性别
- All
入选标准
- •Age 18 years and above
- •Benign headaches
排除标准
- •Suspicious to secondary headaches based on the attending physician's judgment
- •Abnormal vital signs
- •Variation in the level of consciousness
- •Focal neurologic defficite
- •Allergy to the egg yolk, acetaminophen or propofol
- •Neck stiffness
- •Hepatic failure an chronic liver disease
研究者
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