NCT02711241终止3 期
Optimal Analgesia in Acute Gastroenteritis in Emergency Department Setting: Dipyrone Versus Papaverine
适应症
干预措施
相关药物
试验速览
- 阶段
- 3 期
- 状态
- 终止
- 入组人数
- 15
- 试验地点
- 1
- 主要终点
- Change in pain assessment (VAS) as opposed the pain assessment on admission
研究概览
简要总结
The purpose of this study is to find out an optimal way of analgesia in case of acute infectious gastroenteritis the investigators are going to compare two medicines that are used on everyday basis (without being ever before subject to scientifical study): Dipyrone and papaverine The study is done in the Emergency Department setting. Thus, only first 6 hours of treatment is included in study
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •acute gastroenteritis
- •VAS scale of pain perception at least 4
排除标准
- •pregnancy
- •allergy to any one of study preparations
- •blood pressure less than 85 on admission
- •surgical condition (acute abdomen) suspected or diagnosed
研究组 & 干预措施
Dipyrone
Active Comparator
干预措施: Dipyrone (Drug)
Papaverine
Active Comparator
干预措施: Papaverine (Drug)
结局指标
主要结局
Change in pain assessment (VAS) as opposed the pain assessment on admission
时间窗: 30 min, 1 hour, 2 hours, on discharge (up to 24 hours)
次要结局
- Need for second analgesic medicine(24 hours)
研究者
STALNIKOWICZ-DARVASI RUTH
Professsor
Hadassah Medical Organization
研究点 (1)
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