ISRCTN11886401已完成不适用
A randomised controlled trial of rectal versus oral acetaminophen antipyresis in childre
American University of Beirut (Lebanon)0 个研究点目标入组 48 人开始时间: 2005年3月10日最近更新:
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- 入组人数
- 48
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
- 性别
- All
入选标准
- •1. Age between 6 months and 13 years
- •2. Rectal temperature greater than or equal to 38.5 °C
- •3. Consent of treating physician
- •4. Written consent of parent and oral consent of child if older than 10 years
- •5. No antipyretic intake for 8 hours prior to enrolment
排除标准
- •1. Presence of concurrent or previous hepatic disease
- •2. Chronic and/or serious disease such as malignancy, septic shock, malabsorption syndromes etc.
- •3. Any condition interfering with the absorption of oral or rectal acetaminophen such as vomiting or severe diarrhoea, ileus, rectal bleeding etc.
- •4. Hypersensitivity to acetaminophen
研究者
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