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临床试验/ISRCTN85118989
ISRCTN85118989已完成不适用

Efficacy of short course high-dose amoxicillin in the treatment of non-severe community acquired-pneumonia in children: A double-blind, randomised controlled trial

Medical Research Council Laboratories (Gambia)0 个研究点目标入组 905 人开始时间: 2010年6月3日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
905

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. Aged 2 to 59 months
  • 2. Either sex
  • 3. Nutritional status: Weight-for-height > 70% of National Center for Health Statistics (NCHS) reference without oedema
  • 4. Non-severe pneumonia according to WHO definition: if the child has fast breathing with cough or difficult breathing and there is no chest indrawing or other danger signs

排除标准

  • 1. Having severe pneumonia or very sever disease or if needs oxygen
  • 2. Needed antibiotic, steroid, theophylline or digitalis for treatment of any other condition
  • 3. Had been enrolled in the trial for an earlier episode of pneumonia
  • 4. Was admitted in a hospital in the previous month
  • 5. History of hypersensitivity or intolerance to amoxicillin or co-trimoxazole
  • 6. History of receiving any antibiotic within last 48 hours, this was be confirmed from health cards or village health workers
  • 7. A history of three or more episodes of wheeze, acute bronchial asthma
  • 8. Evidence of underlying haematologic, renal, hepatic or cardiovascular disease
  • 9. Chronic steroid use or concomitant treatment with theophylline or digitalis glycosides
  • 10. Living outside the study area

研究者

发起方
Medical Research Council Laboratories (Gambia)

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