PACTR201110000321348已完成未知
INTRAVENOUS ARTESUNATE PLUS ACT Vs INTRAVENOUS QUININE PLUS ACT FOR SEVERE MALARIA TREATMENT IN UGANDAN PATIENTS
INFECTIOUS DISEASES INSTITUTE LTD0 个研究点目标入组 404 人开始时间: 2011年10月4日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 404
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
- 6 Month(s) 至 60 Year(s)（—）
- 性别
- All
入选标准
- •1) Age 6 months and above
- •2) With a positive blood smear for P. falciparum asexual parasitaemia with no other cause of the symptoms
- •3) Who meet the WHO clinical or laboratory criteria for severe malaria requiring parenteral therapy
- •3) Whose parents/caretakers provide written informed consent and are willing to participate in 42 day follow up
排除标准
- •1) Administration of any additional antimalarial drugs that are not study drugs within 72 hours before study enrolment and during the course of the study.
- •2) Emergence of any non-malarial febrile illness which may interfere with the classification of malaria treatment outcome
- •3) Movement away from the study area interfering with follow-up assessment
- •4) Patients with contraindications to taking the study drugs
- •5) Withdrawal of consent
研究者
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