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临床试验/ISRCTN27232551
ISRCTN27232551已完成不适用

evamisole hydrochloride as adjunctive therapy in severe falciparum malaria with high parasitaemia

niversity of Oxford (United Kingdom)0 个研究点目标入组 60 人开始时间: 2006年5月24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
60

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

  • Current information as of 29/07/2010:
  • 1. The patient or attending relative, able and willing to give informed consent. The proposed consent form and information sheets are attached and will be translated into the local language.
  • 2. Severe falciparum malaria
  • 3. Peripheral blood parasitaemia more than or equal to 2%
  • 4. Patients aged 16 to 65 years old, both genders
  • 5. No contraindications to levamisole, or artesunate therapy, such as documented allergies to either of the drugs
  • Initial information at time of registration:
  • 1. The patient or attending relative, able and willing to give informed consent. The proposed consent form and information sheets are attached and will be translated into the local language.
  • 2. Severe falciparum malaria
  • 3. Peripheral blood parasitaemia more than or equal to 5%
  • 4. Patients aged 16 to 65 years old, both genders
  • 5. No contraindications to levamisole, or artesunate therapy, such as documented allergies to either of the drugs

排除标准

  • Current information as of 29/07/2010:
  • 1. Patient or relatives unable or unwilling to give informed consent
  • 2. More than one dose of previous antimalarial treatment within one week of admission
  • 3. Pregnancy or breastfeeding
  • Initial information at time of registration:
  • 1. Patient or relatives unable or unwilling to give informed consent
  • 2. Previous antimalarial treatment within one week of admission
  • 3. Pregnancy

研究者

发起方
niversity of Oxford (United Kingdom)

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