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临床试验/PACTR201411000937373
PACTR201411000937373招募中未知

A trial of the safety of low dose primaquine in addition to ACTs commonly used in Senegal.

niversity Cheikh Anta DIOP of Dakar, Department of Medical Parasitology.0 个研究点目标入组 300 人开始时间: 2014年11月10日最近更新:
适应症

试验速览

阶段
未知
状态
招募中
发起方
入组人数
300

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
20 Year(s) 至 50 Year(s)(—)
性别
All

入选标准

  • 1. Adult patients with acute uncomplicated P. falciparum malaria;
  • 2. P. falciparum monospecific infection with parasite density ranged from 1000 to 100 000 trophozoite/¿L.
  • 3. Willingness to participate in the planed study investigations and to remain in the study area for the duration of the study;
  • 4. Participants informed consent;
  • 5. Absence of known chronic illness such as hypertension, diabetes, renal and liver disease.

排除标准

  • 1. Known allergy to the study medications;
  • 2. Presence of severe anaemia (haemoglobin < 8 g/dl) at enrolment;
  • 3. Pregnancy, or breastfeeding.

研究者

发起方
niversity Cheikh Anta DIOP of Dakar, Department of Medical Parasitology.

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