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临床试验/CTRI/2012/12/003188
CTRI/2012/12/003188已完成4 期

Evaluation of Pharmacokinetics of anti-malarial drugs in children

Research society0 个研究点目标入组 49 人开始时间: 待定最近更新:

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
49

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

入选标准

  • 1.children below 12 years of age
  • 2.children of either gender
  • 3.children with confirmed cases of p.vivax malaria on microscopy by thick and thin smears
  • 4.children with fever, chills, nausea, vomiting, headache, malaise, and not having signs/symptoms of severe malaria.
  • 5.Willing to Consent & participate in the study.
  • 6.normal G6PD status as assessed by qualitative and quantitative tests.

排除标准

  • 1.children with G6PD deficiency
  • 2.Known hypersensitivity to Chloroquine, primaquine or related drugs (e.g., iodoquinol) as assessed by history.
  • 3.Persons receiving treatment with other potentially hemolytic drugs.
  • 4.Any clinically significant diseases(hepatic, cardiac or pulmonary or subjects with acute nephritic syndrome)
  • 5.History of autoimmune disease or acute or chronic bronchospastic disease (including asthma and COPD, treated or not treated) or clinically significant drug allergy; history of atopic allergy (asthma, urticaria, eczematous dermatitis)
  • 6.history of taking any anti-malarial drugs within last one month.
  • 7.children with severe or complicated malaria or mixed malarial infections.

研究者

发起方
Research society

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