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临床试验/IRCT20140211016554N4
IRCT20140211016554N4已完成2 期

Evaluation of the effectiveness of oral dapsone with intralesional antimoniate in treatment of cutaneous leishmaniasis in comparison with intralesional antimoniate alone

Mashhad University of Medical Sciences0 个研究点目标入组 100 人开始时间: 待定最近更新:
适应症

试验速览

阶段
2 期
状态
已完成
入组人数
100

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
10 years 至 40 years(—)
性别
All

入选标准

  • positive direct smear of the lesion in terms of leishman bodies
  • patient has indication of topical treatment according to the physician
  • less than six month has elapsed since the manifestation of lesion
  • patient has not received any previous treatment for cutaneous leishmaniasis
  • intervention group has normal values for CBC;G6PD;LFT
  • location of lesion is either on upper limbs or face

排除标准

  • sensitivity to glucantime (severe topical reaction, anaphylaxis).
  • absence of regular follow-ups
  • existence of secondary infection in lesion
  • use of other treatments during the study
  • dapsone side effects including methemoglobinemia, hemolytic anemia, agranulocytosis, peripheral neuropathy, hypersensitivity

研究者

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