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临床试验/ISRCTN77659407
ISRCTN77659407已完成不适用

Comparison of combination of imiquimod and glucantime with glucantime alone in treatment of acute anthroponotic cutaneous leishmaniasis

World Health Organisation - Eastern Mediterranean Regional Office (EMRO) (Egypt)0 个研究点目标入组 120 人开始时间: 2005年4月19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
120

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

  • 1. Patients with anthroponotic cutaneous leishmaniasis caused by leishmania tropica
  • 2. Aged 12 to 60 years
  • 3. With less than 5 lesions each less than 5 cm in greatest diameter and duration less than 6 months

排除标准

  • 1. Pregnant or lactating women
  • 2. Duration of lesions more than 6 months
  • 3. Number of lesions more than 5
  • 4. Lesions greater than 5 cm in their largest diameter
  • 5. History of any full course of standard treatment (antimonials)
  • 6. History of allergy to glucantime
  • 7. Serious systemic illnesses (as judged by the physician)
  • 8. Participation in any drug trials in the last 60 days

研究者

发起方
World Health Organisation - Eastern Mediterranean Regional Office (EMRO) (Egypt)

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