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临床试验/IRCT20211211053349N1
IRCT20211211053349N1已完成3 期

Evaluation of the effectiveness of topical gel treatment containing standardized 5% hydroalcoholic extract of Zataria multiflora in comparison with intra lesional(IL) glucantime in the treatment of cutaneous leishmaniasis in human

Kerman University of Medical Sciences0 个研究点目标入组 80 人开始时间: 待定最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
入组人数
80

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
5 years 至 no limit(—)
性别
All

入选标准

  • Patients must be 5 years old or older.
  • The patient can be of both sexes.
  • The number of wounds should not be more than 5.
  • No sores on the face or ears.
  • Affirmation of parasitic infection is required
  • The patient has cutaneous leishmaniasis.
  • The onset of their disease is less than 4 months

排除标准

  • Pregnant women are excluded from the study.
  • Patients with severe hypoglycemia are excluded from the study.
  • Breastfeeding women are excluded from the study.
  • Patients who have been treated with other methods (systemic Glucantime, combination therapy, etc.)
  • patients who have been treated in other clinical trial

研究者

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