跳至主要内容
临床试验/CTRI/2018/07/015063
CTRI/2018/07/015063尚未招募不适用

Comparative study of efficacy of itraconazole and terbinafine with different doses and combination in the treatment of Tinea

IMS BHU1 个研究点 分布在 1 个国家目标入组 275 人开始时间: 2018年6月8日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
275
试验地点
1
主要终点
Complete clearance of skin lesions

研究概览

简要总结

this is a comparative study with two drugs (terbinafine and itraconazole) with recommended daily doses, double daily doses and combination of both drugs with daily doses. Total study period is of 8 weeks.

primary and secondary outcomes are complete clearing of skin lesions.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Not Applicable

入排标准

年龄范围
12.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Tinea cruris Tinea corporis Tinea faciei.

排除标准

  • weight more than 80 kg Any other co-morbidities like hepatic disorders, renal disorders, cardiac disorders, etc.
  • history of oral antifungal agents within one month of start of study.

结局指标

主要结局

Complete clearance of skin lesions

时间窗: every 2 weeks for 8 weeks

次要结局

  • Experienced as primary outcome.(Every 2 weeks for 8 weeks.)

研究者

发起方
IMS BHU
申办方类型
Government medical college

研究点 (1)

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