jRCT2031240672尚未招募不适用
A double-blind comparative study of BFE1224 in patients with tinea pedis.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 入组人数
- 120
- 主要终点
- -
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized Controlled Trial
- 干预模型
- Parallel Assignment
- 主要目的
- Treatment Purpose
- 盲法
- Double Blind
入排标准
- 年龄范围
- 18age old over 至 No limit（—）
- 性别
- All
入选标准
- •Patients with tinea pedis in both feet or either foot.
- •Patients who have been confirmed to have dermatophyte elements by direct microscopic examination.
- •Patients in whom dermatophytes (Trichophyton species) have been identified by fungal culture.
- •Japanese patients aged 18 years or older at the time of consent.
排除标准
- •Patients with clinically significant hepatic dysfunction.
- •Patients with diseases or symptoms other than tinea pedis in the foot to be evaluated.
- •Patients who have used oral antifungal agents within 12 weeks prior to obtaining consent, or who are currently using them.
- •Patients who have used topical antifungal agents or topical treatments for onychomycosis on the foot to be evaluated within 4 weeks prior to obtaining consent, or who are currently using them.
结局指标
主要结局
-
Cure rate at 12 weeks after the start of treatment.
次要结局
未报告次要终点
研究者
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