TCTR20161008001招募中未知
Comparison of efficacy and safety of 0.01% Bimatoprost and 0.1%Tacrolimus in the treatment of facial vitiligo
Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital0 个研究点目标入组 40 人开始时间: 2016年10月8日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 招募中
- 发起方
- 入组人数
- 40
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
- 15 Years 至 90 Years（—）
- 性别
- All
入选标准
- •- facial vitiligo patient
- •- other affected vitiligo area less than 2% BSA
排除标准
- •- apply topical steroid within 7 days
- •- on current medication effected skin pigmentation within 2 weeks
- •- on current treatment of vitiligo such as oral medication, NBVUB, PUVA, systemic steriod within 1 month
- •- allergy to bimatoprost and protopic
- •- pregnancy and breast feeding patient
- •- underlying disease: asthma
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