TCTR20160912002已完成3 期
A pilot study comparing efficacy and safety of topical 3% minoxidil solution with topical 3% minoxidil solution combined with topical 0.25% finasteride solution in treatment of female pattern hair loss.
Division of Dermatology, Ramathibodi Hospital, Mahidol University0 个研究点目标入组 30 人开始时间: 2016年9月12日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 已完成
- 发起方
- 入组人数
- 30
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
- 18 Years 至 0 Years（—）
- 性别
- Female
入选标准
- •1.Healthy female subject
- •2.Diagnosis of female pattern hair loss
- •3.Agree to participate and signed informed consent form
排除标准
- •1.History of hair transplant
- •2.Applying topical hair growth products within 2 weeks
- •3.Receiving light and laser treatment of the scalp within 3 months
- •4.Taking oral finasteride within 12 months
- •5.Taking dutasteride within 18 months
- •6.History of systemic illness
- •7.History of scalp diseases eg. seborrheic dermatitis, scalp infection.
- •8.Pregnancy or breast feeding
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