TCTR20171130004已完成3 期
Comparison of the efficacy and safety using 0.01% vs 0.03% bimatoprost for the treatment of eyebrow hypotrichosis: A randomized, double-blind study
Division of Dermatology, Department of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol0 个研究点目标入组 30 人开始时间: 2017年11月30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 N/A (No limit)（—）
- 性别
- All
入选标准
- •1.Patients with eyebrow hypotrichosis
- •2.Age more than 18 year-old
- •3.No serious underlying diseases
- •4.Informed consent
- •5.Compatible with follow-up schedule
排除标准
- •1.Patients undergone eyebrow transplantation
- •2.Previously treated with drugs or products affecting eyebrow cycle within 2 wks
- •3.Previously treated with minoxidil, systemic antiandrogen, topical estrogen/progesterone, topical prostaglandin analogs, anabolic steroids, lithium, phenothiazines
- •4.Patients with underlying diseases involving eyebrow hypotrichosis eg. Cancer, immunocompromised, thyroid diseases or psychiatric disorders including trichotillomania
- •5.Patients undergone eyebrow tattooing
- •6.Patients with history of poor wound healing or with skin pathology on eyebrow
- •7.Allergic to bimatoprost
- •8.Pregnancy or lactation
- •9.Withdraw
研究者
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