TCTR20201227001Enrolling By Invitation2 期
Efficacy and safety of a hair growth promoting product containing topical 1% melatonin for treatment of androgenetic alopecia in women: A randomized double-blind trial
Faculty of Medicine, Thammasat University (Rungsit campus)0 个研究点目标入组 100 人开始时间: 2020年12月27日最近更新:
适应症
试验速览
- 阶段
- 2 期
- 状态
- Enrolling By Invitation
- 发起方
- 入组人数
- 100
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 65 Years（—）
- 性别
- Female
入选标准
- •1. Female pattern hair loss (Androgenetic alopecia), Type II - V of Sinclair scale
- •2. Healthy status
排除标准
- •1. No topical treatment include minoxidil for AGA within 6 months
- •2. No topical herb solution for hair growth within 6 months
- •3. No systemic treatment for AGA within 6 months. For example, oral contraceptive drug, finasteride, dutasteride, spironolactone
- •4. No history of chemotherapy and radiation within 1 year prior to the clinical trials
- •5. No topical steroid that apply a scalp at least 14 days within 3 months prior to the trials
- •6. No pregnancy and breastfeeding status
- •7. No history of hypersensitivity to melatonin and minoxidil
- •8. No multiple comorbidities
研究者
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