ISRCTN33310512已完成未知
Efficacy and tolerability of a topical skin-lightening CPP on subjects presenting facial dyspigmentation compared with 4% hydroquinone
ISISPHARMA0 个研究点目标入组 43 人开始时间: 2019年1月30日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 43
研究概览
简要总结
2019 results in https://www.ncbi.nlm.nih.gov/pubmed/31858658 (added 19/02/2020)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Women or men
- •2. Aged between 18 and 60 years
- •3. Skin phototype IV-V
- •4. Presenting facial dyspigmentation due to melasma as determined by Wood’s light examination
排除标准
- •1. Pregnant or nursing women or women planning to get pregnant during the study
- •2. Subjects with a cutaneous pathology on the study zone (eczema)
- •3. Subjects having undergone surgery under general anaesthesia within the previous month
- •4. Individuals who have been excessively exposed to sunlight or UV-rays within the previous month
- •5. Subjects having used topical or systemic treatment during the previous weeks liable to interfere with the assessment of the cutaneous acceptability of the study product
研究者
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