TCTR20171104001尚未招募3 期
A randomized, controlled, split-face clinical trial comparing combination of ProACNE SOLUTION ACTIVE CLEAR with 2.5% benzoyl peroxide versus 2.5% benzoyl peroxide with placebo in the treatment of mild to moderate degree of acne vulgaris
Beiersdorf (Thailand) Co., Ltd0 个研究点目标入组 19 人开始时间: 2017年11月4日最近更新:
适应症
试验速览
- 阶段
- 3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 19
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 40 Years（—）
- 性别
- All
入选标准
- •- age 18 - 40 years old
- •- mild to moderate degree of acne vulgaris, according to Leeds revised acne grading
排除标准
- •- pregnant or breast-feeding woman
- •- allergic to benzoyl peroxide or any ingredient of ProACNE SOLUTION ACTIVE CLEAR (salicylic acid, L-carnitine, decylene glycol, licochalcone A)
- •- deny to discontinue topical therapy of acne more than 14 days before starting treatment.
- •- denial to discontinue topical therapy of acne more than 14 days before starting treatment.
- •- denial to discontinue systemic therapy of acne more than 28 days before starting treatment.
- •- irregular menstruation or known case of PCOS
研究者
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