To evaluate the in vivo safety and efficacy of a skin care formulation in terms of reduction in tanning and improvement in the skin brightness on healthy Female subjects
试验速览
- 阶段
- 不适用
- 状态
- 尚未招募
- 发起方
- 入组人数
- 33
- 试验地点
- 1
- 主要终点
- Tan reduction and improvement in skin brightness
研究概览
简要总结
OBJECTIVE- The objective of this study will be to evaluate the in vivo safety and efficacy of a skin care formulation in terms of reduce tanning and to improve the skin brightness on healthy Female subjects coded:
The evaluation is performed using, Subject Self Evaluation, Dermatological Evaluation- Cosmetic Acceptability, Chromametry
POPULATION- 33 Subjects (30 completed cases) Female subjects will be selected for the study.
The subjects selected for this study are healthy female aged between 20 and 35 years, having Dull and Tanned skin.
STUDY DURATION- 30 minutes following the first application of the product.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- Participant and Outcome Assessor Blinded
入排标准
- 年龄范围
- 20.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •1.Indian female subjects 2.Healthy subjects 3.Skin is healthy on the studied anatomic unit 4.Having Dull and Tanned skin.
排除标准
- •Being pregnant or breastfeeding or having stopped to breastfeed in the past three months
- •Having refused to give her/his assent by not signing the consent form
- •Taking part in another study liable to interfere with this study
- •Being insulin-dependent diabetic or non-insulin-dependent diabetic with a recent therapy (less than 6 months)
- •Having a progressive asthma (either under treatment or last fit in the last 2 years)
- •Having a chronic dermatosis liable to modify the cutaneous reactivity on the tested area (except for specific studies on a determined dermatosis)
- •Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
- •Being epileptic.
- •Following a chronic medicinal treatment comprising any of the following products: aspirin-based products, anti-inflammatories, anti-histamines, corticotherapy, taken by general or local routes (the only medication permitted is paracetamol)
- •Having cutaneous hypersensitivity.
- •Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.
- •Having undergone a surgery requiring a general anesthetic of more than one hour in the past 6.
结局指标
主要结局
Tan reduction and improvement in skin brightness
时间窗: Baseline, 30 minutes after product removal.
次要结局
未报告次要终点
研究者
Dr Pooja Yadav
MASCOT-SPINCONTROL India Pvt. Ltd.