CTRI/2018/02/012199已完成未知
To evaluate the in-vivo safety & efficacy of Skin care formulation on healthy female subjects of varied eye conditions (Normal Condition, Sensitive Condition & Contact Lens Users) and varied skin conditions (Normal, Oily, Dry & Combination) in terms of makeup removal formulation. - not applicable
ITC LIMITED ITC Life Sciences and Technology Centre0 个研究点目标入组 39 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 39
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Observational
入排标准
入选标准
- •Skin is healthy (free of eczema, wounds, inflammatory scarâ?¦.)
- •Healthy subjects (no infectious and evolutive pathology which could make the subject vulnerable and stop the study, no pathology which could interfere with the study, no symptom in the process of an exploratory checkup)
- •female volunteers in the age group of 18 to 40 .
- •Subjects representing varied skin types (ideally equal representation of all 4 skin types â?? Oily, Normal, Dry and combination)
- •Subjects representing varied eye conditions (ideally equal representation of Normal Condition, Sensitive Condition, and Contact Lens Users).
- •Volunteer Habitual of applying makeup.
- •Volunteer Habitual waterproof make up.
排除标准
- •Being pregnant or breastfeeding or having stopped to breastfeed in the past three months
- •Having refused to give her assent by not signing the consent form
- •Volunteer Taking part in another study liable to interfere with this study
- •Volunteer Being insulin-dependent diabetic or non insulin-dependent diabetic with a recent therapy (less than 6 months)
- •Volunteer Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products or food products or to latex
- •Having a progressive asthma (either under treatment or last fit in the last 2 years)
- •Volunteer Being epileptic
- •Volunteer Having non stabilized thyroid problems (requirement of a stabilized treatment for at least 6 months)
- •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).
- •Volunteer Having cutaneous hypersensitivity.
- •Volunteer Having a diagnosed or highly probable allergy to one or several compounds of the cosmetic products.
- •Volunteer Having undergone a surgery requiring a general anaesthetic of more than one hour in the past 6 months.
- •Volunteer Having changed her cosmetic habits in the 14 days preceding the start of the study on the studied anatomic unit.
- •Having applied a cosmetic product (included make-up) on the studied areas the first day of the study
- •Volunteer Having ocular problems (stye, chalazion, conjunctivitis).
- •Volunteer Having known history or present condition of allergic response to any cosmetic products (eye/ facial cosmetic products).
- •Volunteer Having eye infection or allergy.
- •Volunteer Having extremely sensitive eye condition.
- •Volunteer Having any form cutaneous disease which may influence the study result.
研究者
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