TCTR20181119004已完成未知
The safety evaluations of finished cosmetic products (PSF, PSDO, PSCN, CME) via Human Repeated Insult Patch Test (HRIPT)
nilever thai services co. ltd0 个研究点目标入组 33 人开始时间: 2018年11月19日最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 33
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
- 20 Years 至 60 Years（—）
- 性别
- Female
入选标准
- •-Female aged between 20-60 years, in general good health based on a study screener (no physical examination required)
- •- Individuals who have sensitive skin classified by self-self perceived using a Sensitive Skin Questionnaire
- •- Female volunteer of any skin type or ethnicity, provide their degree of skin pigmentation does not significantly interfere with evaluations
- •- Individual free of any systemic or dermatological disorder including a known history of allergies or other medical conditions which could interfere with the conduct of the study, interpretation of results or increase risk of adverse reactions
- •- Individuals who agree to refrain from swimming, using hot tubs/saunas and any type of tanning
- •- Individuals who are able to read, understand and provide written informed consent
- •- Individuals who agree to complete the course of the study and to comply with instructions
排除标准
- •- Women who are pregnant, nursing or planning on becoming pregnant during the course of the study
- •- Individuals with any visible dermatological condition (e.g. psoriasis) that could interfere with evaluations
- •- Individuals with abnormal skin pigmentation at the test sites that could interfere with subsequent evaluations of dermal responsiveness
- •- Individuals who take medications that could interfere with the test results, includind regimen of steroidal/ non- steroidal anti-inflammatory drugs or antihistamines
- •- Individuals who are allergic to cosmetics or personal care products
- •- Individuals who are currently under treatment for asthma or diabetes
- •- Individuals who are currently enroll in clinical study or participation in a patch test study with in 14 days prior to the start of this study
研究者
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