TCTR20220214004已完成1 期
Human Repeated Insult Patch Test[HRIPT] of Blackmores Natural Vitamin E Cream product
Blackmore Limited0 个研究点目标入组 109 人开始时间: 2022年2月14日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 109
研究概览
简要总结
All of the test products (Natural Vitamin E Cream Lanolin, Natural Vitamin E Cream Firm & Smooth Skin, Natural Vitamin E Cream PABA Free and Natural Vitamin E Cream Skin Barrier were not irritants or sensitizers (No reaction was observed at any time)
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20 Years 至 60 Years（—）
- 性别
- All
入选标准
- •1. Male and female age between 20-60 years, in general good health based on study screener [no physical required]
- •2. Individuals who have normal to sensitive skin classified by self-perceived using a Participant screening form and Sensitive Questionaire
- •3. Individuals who have normal any skin type or ethnicity, provided their degree o skin pigmentation does not significantly interfere with evaluations. Skin type I to IV according to Fitzpatrick scale is preferred
- •4. Individuals who are free from any dermatological disordor such as wound, psoriasis, rosacca, atopic dermatitis including a know history of allergies
排除标准
- •1. Woman who are pregnant, nursing or planning on becomimg pregnant during the course of the study
- •2. Individuals with any visible dermatological condition [e.g. psoriasis] the could interfere with evaluations
- •3. Individuals with abnormal skin pigmentation at the test sites that could interfere with subsequent evaluations of dermal responsiveness or individuals who have skin type of V or VI based on Fitzpatrick scale
- •4.Individuals who take medications that could interfere with the test results, including any regimen of steroidal/non-steroidal anti-inflammatory drugs or antihistamines
- •5. Individuals who are allergic to cosmetics or personal care products
- •6. Individuals who are currently under treatment for asthma or diabetes
- •7. Individuals who currently enroll in clinical study or participation in a patch test study within 14 days prior to the start of this study
研究者
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