CTRI/2018/02/011928已完成未知
To evaluate the Safety & Efficacy of Facial Oxylife Spot Reduction Bleach System
试验速览
- 阶段
- 未知
- 状态
- 已完成
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
入选标准
- •1. Female Adult Subjects in general good health with age group of 18 to 60 years. Subjects who have not undergone any bleaching or facial procedure in past 6 weeks.
- •2. Subjects willing to give a voluntary written informed consent for the participation in study and also photography release and agree to come for regular follow up.
- •3. Subjects willing to abide by and comply with the study protocol.
- •4. Subjects who are willing not to participate in any other clinical study during participation in the current study.
- •5. Subjects who will qualify the sensitivity test will be enrolled in the study.
排除标准
- •1. A known history or present condition of allergic response/hypersensitivity to any cosmetic ingredients, or any ingredient of the test product.
- •2. Present/current of intense sun exposure.
- •3. Female volunteers with positive pregnancy test.
- •4. Presence of any underlying clinically significant uncontrollable medical conditions
- •5. Subject having active skin diseases (e.g. mild, moderate to severe acne vulgaris on the face or nodulocystic acne, psoriasis, active atopic dermatitis, lichen planus pigmentosus/Ashy dermatosis, pigmented contact dermatitis and active seborrhoeic dermatitis, tinea faciei or other cutaneous manifestations), which may interfere with the test readings.
- •6. Subject on systematic medications (e.g. steroids, anti-oxidant) which may compromise the study.
- •7. Subjects who have excessive facial hair
研究者
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