CTRI/2020/06/025644尚未招募2 期
Clinical validation of natural plant based skincare supplement in healthy subjects
Climic Health Pvt Ltd0 个研究点目标入组 0 人开始时间: 待定最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
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
- •Male/ Female of 18 to 40 years, willing to give a written informed consent and come for regular observations
- •Subject is a healthy adult, female, in the age range of 18 and 40 years
- •Subject with dull complexion, dry/oily skin with/ without uneven texture and with at least 2 hyperpigmentary spots as a result of photodamage.
- •Mild acne without nodular abscesses
- •Subject has not participated in a similar clinical investigation in the past three months.
- •Subject who is willing to abstain from using any fairness product, sunscreens, natural/ Ayurvedic treatments or other home remedies and also willing to abstain from undergoing any facial treatments such as facial masks, packs, bleaching, etc either at home or at beauty parlour during the entire study course. In case of having used fairness product in the near past, should be willing to undergo a wash out period of 1 week, wherein they should abstain from applying any product other than the suggested cleanser on face.
- •Female subjects of reproductive age group should undergo
排除标准
- •Subject with a known history or present condition of allergic response to any cosmetic/pharmaceutical products, toiletries or their ingredients including fragrance.
- •Subject who has used any systemic medication (antibiotics, retinoid, steroids, spironolactone or any anti acne medication) within past 4 weeks or any topical facial medication within 2 weeks prior to study commencement, which could compromise the study.
- •Subject with a medical history of disease or condition or a concurrent illness or pre- existing or dormant dermatologic condition (psoriasis, rosacea, rashes, eczema etc.) that could interfere with the study results.
- •Subject with excessive facial hair or scars, which could interfere with evaluation. Subject with a history of having used a similar product during or since 1 week prior to the scheduled study commencement.
- •Subject who is currently pregnant (as confirmed by the urine pregnancy test) or nursing or contemplating pregnancy during the study course.
- •Subject who has used any systemic medication (antibiotics, oral contraceptive pills, retinoid, steroids, spironolactone or any anti acne medication) within past 4 weeks or any topical facial medication within 2 weeks prior to study commencement, which could compromise the study.
- •Subject with a medical history of disease or condition or a concurrent illness or pre- existing or dormant dermatologic condition (psoriasis, rosacea, rashes, eczema etc.) that could interfere with the study results.
- •Patient with known history of acute / chronic liver or kidney disease.
研究者
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