A clinical study to evaluate the Anti-dandruff efficacy of ayurvedic products - NI

Hindustan Unilever Limited0 个研究点目标入组 0 人开始时间: 待定最近更新: 2023年10月16日

试验速览

暂无简介。

•1. Volunteer presenting moderate to severe dandruff (at least shoulder length hair for females) as per dermatological assessment.
•2. Volunteer in good health condition as per the medical screening criteria with no disease state or physical condition that the Investigator believes could interfere with the interpretation of the data.
•3. Volunteer able to read, understand and sign an appropriate informed consent form indicating her willingness to participate.
•4. Volunteers agreeing to comply with following study restrictions:
•-Volunteers Willing to refrain from application of any other product/treatment on their scalp and hair shafts during the study period.
•-Not to apply any cosmetic, hair care product, test product and/or water 48 hours before scheduled visits.
•-Willing not to colour or dye their hair just before the study visits and during the study period

•1. Volunteer pregnant or planning to become pregnant.
•2. Volunteers who are breastfeeding or having stopped to breastfeed in the past three months.
•3. Volunteers with any other signs of significant local irritation, erythema or skin disease on scalp as well as on the visible parts of the body skin site.
•4. Volunteers with self-perceived sensitive skin.
•5. Volunteers having chronic illness or had major surgery in the last year.
•6. Volunteers undergoing any treatment of any skin condition on body.
•7. Volunteers taking medication continuously/regularly every day such as corticosteroids or non-steroidal anti-inflammatories, topically for four weeks or orally for eight weeks prior to the study.
•8. Volunteers taking medication for any condition which the Investigator believes may influence the interpretation of the data.
•9. Volunteers on food supplements

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