CTRI/2023/02/049513已完成未知
Clinical study to evaluate the efficacy of the Moisturizer in the improvement of skin moisturization in a full-face study design
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 36
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. Male and female subjects in general good health as determined from a recent
- •medical history, general physical examination, dermatological assessment.
- •2. Male and female subjects with early signs of aging
- •3. Subjects with presence of one or more spots or pigmentation/blemishes as per
- •Investigator discretion
- •4. Subjects in the age group of 35-50 years (both ages inclusive)
- •5. Subjects presenting dull and belonging to either one of the skin types dry,
- •normal or combination
- •6. Subjects who agree to refrain from using any creams, lotions, moisturizers,
- •sunscreens or any other skin products on the face for the duration of the study
- •other than the test product provided,
- •7. Subjects free of excessive hair, acne, cuts, abrasions, fissures, wounds,
- •lacerations, or any other active skin conditions on the face as determined by
- •the dermatologist.
- •8. Subjects who agree not to carry out bleaching or any other procedures including
- •facial etc. on face during the study period.
- •9. Subjects who agree not to expose to excessive sun light. (Sun exposure not
- •more than half an hour daily and during that time use of umbrella to cover face).
- •10. Subjects willing to give a voluntary written informed consent and photography
- •11. Subjects willing to abide by and comply with the study protocol,
- •12. Subjects who are willing not to participate in any other clinical study during
- •participation in the current study,
- •13. Subjects who have not participated in any clinical product evaluation test within
- •past 1 month,
- •14. Subjects able to read and sign an appropriate informed consent form indicating
- •his/her willingness to participate.
排除标准
- •1. Subject with any other signs of significant local irritation or skin disease.
- •2. Subject currently taking any medication, which the Investigator believes may influence the interpretation of the data.
- •3. Subject having clinically significant systemic or cutaneous disease, chronic illness or had major surgery in the last year.
- •4. Subjects who do not agree to remove all jewellery on/around face (e.g., necklace, earrings, if possible nose ring), during imaging.
- •5. Subjects having hair style which covers almost the entire forehead
- •6. Subjects undergoing any treatment of any skin condition on their face.
- •7. Subjects not willing to discontinue other topical facial products.
- •8. Subject allergic or sensitive to bar, cleansing products, cosmetics,
- •creams/lotions, artificial jewellery or anything else.
- •9. Pregnant women (as confirmed by UPT) and lactating women
- •10. Subjects on any medical treatment either systemic/topical in the past 1 month or currently taking medication including food supplements.
- •11. Subjects with skin allergy, history of atopic dermatitis or psoriasis
- •12. Any underlying uncontrolled medical illness including diabetes mellitus, hypertension, liver disease or history of alcoholism, HIV, hepatitis, or any other serious medical illness.
研究者
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