CTRI/2018/04/013504已完成未知
An exploratory study to investigate cleanser formulations for their efficacy on Skinimperfections (acne and skin respect) through instrumental and dermatologist assessment,over a 4 week daily home usage
Oreal India Pvt Ltd0 个研究点目标入组 152 人开始时间: 待定最近更新:
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 152
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. Healthy female Indian volunteers, aged 18 â?? 45 years (both inclusive)
- •2. Subjects with casual sebum levels >= 80 μg/cm2 and Sebum Excretion Rate >= 50 μg/cm2
- •3. Subjects having atleast 5 inflammatory and no more than 15 inflammatory lesions over
- •the whole face, out of which atleast 2 are papules of size > 0.5 mm and evolved in last
- •5 days (basis the medical history)
- •4. Subjects having at least 10 non-inflammatory acne lesions and not more than 50 non-inflammatory acne lesions over the whole face, out of which at least 50% are open comedones (black heads)
- •5. Subjects with medium to dark skin color having ITA values between >= 10 and <= 41
- •6. Subjects having at least two Post Inflammatory Hyper pigmentation spots of size 3 mm or more
- •7. Subjects with adequate representation of normal and sensitive skin
- •8. Females with a stable hormonal status, as self-declared by subjects
- •9. Subject who agrees not to use any other product/treatment/soap bar/any other cleanser
- •on their face during the study period
- •10. Subject who agrees not to carry out bleaching or any other procedures including facial etc. on face during the study period
- •11. Subject who agrees to remove all jewellery on/around face (e.g., necklace, earrings,
- •nose ring), during VISIA imaging
- •12. Female subject with child-bearing potential willing to undergo Urine Pregnancy Test
- •and to use acceptable methods of contraception
- •13. Subjects who are able to give written informed consent and to comply with the
- •requirements of the study
- •14. Subjects who are ready to follow instructions and study restrictions during the study period
排除标准
- •1. Known hypersensitivity to any of the study products or constituents
- •2. Any significant skin pathology in the test area, like rosacea, severe acne, or eczema
- •3. Subjects on any topical or systemic treatment that could interfere with the study
- •treatments/assessments (topical benzoyl peroxide and other anti-acne or anti-seborreic
- •products, antibiotics, corticosteroids, retinoids, anti-inflammatory drugsâ?¦) within the
- •last 4 weeks prior to participation in the study, and during the study
- •4. Subjects who are having chronic illness or had major surgery in the last year
- •5. Subject with any significant medical condition that would interfere with the
- •participation in the trial
- •6. Subject who are allergic or sensitive to bar cleansing products/face cleansers/
- •creams/lotions, artificial jewellery or anything else
- •7. Females in pregnancy or lactation at the beginning of the study or planned during the
- •8. Subject reported or planning to sun-bathe or to overexpose to UV-light (mountain, sports, phototherapy, tanning salon useâ?¦) for aesthetic or therapeutic reasons the month before the study start or during the study
- •9. Participation in any other clinical trial up to 1 month prior to screening and during the
- •10. Any topical or systemic treatment(s) such as NSAIDs, corticosteroids, retinoids,
- •vitamins , etc. that, in the investigatorâ??s judgement, could interfere with the study
- •treatments / assessments, taken 2 weeks prior to inclusion and / or planned during the
- •11. Subjects Who have started, stopped or changed their hormonal treatment(s) (including
- •contraceptive pill) in the previous one month prior to the study
研究者
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