Assessment of the efficacy of a topical skin lightening product in healthy Indian female volunteers with dull skin and pigmented spots for 8 weeks - Not Applicable

Oreal India Pvt Ltd Research Innovation R I0 个研究点目标入组 65 人开始时间: 待定最近更新: 2021年11月24日

试验速览

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•Indian female subjects, aged 18-60 years (approximately 80% of total population is between 18 to 45 years age)
•All skin types (50% having sensitive skin) e.g. fair, wheatish, brown and dark brown with equal distribution of skin type across the group
•Subjects having pigmented spots and at least 1 well defined and homogenous spot <= 3mm with an adjacent spotless area, a dull skin tone
•on face and visible pores on cheek, presenting vascular homogeneity
•Subjects not applying any skin whitening product prior to 6 weeks of the start of the study
•Able to give written informed consent and to comply with the requirements of the study

•Any significant skin pathology in the test areas, like rosacea, severe acne, eczema & melasma
•Known hypersensitivity to the any of the study products or constituents
•Any topical or systemic treatment that could interfere with the study treatments/assessments (antibiotics, corticosteroids, retinoids, antiinflammatory drugsâ?¦) within the last 4 weeks prior to participation in the study, and during the study
•Any surgical treatment on the test areas (laser peel, dermabrasion, etc.)
•Subject reported or planning to sun-bath or to overexpose to UV-light (mountains sports, phototherapy, tanning salon use, etc.) for aesthetic or therapeutic reason the month before the study start or during the study
•Any significant medical condition that would interfere in the participation in the trial
•Participation in a clinical trial up to 1 month prior to inclusion
•Pregnant women (as confirmed by UPT) and lactating women

发起方

Oreal India Pvt Ltd Research Innovation R I