CTRI/2023/09/057260尚未招募2 期
A clinical study to evaluate the efficacy of Lightinderm device augmented spot corrector serum use in reducing the hyperpigmented spots in healthy female subjects - NI
ightinderm0 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
- •1.Female adult subjects in general good health as determined from a recent medical history, general physical examination, dermatological assessment.
- •2.Subjects in the age group of 18-50 years (both ages inclusive).
- •3.Subjects with various skin types, including normal, dry, oily, and combination, while excluding those with sensitive skin.
- •4.Subjects with skin phototype III to VI
- •5.Subjects presenting with uneven skin tone and hyperpigmented spots on the face with a subset of 10 subjects with melasma
- •6.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.
- •7.Subject who agrees not to use any other product/treatment/home remedy/ except the provided product on their face during the study period other than the test and additional products of the study.
- •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, photography release and agree to come for regular follow-up.
- •11.Subjects willing to abide by and comply with the study protocol.
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 VISIA CR 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.Subjects who are pregnant and lactating
- •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.Subjects who have participated in any other clinical trial in the last 3 months.
- •13.Subjects who have undergone treatment with Botox/filler /bio stimulatory molecules injection in the past six months.
研究者
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