CTRI/2023/03/050575已完成Unknown
A clinical study to evaluate Safety, In-Use Tolerability and Efficacy of HTSS-052203 in reducing the facial dark spots in Healthy Adult Subjects.
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 入组人数
- 42
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) Subject has at least 2 dark spots on the face (suntan, blemishes, sunspots and age-spots). Preferably equal number of subjects will be recruited in all indications.
- •2) Subjects with mild to moderate dark spots as per Investigator global assessment (IGA).
- •3) Subjects with oily skin having Sebumeter measurement > 180 (μg/cm2).
排除标准
- •1) Subjects having any active dermatological skin diseases (e.g., psoriasis, atopic dermatitis, rosacea etc.), that might interfere with clinical assessments.
- •2) Subjects who are receiving topical or systemic treatments / undergoing skin lightening treatment.
- •3) Subjects receiving medications (e.g., steroids or antihistamines) which would compromise the study.
- •4) Subjects with chronic illness which may influence the cutaneous state.
- •5) Subjects having history of diabetes, acute cardiac and circulatory diseases, HIV, hepatitis.
- •6) Subjects using other marketed anti-acne/anti-aging/skin lightening products during the study period or in the past 6 weeks.
研究者
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