CTRI/2023/10/059282已完成Unknown
A double-blind, randomized, single centre, two-arm, placebo-controlled, comparative clinical study to evaluate the safety, in-use tolerability and efficacy of Moisturizing Cream in female subjects with varied skin type. - NI
DPKA Universal Consumer Ventures Private Limited0 个研究点目标入组 96 人开始时间: 待定最近更新:
试验速览
- 阶段
- Unknown
- 状态
- 已完成
- 发起方
- 入组人数
- 96
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) Subjects with dry / normal / oily / sensitive skin.
- •oSubjects with self-perceived normal skin.
- •oSubjects with dry (readings between 30 – 40) as assessed by MoistureMeterSC.
- •oSubjects with oily skin having Sebumeter measurement > 150 (µg/cm2).
- •oSubjects with sensitive skin based on Dr. Baumann’s skin type questionnaire.
- •2) Subjects having good general health as determined by the Investigator on the basis of medical history.
- •3) Females of Childbearing potential must have a negative urine pregnancy test performed during Visit 01.
排除标准
- •1) Subjects undergoing treatment for skin lightening or subjects using other marketed skin lightening products during the study period or in the past 6 weeks.
- •2) Subjects who are receiving topical or systemic treatments.
- •3) Subjects receiving medications (e.g., steroids or antihistamines) would compromise the study.
- •4) Chronic illness which may influence the cutaneous state.
- •5) Subjects having any active dermatological skin diseases (e.g., psoriasis, atopic dermatitis, rosacea etc.), that might interfere with clinical assessments.
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