NCT03494140已完成不适用
Viscontour® Serum Med in Hydration of Facial Skin
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- Change of Subjective Therapy Evaluation (Questionnaire) compared to Baseline
研究概览
简要总结
The objective of this study is to confirm the clinical safety and efficacy of Viscontour® Serum Med in the hydration of facial tissue.
研究设计
- 研究类型
- Observational
- 观察模型
- Other
- 时间视角
- Prospective
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- Female
- 接受健康志愿者
- 否
入选标准
- •Females ≥ 18 years of age and in good general health condition
- •Signed informed consent
- •Existing Viscontour® Serum Med recommendation (i.a. for hydration, soothing, nourishing and refreshing the complexion and for use in combination with a day cream)
排除标准
- •Known hypersensitivity to one of the Viscontour® Serum Med components
- •Known pregnancy or lactating females
- •Subjects not capable of contracting and of understanding the nature, risks, significance and implications of the clinical investigation and unable to form a rational intention in the light of these facts
- •Subjects unable to understand informed consent or having a high probability of non compliance to the study procedures and / or non completion of the study according to investigator's judgement (e.g. illiteracy, insufficient knowledge of local language)
结局指标
主要结局
Change of Subjective Therapy Evaluation (Questionnaire) compared to Baseline
时间窗: 20 Minutes, Day 7 and Day 28
Change of Skin Parameters compared to Baseline
时间窗: 20 Minutes, Day 7 and Day 28
Routine Evaluation of the Overall Skin Condition
Incidence of Treatment-Emergent Adverse Events
时间窗: Up to Day 28
次要结局
未报告次要终点
研究者
研究点 (1)
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