NCT00497783已完成4 期
Safety Dermatological Evaluation of the Acceptability With Gynecological Follow up for Dermacyd Femina Delicata
适应症
相关药物
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- Sanofi
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Clinical and local tolerability
研究概览
简要总结
The purpose of this study is to demonstrate the safety of the gynecological formulation in normal and usual usage condition of Dermacyd Femina Delicata.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Supportive Care
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 60 Years（Adult）
- 性别
- Female
- 接受健康志愿者
- 是
入选标准
- •Integral skin in the tested region
排除标准
- •Pregnancy or breastfeeding women
- •Use of Anti-inflammatory or immune-suppression drugs
- •Topical medication use at the tested region
- •Active cutaneous gynaecological disease which may interfere in study results
- •Personal history of allergic disease at the area to be treated
- •Allergic or atopic history
- •The above information is not intended to contain considerations relevant to a patient's potential participation in a clinical trial.
结局指标
主要结局
Clinical and local tolerability
时间窗: 21 days
Adverse events and their association with the treatment.
时间窗: 21 days
次要结局
未报告次要终点
研究者
研究点 (1)
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