EUCTR2008-006756-22-BE进行中（未招募）不适用
VVS study: the efficacy and safety of Bio-restorative Skin Cream in the local treatment of vulvar vestibulitis syndrome (VVS) compared with placebo. - VVS study
eocutis0 个研究点目标入组 30 人开始时间: 2009年1月9日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 发起方
- 入组人数
- 30
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- Female
入选标准
- •age between 18 and 50
- •minimum 6 months suffering of VVS
- •Visible redness of the vestibule (5 and 7 and/or 1 and 11 o clock)
- •good general health
- •not pregnant or becoming pregnant during the study.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years)
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Use of corticoids, anti-inflammatory or immunosuppressive medication during the last two weeks before study entry.
- •Previous extensive vestibular surgery.
- •Suffering chronic diseases that need long term treatment.
- •Use of spermacides as a contraception
- •needing suplemental treatment for acute vulvovaginitis.
- •No use of other vestibulitis medications and treatments
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