CTRI/2017/12/010947招募中2 期
An open clinical trial to evaluate the effect of Yonipichu with Dhanvantara taila in Paripluta Yonivyapat wsr to Dyspareunia
drnamratabbhagaje1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2017年2月15日最近更新:
试验速览
- 阶段
- 2 期
- 状态
- 招募中
- 发起方
- 入组人数
- 10
- 试验地点
- 1
- 主要终点
- 1.Reduction in pain during intercourse according to VAS scale
研究概览
简要总结
Above study is an open clinical single group study in patients with mentioned complaints in between age group of 20-45yrs, who will undergo treatment of yonipichu with dhanvantara taila 30ML for 7 days with follow up after 15days of treatment .
At the end of the treatment after 15days
1.Pain
-
Dry vagina
-
Frequency of intercourse will be assessed
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 20.00 Year(s) 至 40.00 Year(s)(—)
- 性别
- Female
入选标准
- •1.Pain during the intercourse 2.Dry vagina 3.Failure of orgasm 4.Married female patients of sexually active group 20- 45yrs.
排除标准
- •1.Tough imperforate hymen 2.Narrow introitus 3.Pregnancy 4.Known cases of Benign and malignant condition of cervix 5.Known cases of Veneral diseases.
结局指标
主要结局
1.Reduction in pain during intercourse according to VAS scale
时间窗: 1.Reduction in pain during intercourse according to VAS scale | 2.Increase in number of sexual intercourse weekly
2.Increase in number of sexual intercourse weekly
时间窗: 1.Reduction in pain during intercourse according to VAS scale | 2.Increase in number of sexual intercourse weekly
次要结局
未报告次要终点
研究者
研究点 (1)
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