A Randomised Controlled study to assess the effectiveness of Bruhtyadi Choorna Yonidhoopan in comparison with Candid ointment in Yonikandu in Kaphaj Yonivyapad w.s.r. Vulvovaginal Candidiasis.
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 68
- 试验地点
- 1
- 主要终点
- To study the effectiveness of Bruhtyadi Choorna Yonidhoopan in Yonikandu in Kaphaj Yonivyapad.
研究概览
简要总结
The current study aimed as Evaluation of effect of Bruhtyadi Churna Yonidhoopan in comparison with candid Ointment in Yonikandu in Kaphaj Yonivyapad an Randomised Control study. Total 68 diagnosed patients of Yonikandu are equally divided into two groups, namely experimental and control group. The symptoms are yonikandu, yonipaichilya,yonishitalata etc. Yonidhoopan of bruhtyadi churna used as experimental group will be given for 10days. Candid ointment used as control group will be given for 10 days. Assessment for both will be done at 0th, 7th, 14th, days.Assessment done on the basis of subjective criteria.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 盲法
- None
入排标准
- 年龄范围
- 25.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •Patients under reproductive age group of 25-35 years.
- •Patients complaining of Yonikandu (Vaginal Itching).
- •Womens who are sexually active.
- •Patients with complaints of yonikandu for less than 15 days.
排除标准
- •Patients in menstrual bleeding phase.
- •Patient with Chronic PID.
- •Patient with genital malignancy.
- •Under prolonged use of antibiotics.
结局指标
主要结局
To study the effectiveness of Bruhtyadi Choorna Yonidhoopan in Yonikandu in Kaphaj Yonivyapad.
时间窗: The study will be conducted for 10 days follow up on day 1,day 7, day 14.
次要结局
- 1.Establish the best possible comparison of yonikandu with vulvovaginal candidiasis.(2.For Validation of treatment given in ayurvedic granthas.)
研究者
Dr Bhagyashri Satish Salunkhe
Dr. G.D.Pol Foundation, YMT Ayurvedic Medical College, Kharghar