Comparative Clinical Study of Arjuna Twaka Kashaya Yonidhawana and Kankshi Siddha Jal Yonidhawana in Shwetpradara w.r.s. to Cervical Erosion.
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 80
- 试验地点
- 1
- 主要终点
- -Low back pain
研究概览
简要总结
Primary Objective
To Compare the efficacy of Arjuna Twaka Kashaya Yonidhawana in Shwetapradara.
To Compare the efficacy of Kankshi Siddha Jal Yonidhawana in Shwetapradara.
Secondary Objective
To carry out the study of Shwetpradara w.s.r.to Cervical Erosion in detail by Ayurvedic and modern perspective.
To observe and compare the obtained data.
To study the concept of Yonidhawana in view of Ayurved literature and to raise the awareness of Yonidhawana process.
Patients will be divided into two groups.
GROUP A
GROUP B
Clinical assessment on 0th, 3rd,5th,7th Day
Duration of drug administration 7 Days
Follow up:
After bleeding phase of 0,3rd,5th, and 7th day
inclusion Criteria :
AGE - 20-40 years, Married Women
Vaginal discharge Itchinglow backachecervical ectropion
Exclusion Criteria:
Unmarried women
Pregnant women
Patients having Cervical polyp
Patients having Cervical malignancy
Patient who are serological positive i.e., HIV, VDRL.
Withdrawal Criteria: The patient who wishes to discontinue and not ready for further participation in study will be discontinued.
During the study, if any complication occurs, these patients will be excluded from the study, and she will be given management accordingly.
The patient who did not continued follow up for two consecutive visits will be treated as discontinued.
Primary outcome -reduce signs and symptoms of Shwetapradar.
Secondary outcomes -no reccurance of Shwetapradar
All data will be collecting from clinical case studies will be presented in the form of graphs, charts, healing grade etc.
Patients will be observed before and after treatment. All observed data collected after the final assessment will be subjected to statistical analysis
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 盲法
- None
入排标准
- 年龄范围
- 20.00 Year(s) 至 40.00 Year(s)(—)
- 性别
- Female
入选标准
- •Married women.
排除标准
- •Unmarried Women -pregnant women -Patients having Cervical polyp -Patients having Cervical malignancy -Patient who are serological positive ie HIV,VDRL.
结局指标
主要结局
-Low back pain
时间窗: 7 days
Signs cervical ectropion cervical erosion
时间窗: 7 days
To Reduce symptoms -Vaginal discharge itching at vaginal region
时间窗: 7 days
次要结局
- TO Reduce the recurrence of Shweta pradnya(30 days)
研究者
Dr Poonam Shahajirao Nagtilak
Shree Saptashrungi ayurved Mahavidyalaya
