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临床试验/CTRI/2025/01/079311
CTRI/2025/01/079311尚未招募2 期

Comparative Clinical Study of Arjuna Twaka Kashaya Yonidhawana and Kankshi Siddha Jal Yonidhawana in Shwetpradara w.r.s. to Cervical Erosion.

Shree Saptashrungi ayurved Mahavidyalaya and hospital Nashik1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2025年2月2日最近更新:

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

发起方
Shree Saptashrungi ayurved Mahavidyalaya and hospital Nashik
申办方类型
Private medical college
责任方
Principal Investigator
主要研究者

Dr Poonam Shahajirao Nagtilak

Shree Saptashrungi ayurved Mahavidyalaya

研究点 (1)

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