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临床试验/CTRI/2018/05/013875
CTRI/2018/05/013875已完成不适用

A Comparative Clinical Study of Palashapushpa and Plaksha twak On its Sangrahi Karma w. s. r. to Shwetapradara

Government Ayurved Hospital Vadodara1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2018年4月6日最近更新:

试验速览

阶段
不适用
状态
已完成
发起方
入组人数
30
试验地点
1
主要终点
Change in the clinical symptoms of leucorrhoea

研究概览

简要总结

The Study is a Randomized clinical trial to evaluate the Sangrahi karma of Palasha pushpa churna and Plaksha twak churna on Shwetapradara (leucorrhoea). Total 30 patients will be enrolled in present study. Selected patients will be divided in 2 group on the basis of computer generated randomization. In this study Palasha pushpa churna will be given in dose of 3 gm two times before food with honey for 4 weeks and Plaksha twak churna will be given in dose of 3 gm two times before food with honey for 4 weeks. Folllow up will be **2 weeks.**The clinical data obtained will be summarized at the end of the study. Conclusion will be made after the statistical analysis of the data. 

Stastically Palashapushpa churna has significantaly result than Plaksha twak churna.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Open Label

入排标准

年龄范围
18.00 Year(s) 至 50.00 Year(s)(—)
性别
Female

入选标准

  • Age between 18 to 50 years of female patients.
  • Patient having complaints of Yonigata Shwetasrava.
  • Patients will be selected without consideration of bar of race and religion.

排除标准

  • Per vaginal white discharge due to other pathological conditions like- •Cervical or uterine malignancy • Pathological conditions like cervicitis, vaginitis, cervical erosion, PID.
  • Pregnant patient.
  • Uncontrolled systemic Diseases like HTN, DM.

结局指标

主要结局

Change in the clinical symptoms of leucorrhoea

时间窗: 4 weeks

次要结局

  • Safety(4 weeks)

研究者

发起方
Government Ayurved Hospital Vadodara
申办方类型
Research institution and hospital

研究点 (1)

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