跳至主要内容
临床试验/CTRI/2025/06/089384
CTRI/2025/06/089384尚未招募3 期

A Randomised Controlled Clinical Trial To Study The Effect Of Palashadi Churna Orally And Guduchyadi Kwatha Yonidhawan In Kaphaj Yonivyapad With Special Reference To Trichomonas Vaginitis.

Dr Nupura Dilip Lakhan1 个研究点 分布在 1 个国家目标入组 70 人开始时间: 2025年7月7日最近更新:

试验速览

阶段
3 期
状态
尚未招募
发起方
入组人数
70
试验地点
1
主要终点
Reduction In Signs And Symptoms Of Kaphaj Yonivyapad After Taking Palashadi Churna Orally And Guduchyadi Kwath Yonidhwana.

研究概览

简要总结

Kaphaj yonivyapad is a common gynaecological problem and it hampers day to day activity of woman and make them go through mental trauma of fear and guilt.

The prevalence rate of Kaphaj yonivyapad (i.e. trichomoniasis) is 8.5%.

Ayurvedic treatment for the management of Kaphaj yonivyapad could be safe, effective, readily available and with less side effect.

For the management of Kaphaj yonivyapad both oral and local medication would have great impact.Since no work has been done on Palashadi Churna Orally in Kaphaj Yonivyapad With Special Reference To Trichomonas Vaginitis and no comparative has been conducted out. So it will help to fill knowledge gap.

Including the married female patient having sign and symptoms of Kaphaj Yonivyapad like P/V discharge, Itching and pain at vulval site between age group of 18-49 year who fulfill clinical diagnostic criteria. Written consent is taken from patient to ensure ethical compliance and transparency in research process. Sample size calculated is 35 in each group by using formula by Daniel 1999. Simple random sampling technique will be used. Total 70 number of patients will be divided in two group named as Group A (trial group and Group B (control group). Palashadi churna orally to group A (Trial group), Pippalyadi churna orally to group B (control group) will be given to patients. Guduchyadi Yonidhawan will be given to both groups. Drugs will be purchased from GMC certified pharmacy. Both drugs will be administered for 7 days. All SOP of Churna preparation and kawatha preparation and Yonidhawan  procedure will be followed throughout the clinical trial. Observation will be done on 0th and 7th day of treatment. Follow will be taken on 14th day

Result will be drawn on basis of assessment criteria and statistical analysis. Discussion will be done on the basis of observation and result obtained during treatment. Summary will be drawn out.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant Blinded

入排标准

年龄范围
18.00 Year(s) 至 49.00 Year(s)(—)
性别
Female

入选标准

  • Married Patients Having Symptoms Of Kaphaj Yonivyapada i.e. Vaginal Discharge Pruritis Vulvae Dull pain.

排除标准

  • Unmarried, Pregnant, Post-natal Women.
  • Infections Like Syphilis, HIV, Herpes Genitalia.

结局指标

主要结局

Reduction In Signs And Symptoms Of Kaphaj Yonivyapad After Taking Palashadi Churna Orally And Guduchyadi Kwath Yonidhwana.

时间窗: 7 days

次要结局

  • When The Trial Group Stands In Comparison With Control Group.(18 months)

研究者

发起方
Dr Nupura Dilip Lakhan
申办方类型
Other [self]

研究点 (1)

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