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临床试验/CTRI/2025/07/090374
CTRI/2025/07/090374招募中2 期

A Comparative clinical evaluation of effect of apamarga kshara and tagaradi taila yonipichu in the management of karnini yonivyapad w.s.r to cervical erosion

State Ayurvedic College and Hospital,Tulsidas marg, Turiyaganj, Lucknow, Uttar Pradesh, India1 个研究点 分布在 1 个国家目标入组 45 人开始时间: 2025年7月21日最近更新:

试验速览

阶段
2 期
状态
招募中
发起方
入组人数
45
试验地点
1
主要终点
1.To evaluate the efficacy of Apamarga kshara in the management of karnini yonivyapad.

研究概览

简要总结

This is a Randomised, comparative clinical study Phase 2 Parallel group trial. Comparing the efficacy of Apamarga kshara and Tagaradi taila yonipichu in cases of Karnini Yonivyapad for 2 months in 45 patients. The patient fulfilling the clinical criteria for diagnosis of Karnini Yonivyapad will be randomly selected from OPD/IPD of State Ayurvedic College and Hospital, Lucknow and referred cases from other hospitals. A careful history, physical examination and necessary investigation will be performed. Further patient divided into three groups, Group-A- In this group patients will be treated with Apamarga kshara locally on cervix for 3 sittings for 2 consecutive cycles. Group-B- In this group patients will be treated with Tagaradi taila yonipichu locally for one week after cessation of menses for 2 consecutive cycles. Group-C-In this group patients will be treated with Apamarga kshara locally on cervix once a week along with Tagaradi taila yonipichu locally for one week  after cessation of menses for 2 consecutive cycles .Follow up period- 7 days during the treatment and 7days after the completion of trial.

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
22.00 Year(s) 至 45.00 Year(s)(—)
性别
Female

入选标准

  • 1.Patients present with the sign and symptoms of karnini yonivyapada ( cervical erosion) and clinically confirmed on per speculum examination .
  • 2.Age between 22 to 45 years.
  • 3.Married women.
  • 4.Erosion covering more than 25 % area of cervix.
  • 5.Persistent leucorrhea, pelvic pain, backache, contact bleeding.
  • 6.Patients willing to through trial.

排除标准

  • 1.Unmarried women.
  • 2.Pregnant women, lactating women, women on OCP & PID.
  • 3.Women of age less than 22 and above than 45 Years.
  • 4.Other systemic disorders like hypertension, diabetes, tuberculosis.
  • 5.Patient having any malignant growth.
  • 6.HIV, VDRL, HBsAg positive patient.

结局指标

主要结局

1.To evaluate the efficacy of Apamarga kshara in the management of karnini yonivyapad.

时间窗: 1. At interval of 7 days | 2. Daily for 7 days | 3. At interval of 7 days and daily for 7 days

2.To evaluate the efficacy of Tagaradi taila yonipichu in the management of karnini yonivyapad.

时间窗: 1. At interval of 7 days | 2. Daily for 7 days | 3. At interval of 7 days and daily for 7 days

3.To compare the efficacy of Apamarga kshara with Tagaradi taila yonipichu in the management of karnini yonivyapad.

时间窗: 1. At interval of 7 days | 2. Daily for 7 days | 3. At interval of 7 days and daily for 7 days

次要结局

  • 1.Conceptual study of Karnini Yonivyapad and its modern correlation.(2.To find the safe and potent drug for Karnini Yonivyapad.)

研究者

发起方
State Ayurvedic College and Hospital,Tulsidas marg, Turiyaganj, Lucknow, Uttar Pradesh, India
申办方类型
Government medical college
责任方
Principal Investigator
主要研究者

Dr Sanju Lata Patel

State Ayurvedic college and Hospital, Tulsidas marg, Turiyaganj, Lucknow

研究点 (1)

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