跳至主要内容
临床试验/CTRI/2024/05/067277
CTRI/2024/05/067277尚未招募2 期

Comparative clinical study to evaluate the efficacy of Dashamoola Ksheera Paka and Rajapravartini Vati followed by Matrabasti in Udavartini Yoni Vyapath w.s.r Primary Dysmenorrhoea

Dr Lakshmi D R1 个研究点 分布在 1 个国家目标入组 120 人开始时间: 2024年5月25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
120
试验地点
1
主要终点
1.Dashamoola Ksheera paka followed by Moorchita taila matra basti is not effective

研究概览

简要总结

A Comparative Clinical Study to Evaluate the Efficacy of Dashamoola ksheera Paka and Rajapravartini Vati followed by Matra Basti in Udavartini Yoni Vyapath W.S.R To Primary Dysmenorrhoea - A Sample size of 100 patients, 2 group with random allocation.

Group A : Dashamoola Ksheera Paka 50 ml BD followed by Matrabasti (60ml) for 5 days before commencement of Menstrual Cycle and

Group B : Rajapravartini vati 250mg BD followed by Matrabasti (60ml) for 5 days before commencement of Menstrual Cycle and  for 3 consecutive cycles.

results will assessed statistically.

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
11.00 Year(s) 至 30.00 Year(s)(—)
性别
Female

入选标准

  • 1.Age Group Menarche to 30 years 2.Patients with "Pratyatma Lakshana" of Udavartini Yoni Vyapath 3.patient who are willing to participate in our treatment.

排除标准

  • Patients with Chronic general illness and Systemic disorders. 2.Patients with intrauterine contraceptive devices, oral contraceptives. 3.Any Congenital anomalies 4.Any uterine pathology.
  • fibroid, Adenomyosis, endometriosis, PID, Menorrhagia etc.

结局指标

主要结局

1.Dashamoola Ksheera paka followed by Moorchita taila matra basti is not effective

时间窗: 3 months

in Udavartini Yoni Vyapath.

时间窗: 3 months

2.Dashamoola Ksheera paka followed by Moorchita taila matra basti is effective in Udavartini Yoni Vyapath

时间窗: 3 months

3.Rajapravartini Vati followed by Murchita taila matra Basti is not effective in Udavartini Yoni Vyapath

时间窗: 3 months

4.Rajapravartini Vati followed by Murchita taila matra Basti is effective in Udavartini Yoni Vyapath.

时间窗: 3 months

次要结局

未报告次要终点

研究者

发起方
Dr Lakshmi D R
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

DR Lakshmi D R

N K Jabshetty Ayurvedic Medical College & P G Center Bidar

研究点 (1)

Loading locations...

相似试验