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临床试验/CTRI/2025/02/079885
CTRI/2025/02/079885尚未招募1 期

A Randomized Comparative Clinical study to Evaluate the efficacy of vachadi churna and Chaturbeeja churna in the management of Udavartini Yonivyapada w.s.r to Primary Dysmenorrhoea

Dr Pooja Nivrutti Ugalmugale1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2025年2月3日最近更新:

试验速览

阶段
1 期
状态
尚未招募
发起方
入组人数
40
试验地点
1
主要终点
Assessment will be done before and after treatment as per the parameters

研究概览

简要总结

The Present Title A Randomised Comparative Clinical study to evaluate the efficacy of vachadi churna and chaturbeeja churna in the management of UDAVARTINI YONIVYAPADA WITH SPECIAL REFERENCE TO PRIMARY DYSMENORRHOEA

Duration of treatment 7 Days starting from 21st days of menstrual cycle and this for 3 consecutive cycles

Patients will be examined before starting the treatment  In bleeding phase of the previous cycle on 5th day of 1st 2nd 3rd cycle after treatment

Group A will be administered with vachadi churna 12 gm per day in 2 divided doses with koshnjal

Group B will be administered with chaturbeeja churna 12 gm per day in 2 divided doses

Assessment will be done with subjective objective criteria

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
14.00 Year(s) 至 25.00 Year(s)(—)
性别
Female

入选标准

  • Patients with Hb of more than 10 g/dl Patients diagnosed as primary dysmenorrhoea Having regular menstrual cycles Patients complaining of painful menstruation for at least two consecutive cycles.

排除标准

  • Patients having congenital anomalies leading to dysmenorrhoea.
  • Patients having any pelvic pathology.
  • Patients with uterine fibroid.
  • Known Case of PCOD.
  • Known Case of Congenital Heart Diseases HTN,DM,TB etc Patients diagnosed as secondary dysmenorrhoea.

结局指标

主要结局

Assessment will be done before and after treatment as per the parameters

时间窗: 7 days for 3 consecutive cycles

Subjective criteria vedana-Intensity Duration site Nature

时间窗: 7 days for 3 consecutive cycles

Artavpravrutti Nausea vomiting fatigue

时间窗: 7 days for 3 consecutive cycles

Objective criteria FLA Scale Tenderness

时间窗: 7 days for 3 consecutive cycles

次要结局

  • Tenderness(Face leg activity scale)

研究者

发起方
Dr Pooja Nivrutti Ugalmugale
申办方类型
Other [self]
责任方
Principal Investigator
主要研究者

Dr Pooja Nivrutti Ugalmugale

Dr.N.A.Magadum Ayurvedic medical college, Hospital and Research centre Ankali-591213

研究点 (1)

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