A Randomized Controlled Clinical Study to Evaluate the Efficacy of Hinguvachadi gutika and tablet Mefanamic acid and Dicylomine in the management of Kashtaarthva.
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Decrease in pain, duration and intensity
研究概览
简要总结
The study will be intervened by the treatment of HIngu-vachadi Gutika and tab Mefanamic acid and Dicylomine to group A and group B respectively. The efficacy of the therapy will be assessed on the basis of subjective criteria for statistical analysis. Scoring will be designed according to the severity of symptoms. The subjective gradation of symptoms will be done as follows and the intensity of each symptom will be calculated before treatment, after treatment and after follow up. The effect of treatment result will be assessed in regards to clinical signs and symptoms on the basis of grading and scoring system. The signs and symptoms will be assessed by adopting the suitable scoring method
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- None
入排标准
- 年龄范围
- 18.00 Year(s) 至 35.00 Year(s)（—）
- 性别
- Female
入选标准
- •All the women unmarried or married complaining of painfull menstruration at least 3 consecutive cycle.
排除标准
- •Known Cases of secondary dysmenorrhea with pelvic pathology prolapse ,uterine fibroid, pelvic endometriosis, cervical stenosis ,Pelvic inflammatory Diseases.
- •Participant with intrauterine contraceptive device 3) Participant is on hormonal therapy.
结局指标
主要结局
Decrease in pain, duration and intensity
时间窗: 3 days
次要结局
- Decrease in pain, duration, clots and intensity(5 days)
研究者
Dr Mayur Pratapsing Ingale
Tilak Ayurved Mahavidyalaya