Efficacy of balaguduchyadi taila matra basti in comparison to sahacharadi taila matra basti in udavartini yoni vyapat - dysmenorrhea - a randomized clinical trial
试验速览
- 阶段
- 2/3 期
- 状态
- 招募中
- 发起方
- 入组人数
- 30
- 试验地点
- 1
- 主要终点
- Improvement in Pain as assessed by DVPRS scale
研究概览
简要总结
Efficacy of Balaguduchyadi taila matra basti in comparison to Sahacharadi taila matrabasti in comparison to Udavartini yonivyapat- Dysmenorrhea - A Randomised clinical study. In my study i have taken 2 groups. Group1 is of trial drug Balaguduchyadi taila matra basti and Group 2 is of control drug Sahacharadi taila matrabasti. Medicine will be selected by computer cheat methods. Here both the participant and investigator will know the drug which is selected. Duration of procedure is 7 days after 48 hours of cessation of menstruation and follow-up will be done for 2 consecutive menstrual cycles, total duration of study is 3 menstrual cycles. Methodology is Interventional(clinical) for study group- 18-35 years old female patients with featiures of Udavartini yoni vyapat-Dysmenorrhea attending Prasooti tantra evan Stri roga out-patient department in Shri Dharmasthala Manjunatheshwara Institute of Ayurveda College and Hospital, Bangalore.Methodology is Interventional(clinical) for control group- 18-35 years old female patients with featiures of Udavartini yoni vyapat-Dysmenorrhea attending Prasooti tantra evan Stri roga out-patient department in Shri Dharmasthala Manjunatheshwara Institute of Ayurveda College and Hospital, Bangalore.
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
- 18.00 Year(s) 至 35.00 Year(s)(—)
- 性别
- Female
入选标准
- •Both married and unmarried women with painful menstruation without pelvic pathology, Patients with age between 18 to 35 years, Patients fulfilling the diagnostic criteria.
排除标准
- •Congenital anomalies of genital tract, Dysmenorrhea with pelvic pathology- Fibroid uterus, ovarian cyst, Malignancy, IUCD; Patients with any Systemic Diseases- DM, HTN, TB; Rectal pathologies like haemorrhoids, fissure, fistula; Patients with diarrhea.
结局指标
主要结局
Improvement in Pain as assessed by DVPRS scale
时间窗: At baseline, 7th day, 37th day and 67th day
Decrease in severity of Udavartini yonivyapat- dysmenorrhea based on VMSS scale.
时间窗: At baseline, 7th day, 37th day and 67th day
次要结局
- Improvement in quality of life by reducing the signs and symptoms of Udavartini yonivyapat- dysmenorrhea.(3 months)
研究者
Dr M B Chinamayee
SDM Institute of Ayurveda College and Hospital, Anchepalya, Kumbalagodu post, Bangalore
