Pharmaceutico analytical study and clinical efficacy of Vriddhadarvadya lauha in Amavata wsr to Rheumatoid Arthritis
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 60
- 试验地点
- 1
- 主要终点
- Change in RA factor and CRP reading
研究概览
简要总结
This study is A Pharmaceutico - Analytical Study And Clinical Efficacy of Vriddhadarvadya Lauha in Amavata wsr to Rheumatoid arthritis . There will be 2 groups in the study, In Group A randomly selected and clinically diagnosed 30 patients of Amavata whose RA Factor and CRP will be high than normal range.Group A will be given prepared Vriddhadarvadya Lauha as per classical method and 30 patients of Group B randomly selected and clinically diagnosed will be placebo group. Trial will be conduct for a period of 2 months. Follow up of the case will be after every 15 days that is 4 times during treatment. Final assessment will be done after completion of 2 months course on the basis of subjective, objective and laboratoral assessment. The data will be analyzed scientifically and statistically.
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- None
入排标准
- 年龄范围
- 20.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Amavata signs and symptoms morning stiffness tenderness and swelling of joints ete Results of lab tests showing RA factor and CRP test Patients between the ages of 20 yrs to 70 yrs.
排除标准
- •Patients having severe deformity and complications patients suffering from serious illnesses like cancer chronic liver failure etc Pregnant and lactating women A patient with any drug sensitivity Patients age below 20 yrs and above 70 yrs.
结局指标
主要结局
Change in RA factor and CRP reading
时间窗: 2 months
次要结局
- RA factor and CRP will be assessed(15 days,30 days & 45 days)
研究者
Dr Ankita Kumawat
Madan Mohan Malviya Goverment Ayurveda College Udaipur