CTRI/2022/10/046617尚未招募4 期
A comparative clinical study to evaluate the effect of Pathyadi churan and Shunthyadi kwatha in the management of Amavata w.s.r. to Rheumatoid Arthritis
Rajiv Gandhi Govt Post Graduate Ayurvedic College and Hospital Paprola1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2022年10月30日最近更新:
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 20
- 试验地点
- 1
- 主要终点
- Relief in symptoms of Amavata after intervention of pathyadi churana and shunthayadi kwatha
研究概览
简要总结
patients will be selected from faculty/OPD of RGGPG Ayurvedic College and Hospital, Paprola. Two groups of 10 patients will be selected on the basis of inclusion and exclusion criteria. Interventional drug will be given to both groups of patient to know the effect of kwatha and churna
研究设计
- 研究类型
- Interventional
- 分配方式
- Other
- 盲法
- Not Applicable
入排标准
- 年龄范围
- 30.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients willing for study.
- •Patients in the age group between 30-70 years, irrespective of sex and socio-economic status.
- •Patient with signs and symptoms of Amavata w.s.r. to Rheumatoid Arthritis as described in texts and fulfill the diagnostic criteria.
排除标准
- •Patients not willing for the trial Patients with age group below 30 and above 70 years.
- •Allergy to the trial drug.
- •Patients having any type of arthopathy such as neoplasm of spine,ankylosing spondylosis, osteoarthritis, traumatic arthritis and pyogenic osteomyelitis etc.
- •Patients suffering from chronic renal, respiratory, cardiac and hepatic .
- •Pregnant and lactating women.
结局指标
主要结局
Relief in symptoms of Amavata after intervention of pathyadi churana and shunthayadi kwatha
时间窗: 6 weeks
Angamarda
时间窗: 6 weeks
Aruchi
时间窗: 6 weeks
Trishna
时间窗: 6 weeks
Alsaya
时间窗: 6 weeks
Apaka
时间窗: 6 weeks
Gaurava
时间窗: 6 weeks
Jwara
时间窗: 6 weeks
Sandhishoola
时间窗: 6 weeks
Sandhishotha
时间窗: 6 weeks
Sparshasahtva
时间窗: 6 weeks
Vibandha
时间窗: 6 weeks
Antrakujana
时间窗: 6 weeks
Nidraviparyaya
时间窗: 6 weeks
Praseka Daha
时间窗: 6 weeks
次要结局
- Improving quality of life(6 weeks)
研究者
研究点 (1)
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