CTRI/2024/11/076555尚未招募3 期
A Comparative Pharmaceutical Study Of Amritadi Ghrita Prepared by Desi Cow Milk and Jersey Cow Milk and Its Effect on Vatarakta With Special Reference To Gout
GOVERNMENT PG AYURVEDIC COLLEGE AND HOSPITAL1 个研究点 分布在 1 个国家目标入组 60 人开始时间: 2024年12月3日最近更新:
试验速览
- 阶段
- 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
- Improvement in reduction of increased Uric acid and Symptomatic relief
研究概览
简要总结
This study is interventional study trial, comparing the efficacy of AMRITADI GHRITA in gout which is prepared by two different media.
Patient will be randomly selected from OPD of department of Rasa shastra and Bhaishajya Kalpana and Kayachikitsa, at government P.G ayurvedic college and hospital, Varanasi.
60 patients will be studied under 2 group; having 30 patients in each group.
Group -A - 30 patients will be treated by AMRITADI GHRITA prepared by Desi cow milk.
Group -B - 30 patients will be treated by AMRITADI GHRITA prepared by Jersey cow milk.
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 60.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients of either gender in the age group between 20-60 years.
- •Patients who fulfilled the diagnostic criteria.
- •Patients who have serum uric acid level more than 7mg/d in males and more than 6mg/dl in females with or without any associate feature like joint pain and inflammation.
- •Disease presenting with classical clinical feature of Vatarakta like, Sandhi shool (Joint pain), Sandhi shotha (Swelling of joint), Sparsha asahatvam (Tenderness), Raga (Redness), Twak vaivarnya (Discolouration of skin) and Vidaha(Burning sensation).
- •Patients who are willing to participate in trial.
排除标准
- •Patients who are not willing to participate in trial.
- •Patients below the age of 20 years and above 60 years of age.
- •Patient having chronic symptoms of Vatarakta along with other deformities.
- •Patients who are suffering from any other form of arthritis like Osteoarthritis, Tubercular Arthritis, Rheumatoid Arthritis etc.
- •Patients who are suffering from chronic renal, respiratory, cardiac or hepatic disorder.
- •Patients who have any malignancy.
- •Patients who are pregnant and lactating mother.
结局指标
主要结局
Improvement in reduction of increased Uric acid and Symptomatic relief
时间窗: Within 14 days
次要结局
- Normal level of Uric acid & complete symptomatic relief(With in 30 days)
研究者
DR PURAN UPADHYAY
Government P.G Ayurvedic College And Hospital
研究点 (1)
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