CTRI/2024/12/077754尚未招募2/3 期
A clinical study of the effect of Simhasyadi kwatha in the management of Hyperuricemia.
Dr Aditi Acharya1 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17日最近更新:
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
- To asses the effectiveness of SIMHASYADI KWATHA in management of symptomatology of Hyperuricemia.
研究概览
简要总结
This is a clinical study of SIMHASYADI KWATHA in management of Hyperuricemia. This study is done as a mandatory Post graduation thesis work. Total number of 60 patients will be studied for 60 days each.
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
- •1.Patients of both the sex and age between 20-70 years.2.Naive patients or newly diagnosed patients of Hyperuricemia.3.Patients having serum uric acid more than 6.9mg/dl.
- •Patients of Hyperuricemia with Gouty Arthritis.5.Patient recently diagnosed with uncomplicated Hyperuricemia & Gouty Arthritis.6.Hyperuricemic patients suffering from controlled hypertension, diabetes mellitus, CKD upto stage 3.
排除标准
- •1.Asymptomatic patient with Hyperuricemia.
- •2.Patients suffering from the complications of Hyperuricemia & Gouty Arthritis.
- •3.Pregnant and lactating women.
- •4.Presence of disease like CA, HIV, malignant hypertension, uncontrolled diabetes.
- •Patients suffering from major systemic illness or under long term drug treatment.
结局指标
主要结局
To asses the effectiveness of SIMHASYADI KWATHA in management of symptomatology of Hyperuricemia.
时间窗: 45 days
次要结局
- To compare the effect of SIMHASYADI KWATHA and FEBUXOSTAT on serum uric acid level parameter.(30, 45 and 60 days)
研究者
Dr Aditi Acharya
Govt Ayurvedic College and Hospital Guwahati
研究点 (1)
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