CTRI/2022/10/046583尚未招募2/3 期
Randomised clinical trial to study efficacy of Eranda Sneha(5ml)with Shunthi Kwatha(50ml) in the management of Katishoola with special reference to Chakradatta.
试验速览
- 阶段
- 2/3 期
- 状态
- 尚未招募
- 入组人数
- 35
- 试验地点
- 1
- 主要终点
- Primary outcome is assessment of Katishoola with pain scale
研究概览
简要总结
The study will be done on the patients selected on the basis on inclusion criteria, The initial assessment will be done on 1st day. Then the treatment will be started (Erand sneha 5ml with sunthi kwatha 50ml before dinner for seven days. On 8th day follow up will be done. Result of 1st day assessment will be compared with 8th day assessment. Result will be drawn after discussion and conclusion based on statistical analysis
研究设计
- 研究类型
- Interventional
- 分配方式
- Random Number Table
- 盲法
- Open Label
入排标准
- 年龄范围
- 30.00 Year(s) 至 60.00 Year(s)（—）
入选标准
- •1.Patients having symptom of Katishool more than 7 days and less than 3 months. 2.Avarodha Janya Samprapti. 3.No specific and major pathology of degenerative changes
- •Male and Female.
排除标准
- •1.Taking NSAIDs 2.Patient having inborn structural deformities.
- •Diagnosed with Fracture of Lumbar Spine etc.
- •and needs surgical intervention 4.Patients having other joint deformities or diseases which are not related to Katishoola.
- •Katishoola is associated with known case of Cardiac disease, Pulmonary TB, Pregnancy, Paralysis, Neurological disorder, HIV or any other relevant pathology.
结局指标
主要结局
Primary outcome is assessment of Katishoola with pain scale
时间窗: intervention for consecutive 7 days
次要结局
- Comparative analysis of pain and functional improvement
研究者
研究点 (1)
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