A Randomized Control Trial To Compare Efficacy Of Dashmool Rasayana And Chitraka Haritaki In The Management Of Vataj Pratishaya
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 150
- 试验地点
- 1
- 主要终点
- Primary outcome is improve the patient quality of life by reducing impact of disease on their daily activities
研究概览
简要总结
This study is RANDOMIZED CONTROL TRIAL TO COMPARE EFFICACY OF DASHMOOL RASAYANA AND CHITRAKA HARITAKI IN THE MANAGEMENT OF VATAJ PRATISHAYA
Total 150 Patients of age 15 years to 50 years of both sex will be randomly selected for this clinical trial and divided into two groups
Group A – Total 75 Patients
These patients will be treated with Dashmool rasayan
Route of administration – Rasayan sewan (Orally)
Time of administration – Rasayan sewan kal
Group B – Total 75 Patients
These patients will be treated with Chitraka haritaki
Route of administration – (Orally)
Time of administration – ( twice a day)
Data will be analysed and appropriate statistical test will be applied
研究设计
- 研究类型
- Interventional
- 分配方式
- Coin toss, Lottery, toss of dice, shuffling cards etc
- 盲法
- Participant Blinded
入排标准
- 年龄范围
- 15.00 Year(s) 至 50.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients Having Sign and Symptoms of Vataj Pratishaya.
排除标准
- •Patient not willing for written consent.
- •Patient suffering from any Systemic disorders like DM, HTN, HIV, HbsAg .
- •Patient with chronic infective respiratory disease like pneumonia etc and nasal tumors.
结局指标
主要结局
Primary outcome is improve the patient quality of life by reducing impact of disease on their daily activities
时间窗: 60 days
次要结局
- Adverse reaction if any(60 days)