A Clinico-Comparative study of Kakubhadi Churna and Rasayana Vati, in he management of Raktagatavata with special reference to Essential Hypertension
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
- during this trial patients will be assessed on following parameters
研究概览
简要总结
this study is a randomised interventional clinical trial to evaluate the efficacy of Kakubhadi Churna and Rasayana Vati in the management of Raktagatavata w.s.r. to Essential hypertension. Total no. of patients 60 will be enrolled in present study. selected patients will be divided into 3 groups on the basis of computer generated randomization method.
group A 20 patients will be given Rasayana vati 2 tablets twice a day with lukewarm water
group B 20 patients will be given kakubhadi churna 3 gm twice a day with lukewarm water
group C 20 patients will be given both Rasayana vati and Kakubhadi churna twice daily with lukewarm water
研究设计
- 研究类型
- Interventional
- 分配方式
- Computer generated randomization
- 盲法
- Open Label
入排标准
- 年龄范围
- 20.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •patients presenting with classical sign and symptoms as described in ayurvedic and modern medicine.
排除标准
- •1 endocrine disease 2 renal disease 3 hypertension with cerebral complications 4 cerebral hemorrhages, convulsive seizures
- •toxemia of pregnancy 6 poisoning 7 pre eclampsia.
结局指标
主要结局
during this trial patients will be assessed on following parameters
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
subjective criteria
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
systolic blood pressure
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
dizziness
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
excessive sweating
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
diastolic blood pressure
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
headache
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
palpitation
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
edema
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
epitaxis
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
objective criteria
时间窗: 1)At the baseline day | 2)after completion of trial i.e after 2 months | 3) total study period of 15 months
次要结局
未报告次要终点