Clinical evaluation of sarpagandha ghanvati in hypertension
试验速览
- 阶段
- 2 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 40
- 试验地点
- 1
- 主要终点
- a) Headache
研究概览
简要总结
This study is a open label clinical trial to determine the efficacy of sarpagandha ghanvati in hypertension for the age group between 18 to 70 years for 45 days.Study will be conducted at UAU, Gurukul Campus, Haridwar on 40 patients. Assessment will be done on the basis of subjective and objective parameters. Study will be conducted at OPD/IPD level of PG department of Kayachikitsa. Assessment will be done at weekly interval and result obtained will be analyzed using appropriate tests
研究设计
- 研究类型
- Interventional
- 分配方式
- Not Applicable
- 盲法
- Open Label
入排标准
- 年龄范围
- 18.00 Year(s) 至 70.00 Year(s)（—）
- 性别
- All
入选标准
- •Patients of either sex with age between 18-70 years Patients having Systolic Blood Pressure is more than 140 and less than 180 mm of Hg Patients having Diastolic Blood Pressure is more than 90 and less than or equal to 110 mm of Hg.
排除标准
- •Patients of either sex below 18 years & above 70 years will be excluded from the study Patients having Systolic Blood Pressure is more than 180mm of Hg Patients having Diastolic Blood Pressure is more than 110mmHg Patients suffering from serious comorbidities like Renal failure, Coronaryartery disease, endocrinal disorder, congestive heart disease Pregnant woman.
结局指标
主要结局
a) Headache
时间窗: Assessment willl be done weekly for 8 weeks
b) Giddiness
时间窗: Assessment willl be done weekly for 8 weeks
c) Palpitations
时间窗: Assessment willl be done weekly for 8 weeks
d) Breathlessness
时间窗: Assessment willl be done weekly for 8 weeks
e) Insomnia
时间窗: Assessment willl be done weekly for 8 weeks
次要结局
- 1. systolic blood pressure(2. diastolic blood pressure)