An Open-label, single center, Non – Interventional, Observational Studyto Evaluate Efficacy and safety of Herbal nutritional Supplement(Cuminum cyminum, Zingiber officinale, Myristica fragrans, Elettariacardamomum, Linum usitatissimum, Psidium guajava ,Curcuma longa,Cinnamomum verum, Syzygium aromaticum, Glycyrrhiza glabra,Trigonella foenum-graecum, Foeniculum vulgare, Nigella sativa) inmanagement of hypertension and its associated risk factors
试验速览
- 阶段
- 4 期
- 状态
- 尚未招募
- 发起方
- 入组人数
- 50
- 试验地点
- 1
- 主要终点
- efficacy of suppliment in 60 days in hypertesive patients and its management with basic parameters
研究概览
简要总结
This is a Non –Interventional Observational study. After obtaining informed consent frompatient for study participation, the doctor will prescribe the herbal nutritionalsupplement as part of routine clinical practice based on the doctor’sknowledge and experience. After four weeks of treatment the patient will be requested tovisit the hospital for follow-up.
Atotal of 50 (25- subjects newhypertensive i.e <1 Year with HTN; 25 subjects with long term Hypertensivei.e >1 year with HTN) subjects with age group >45years and surviving with standard medication should be considered to initiate treatment with Herbal nutritionalSupplement(Cuminum cyminum, Zingiber officinale, Myristica fragrans, Elettariacardamomum, Linum usitatissimum, Psidium guajava ,Curcuma longa, Cinnamomumverum, Syzygium aromaticum, Glycyrrhiza glabra, Trigonella foenum-graecum,Foeniculum vulgare, Nigella sativa) for a period of 6 months to stusy the effucacy of the herbal suppliment in mange ment of hypertension
研究设计
- 研究类型
- Observational
入排标准
- 年龄范围
- 40.00 Year(s) 至 70.00 Year(s)(—)
- 性别
- All
入选标准
- •Male and female treatment naïve patients, aged >45 years, with diagnosis of hypertension (DBP 110 mm Hg and SBP >150mm Hg).
排除标准
- •Male and female treatment naïve patients, aged <45 years, with diagnosis of hypertension (.
结局指标
主要结局
efficacy of suppliment in 60 days in hypertesive patients and its management with basic parameters
时间窗: 30 days from the enrollment day
次要结局
- efficacy of suppliment in 60 days in hypertesive patients and its management with parameters(8)
