NCT01295021已完成不适用
A Non Interventional, Cross Sectional, Study on the Prevalence of Sympathetic Overactivity in Hypertensive Patients.
适应症
试验速览
- 阶段
- 不适用
- 状态
- 已完成
- 发起方
- AstraZeneca
- 入组人数
- 1,514
- 试验地点
- 1
- 主要终点
- Prevalence of SO in newly diagnosed hypertensive patients
研究概览
简要总结
The purpose of this NIS is to assess the prevalence of sympathetic overactivity in patients with newly diagnosed essential hypertension.
详细描述
MC MD
研究设计
- 研究类型
- Observational
- 观察模型
- Cohort
- 时间视角
- Cross Sectional
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Newly diagnosed essential hypertension patients will be eligible for the study.
- •Average of two or more systolic BP readings ≥ 140mmHg or diastolic BP readings ≥ 90mmHg
排除标准
- •History of coronary artery disease
- •History of diabetes
结局指标
主要结局
Prevalence of SO in newly diagnosed hypertensive patients
时间窗: Visit 1-3: heart rate & Blood pressure, treatment presribed by physician. The interval between visit 1 and visit 2 is upto 4 weeks and interval between visit 2 & visit 3 is upto 4 weeks depending on Investigators discretion.
次要结局
- Association of SO and heart rate.(Visits 1-3)
- Subjective symptoms noticed by the doctor.(1st visit)
- To record the drugs used in the treatment of patients diagnosed with hypertension.(Visits 1-3)
研究者
研究点 (1)
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