NCT00767247终止不适用
Analysis of Antihypertensive Treatment Efficacy
适应症
试验速览
- 阶段
- 不适用
- 状态
- 终止
- 发起方
- AstraZeneca
- 入组人数
- 2,000
- 试验地点
- 1
- 主要终点
- Analysis of antihypertensive treatment efficacy.
研究概览
简要总结
Analysis of antihypertensive treatment efficacy.
研究设计
- 研究类型
- Observational
- 观察模型
- Case Control
- 时间视角
- Prospective
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
- •arterial hypertension
- •intake of Atacand before study enrollment
排除标准
- •hypersensitivity to candesartan or any other ingredient of Atacand
- •liver function impairment and/or cholestasis
- •severe renal insufficiency (serum creatinine > 265 µmol/L)
- •Pregnant and lactating women
结局指标
主要结局
Analysis of antihypertensive treatment efficacy.
时间窗: measurement BP: 3 visits for 3 month
次要结局
未报告次要终点
研究者
研究点 (1)
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