JPRN-UMIN000003684已完成未知
A comparison of twenty-four-hour blood pressure control between candesartan and other ARBs estimated by the ambulatory blood pressure monitoring - Effect of candesartan on 24-hours blood pressure control
Department of Integrated Medicine, Ehime University Graduate Schoolof Medicine0 个研究点目标入组 50 人开始时间: 2010年6月19日最近更新:
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 发起方
- 入组人数
- 50
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 20years-old 至 80years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1. secondary hypertension 2. systolic blood pressure >160 mmHg and or diastolic blood pressure > 100 mmHg 3. malignant hypertension 4. history of stroke, myocardial infarction and other cardiovascular disease that needed hospitalization within recent 6 months. 5. atrial fibrillation 6. patients with fundal hemorrhage, exudation or papilledema due to hypertensive retinopathy 7. liver dysfunction(the levels of AST or ALT reached 250% of their upper normal limit.) 8. Renal dysfunction (serum creatinine > 2.0 mg/dl) 9. hyperkalemia (serum K > 5.5 mEq/l) 10. pregnant or nursing women 11. patients who are not recommended for participation in this study by physician in charge with medical reasons.
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