JPRN-UMIN000003417已完成未知
Efficacy and safety of switching from angiotensin II receptor blocker-diuretic combinations therapy to combination tablets (candesartan cilexetil-hydrochlorothiazide) in hypertension. - BLOARD study
适应症
试验速览
- 阶段
- 未知
- 状态
- 已完成
- 入组人数
- 70
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 90years-old（—）
- 性别
- All
入选标准
- 未提供
排除标准
- •1.Patient who is anuric and/or dialysis 2.Patient with ARF (acute renal failure) 3.Patient with sodium - and potassium - depletion / sodium - and potassium - depleted patients 4.Patient who is pregnant or possibly pregnant 5.Patients with a history of hypersensitivity to ingredients of Ecard HD (candesartan cilexetil-hydrochlorothiazide) or other thiazide or thiazide-like diuretics 6.Patient who is determined to be excluded from the study due to any reason by the study doctor
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