EUCTR2007-007026-22-CZ进行中（未招募）不适用
Assessment of the effects on 24-hour ambulatory blood pressure and the safety of a once-a-day oral 8 mg perindopril morning administration versus evening administration in hypertensive patients. An 8-week, 2-arm, randomised, double-blind study.
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中（未招募）
- 入组人数
- 500
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Essential hypertension after institution of appropriate healthy lifestyle modification, measured with a validated automatic measurement device in the medical office in supine position: 95 = DBP < 110 mmHg and SBP < 180 mmHg.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) yes
- •F.1.3.1 Number of subjects for this age range
排除标准
- •Kalaemia = local laboratory's high normal values
- •Positive pregnancy test for non menopausal women
- •Creatinine = 150 mmol/l or creatinine clearance < 60 ml/mn, using Cockroft's formula
研究者
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