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临床试验/JPRN-UMIN000001762
JPRN-UMIN000001762已完成未知

Effects of Telmisartan compared with Candesartan on ischemic cardiovascular events in high-risk hypertensive patients: a multi-center, prospective, randomized, open-labeled, blinded endpoints trial - Effects of Telmisartan on ischemic cardiovascular events in high-risk hypertensive patients: a multi-center, prospective, randomized, open-labeled, blinded endpoints trial

Department of Cardiovascular Medicine, Kyoto Prefectural University School of Medicine0 个研究点目标入组 1,500 人开始时间: 2009年4月1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
1,500

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
30years-old 至 85years-old(—)
性别
All

入选标准

  • 未提供

排除标准

  • The exclusion criteria are set as follow: 1.History of worsening of heart failure within the preceding 6 months 2.Planned elective percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) within the anteceding 3 months 3.History of myocardial infarction, unstable angina pectoris, percutaneous coronary intervention (PCI) or coronary artery bypass grafting (CABG) within the preceding 12 months 4.History of percutaneous hind limb angioplasty (PTA) or bypass grafting within the preceding 6 months 5.History of cerebral infarction, cerebral hemorrhage within the past 6 months 6.Congenital heart disease 7.Uncontrolled hypertension on treatment (eg, BP>180/110 mmHg) 8.Pregnant women or women of childbearing potential 9.Hepatic dysfunction (AST or ALT >100IU/L) 10.Renal impairment (serum creatinine level >2.0 mg per 100 ml) 11.Known hypersensitivity or intolerance to ARB

研究者

发起方
Department of Cardiovascular Medicine, Kyoto Prefectural University School of Medicine

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