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临床试验/JPRN-UMIN000003978
JPRN-UMIN000003978已完成未知

agasaki Investigation of Candesartan Effects -the Comparison Between an Increased Candesartan and the additional Diuretics- - NICE-C

Department of Cardiovascular Medicine, Nagasaki University Graduate School of Biomedical Sciences0 个研究点目标入组 100 人开始时间: 2010年8月7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
100

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
40years-old 至 ot applicable(—)
性别
All

入选标准

  • 未提供

排除标准

  • Exclusion criteria comprised any of the following: (1)Patients under treatments with antihypertensive agents except diuretics who will not continue to take 8mg/day of candesartan for at least 3 months. (2)Administration of diuretics or of agents influencing rennin-angiotensin-aldosterone system except for candesartan. (3)Concomitant medications which are expected to be frequently changed. (4)Under treatment of insulin for diabetes. (5)Severe renal dysfunction (eGFR<30 mL/min/1.73m2) (6)Heart failure (NYHA classification III or IV) (7)Malignant hypertension and secondary hypertension. (8)Myocardial infarction, stroke, and revascularization therapies of coronary arteries and/or peripheral arteries within 6 months prior to the registration of this study. (9)Pregnant female (10)Allergic disorder which is problem in the clinical setting. Hypersensitivity or contraindication to candesartan or hydrochlorothiazide. (11)Patients who are judged by doctors as inappropriate patients for the entries of this study

研究者

发起方
Department of Cardiovascular Medicine, Nagasaki University Graduate School of Biomedical Sciences

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