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临床试验/JPRN-UMIN000001238
JPRN-UMIN000001238未知4 期

A comparison of a combination drug of an angiotensin II receptor antagonist and a low-dose diuretic vs combination therapy with an angiotensin II receptor antagonist and a calcium channel blocker in hypertensive patients with metabolic syndrome - CATCH (Combination of Antihypertensive Treatment in Chiba)

Hypertension in Metabolic syndrome CHIBA (HMS-CHIBA) Study group0 个研究点目标入组 200 人开始时间: 2008年7月10日最近更新:
适应症

试验速览

阶段
4 期
发起方
入组人数
200

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
Male

入选标准

  • 未提供

排除标准

  • 1) Patients with uncontrolled hypertension (diastolic blood pressure ≥ 110mmHg) 2) Patients with malignant hypertension 3) Patients with uncontrolled diabetes (HbA1c ≥8.0%) 4) Patients with uncontrolled hypertriglyceridemia (TG ≥400mg/dL) 5) Patients who have stroke, AMI and/or critical vascular complications that required hospitalization within 6 months prior to the intervention 6) Patients with liver dysfunction [GPT(ALT) over three times the normal value] 7) Patients with renal failure (serum creatinine ≥2.0 mg/dL) 8) Patients with a previous history of gout attack or uncontrolled hyperuricemia (≥8.0mg/dL) 9) Patients under treatment with insulin 10) Pregnant or breast feeding female patients, including one trying to conceive pregnancy during the planned study period 11) Patients with uncontrolled arhythmia 12) Patients with severe valvular disease including mitral stenosis and incompetence of aortic valve 13) Patients with cardiac insufficiency (NYHA grade III or IV) 14) Patients with a history of hypersensitivity to ingredients of losartan potassium 15) Patients with a history of hypersensitivity to thiazide or thiazide-like diuretics 16) Patients with a history of hypersensitivity to ingredients of dihydropyridines 17) Patients who are considered not eligible for the study by the attending doctor due to medical reasons

研究者

发起方
Hypertension in Metabolic syndrome CHIBA (HMS-CHIBA) Study group

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