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临床试验/NCT03626506
NCT03626506Unknown不适用

Evaluation of spironolactoNe Versus Indapamide on Target Organ Damage in Patients With Obesity and hYpertension(ENVOY)

Peking University Third Hospital1 个研究点 分布在 1 个国家目标入组 400 人开始时间: 2019年2月13日最近更新:
适应症
干预措施
相关药物

试验速览

阶段
不适用
入组人数
400
试验地点
1
主要终点
left atrial volume index (LAVI)

研究概览

简要总结

Most recent guidelines continue to recommend thiazide diuretics as first-line agents for patients with hypertension in spite of the potential metabolic side effects, while mineralocorticoid receptor antagonists (MRAs), such as spironolactone or eplerenone, are mainly recommended to be used in patients with resistant hypertension or heart failure.However,animal studies demonstrated that MRAs induce beneficial changes in left ventricular remodeling and prevent or partially reverse cardiac fibrosis and pathological hypertrophy that contribute to the development of diastolic heart failure. MRAs have also been shown to decrease inflammation and myocardial fibrosis in patients with obesity and the metabolic syndrome. In the proposed study, the investigators planned to randomize 400 patients with essential hypertension and increased waist circumference to receive spironolactone or indapamide in combination with amlodipine for 12 months. The effects of the two diuretics on target organ damage detected by changes in left atrial volume index(LAVI) by echocardiography reflecting left ventricular diastolic dysfunction or changes in carotid-femoral pulse wave velocity(PWV) reflecting arterial stiffness will be compared. The potential role of MRAs as initial therapy for patients with essential hypertension and visceral obesity will be evaluated.

详细描述

Thiazide diuretics have been widely used for the management of essential hypertension, especially in patients with salt-sensitive hypertension. Most recent guidelines continue to recommend thiazide diuretics as first-line agents for all patients with hypertension in spite of the potential metabolic side effects such as hypokalemia, hypertriglyceridemia, impaired glucose tolerance and increases in serum cholesterol and uric acid. However, mineralocorticoid receptor antagonists (MRAs), such as spironolactone or eplerenone, are mainly recommended to be used in patients with resistant hypertension or heart failure because they have never been evaluated for efficacy in reducing cardiovascular events in uncomplicated patients with hypertension. Indeed, it has been demonstrated that MRAs reduced total mortality or cardiovascular death in patients with systolic heart failure with severe or mild symptoms and in patients undergoing hemodialysis for chronic renal dysfunction. Animal studies demonstrated that MRAs induce beneficial changes in left ventricular remodeling and prevent or partially reverse cardiac fibrosis and pathological hypertrophy that contribute to the development of diastolic heart failure. MRAs have also been shown to decrease inflammation and myocardial fibrosis in patients with obesity and the metabolic syndrome. Of interest is the recent finding in EMPHASIS-HF study in which almost all of the benefit of eplerenone was found in those patients with an increased waist circumference. Therefore, the investigators have reason to believe that MRAs will be more effective than thiazide diuretics in preventing target organ damage and can be used initially in patients with essential hypertension and visceral obesity. In the proposed study, the investigators planned to randomize 400 patients with essential hypertension and increased waist circumference to receive spironolactone or indapamide in combination with amlodipine for 12 months. The effects of the two diuretics on target organ damage detected by changes in left atrial volume index(LAVI) by echocardiography reflecting left ventricular diastolic dysfunction or changes in carotid-femoral pulse wave velocity(PWV) reflecting arterial stiffness will be compared. If it proves that spironolactone as first-line antihypertensive medication is more effective than indapamide in target organ protection, the investigators would propose a large scale cardiovascular outcome trial to evaluate cardiovascular events in patients with essential hypertension and visceral obesity.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients with essential hypertension aged between 18-80years
  • Office systolic blood pressure (SBP)≥140mmHg and <180mmHg without treatment or on one antihypertensive drug or SBP<140mmHg on two antihypertensive drugs
  • Waist circumference ≥90cm for males, ≥ 80cm for females

排除标准

  • Secondary hypertension.
  • Symptomatic congestive heart failure or history of heart failure.
  • History of ischemic stroke, unstable angina or myocardial infarction;
  • Atrial fibrillation
  • Serum creatinine ≥ 2.0mg/dl or eGFR≤ 30 ml/min/1.73 m2
  • Serum K+ ≥ 5.0 mmol/L or ≤3.5 mmol/L

研究组 & 干预措施

spironolactone

Experimental

Subjects will take spironolactone 20~40mg once daily on top of amlodipine 5~10mg once daily.

干预措施: Spironolactone (Drug)

spironolactone

Experimental

Subjects will take spironolactone 20~40mg once daily on top of amlodipine 5~10mg once daily.

干预措施: Amlodipine (Drug)

indapamide

Active Comparator

Subjects will take indapamide 1.5~3.0mg once daily on top of amlodipine 5~10mg once daily.

干预措施: Indapamide (Drug)

indapamide

Active Comparator

Subjects will take indapamide 1.5~3.0mg once daily on top of amlodipine 5~10mg once daily.

干预措施: Amlodipine (Drug)

结局指标

主要结局

left atrial volume index (LAVI)

时间窗: 12 months

change in left atrial volume index (LAVI) from baseline to the end of study period of 12 months

次要结局

  • carotid-femoral pulse wave velocity (PWV)(12 months)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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