A Double Blind, 2:1 Randomised Monocentre Study to Investigate the Efficacy and Safety of Telmisartan (80 mg qd) Concerning the Amelioration of Structural Alterations and Function of Endothelium in Cardiovascular Risk Patients (SAFE-CRP: Structural Alterations and Function of Endothelium in Cardiovascular Risk Patients)
试验速览
- 阶段
- 4 期
- 状态
- 终止
- 入组人数
- 22
- 试验地点
- 4
- 主要终点
- Change of intima/media ratio in the femoral artery measured by intravascular ultrasound (IVUS)
研究概览
简要总结
The aim of this trial is to evaluate the efficacy and safety of telmisartan 80 mg administered once daily in patients with documented coronary artery disease (CAD) and a probably cardiovascular risk profile concerning the amelioration of structural alterations and endothelial function.
The primary objective of this trial is to evaluate the efficacy in particular with regard to the percentage change of atheroma volume in the femoral artery.The secondary objective is to evaluate the change in the plaque size- assessed by intravascular ultrasound, the increase in Flow Dependent Dilation provoked by intraarterial infusion of three increasing concentrations of Acetylcholine, and the change in seated systolic blood pressure.
Endothelial dysfunction is a primary event in atherogenesis and all known cardiovascular risk factors have been associated with endothelial dysfunction before atherosclerotic vascular disease manifests itself clinically. Pivotal to endothelial dysfunction is a disturbance in the function of endothelium-derived nitric oxide (NO). Recently, it could be shown that acute and chronic angiotensin-1 receptor antagonism reversed endothelial dysfunction in atherosclerosis. In experimental atherosclerosis, AT1 receptor blockade appears to have protective effects. Respective potential mechanisms include the prevention of endothelial injury, the augmentation of NO activity, the inhibition of lipid peroxidation and an antiproliferative effect. These findings together with the most recent data that losartan improves endothelial function and NO activity suggest that AT1 receptor antagonism may also be antiatherogenic in patients with atherosclerosis. Angiotensin II influences smooth muscle cell migration, hyperplasia, and hypertrophy. Angiotensin II also enhances production of local superoxide anion, which will inactivate nitric oxide. Inhibition of these reactions by the AT1-Blocker telmisartan may therefore interfere with atherosclerotic plaque formation.
详细描述
Methodology:
2:1 randomised, double-blind and placebo-controlled parallel-group design
Planned/actual number of subjects:
Enrolled: 30/33, randomised: 30/22, completed: 30/15
Duration of treatment:
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
- Double
入排标准
- 年龄范围
- 36 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •> 35 years of age
- •History of coronary artery disease (CAD)
- •Ability to provide written informed consent
排除标准
- •Pre-menopausal women (last menstruation < 1 year prior to start of the screening visit) who:
- •are not surgically sterile; and/or
- •are nursing
- •are of child-bearing potential and are NOT practising acceptable means of birth control, do NOT plan to continue using this method throughout the study and do NOT agree to submit to periodic pregnancy testing during participation in studies of > 3-months duration. Acceptable methods of birth control include oral, implantable or injectable contraceptives
- •Diastolic blood pressure > 110 mmHg or systolic blood pressure > 180 mmHg at any visit during the study (run-in or randomised period)
- •Hepatic and/or renal dysfunction as defined by the following laboratory parameters:
- •SGPT(ALT) or SGOT(AST) > than 2 times the upper limit of normal range
- •Serum creatinine > 2.3 mg/dL
- •Bilateral renal artery stenosis, renal artery stenosis in a solitary kidney, patients post-renal transplant or with only one kidney
- •Clinically relevant hypokalaemia or hyperkalaemia
- •Uncorrected volume depletion
- •Uncorrected sodium depletion
- •Primary aldosteronism
- •Hereditary fructose intolerance
- •Biliary obstructive disorders
- •Patients who have previously experienced symptoms characteristic of angioedema during treatment with ACE inhibitors or angiotensin II receptor antagonists
- •History of drug or alcohol dependency within 6 months
- •Chronic administration of any medications known to affect blood pressure, except medication allowed by the protocol
- •Any investigational therapy within one month of signing the informed consent form
- •Known hypersensitivity to any component of the formulation
- •Any other clinical condition which, in the opinion of the principal investigator, would not allow safe completion of the protocol and safe administration of telmisartan
- •Stroke within the last 6 months
- •Myocardial infarction within the last 30 days
- •Cardiac surgery within the last 3 months
- •Hyperthyroidosis
- •Hemodynamically relevant valvular disease
- •Restrictive hypertrophic cardiomyopathy
- •Unstable angina pectoris
- •CAD with the indication of bypass surgery.
结局指标
主要结局
Change of intima/media ratio in the femoral artery measured by intravascular ultrasound (IVUS)
时间窗: after 39 weeks
次要结局
- Change in plaque size in the femoral artery measured by IVUS(after 39 weeks)
- Increase in FDD (Flow dependent dilation) stimulated by intra-arterial infusion of Acetylcholine (ACH)(after 39 weeks)
- Change in serum inflammatory markers (CRP, MCP-1, oxLDL antibodies, and VCAM)(after 39 weeks)
- Change in seated blood pressure (BP) at trough(after 39 weeks)