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临床试验/NCT00794885
NCT00794885已完成4 期

Enalapril Maleate and Folic Acid Tablets for Primary Prevention of Stroke in Patients With Hypertension: a Post-marketing, Double-blind, Randomized Controlled Trial.

Shenzhen Ausa Pharmed Co.,Ltd2 个研究点 分布在 1 个国家目标入组 20,702 人开始时间: 2008年5月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
4 期
状态
已完成
发起方
入组人数
20,702
试验地点
2
主要终点
First attack of symptomatic stroke ( ischemic or hemorrhagic)

研究概览

简要总结

The purpose of this trial is to confirm that enalapril maleate and folic acid tablets is more effective in preventing stroke among the patients with primary hypertension when compared to enalapril maleate.

详细描述

Primary hypertension is the most important risk factor leading to cardiovascular events. Successful management of hypertension is a key to prevent these events. Hyperhomocysteinemia (HHcy) is another independent risk factor, especially for stroke. Our team's prospective nested case-control study of 39165 subjects in China showed that incidence of cardiovascular events (especially stroke) was strongly associated with plasma level of total homocysteine (tHcy). The coexistence of hypertension and HHcy dramatically increased the risk of stroke by 25 to 30 times as compared to the subjects without the two risk factors (Graham et al, 1997). Findings from previous and our studies clearly indicate that simultaneous control of hypertension and HHcy is pivotal in reducing cardiovascular events morbidity and mortality in China.

It has been well documented that folic acid is effective in lowering the level of plasma tHcy. While controversial remains on its efficacy on preventing cardiovascular events, a study done by our team: "Efficacy of folic acid supplementation in stroke prevention: a meta-analysis" (Wang et al, 2007) provide coherent evidence that folic acid supplementation can decrease the risk of stroke by 18%, and 25% in populations where folic fortification was not issued, or used for primary prevention.

C677T gene polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) is one of the genetic determinators of plasma tHcy level. Observational studies showed that individuals with TT genotype tend to have high plasma tHcy and elevated risk of cardiovascular events (Cronin et al. 2005), and folic acid supplementation led to a remarkable reduction in plasma tHcy. In short, previous studies by others and by our team have provided strong rationale for our proposed trial as detailed below.

The hypothesis of the current study is that a combination of antihypertensive drug (e.g., enalapril) with folic acid is not only efficacious, but also is safe and highly cost-effective than antihypertensive (e.g., enalapril) used alone to prevent stroke in hypertensive patients.

This trial will enroll 20,000 patients with primary hypertension and with known MTHFR C677T genotype. Subjects will be first stratified by genotypes, and then randomly assigned to treatment groups. The study patients will be instructed to take orally enalapril 10 mg daily or enalapril/folic acid 10mg/0.8mg tablets daily for a maximum of 5 years. The follow-up is given every 3 months.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
45 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • BP≥140/90 mmHg in both of the two screening visits or currently under anti-hypertension treatment
  • 45 - 75 years old
  • Successful determination of MTHFR C677T genotype
  • For pre-menopausal women, agreed to use contraceptives during the trial
  • Signed the written informed consent

排除标准

  • Having a history of stroke
  • Having a history of myocardial infarction
  • Having a history of physician diagnosed heart failure
  • Post- coronary revascularization
  • Severe somatic disease such as cancer
  • Secondary hypertension
  • Congenital or acquired organic heart diseases
  • Contraindicated to angiotensin-converting enzyme inhibitor(ACEI)
  • History of ACEI adverse effects
  • Currently long-term use of folic acid or vitamin B12 or vitamin B6
  • Pregnant or child breastfeeding women
  • Severe mental disorders
  • Lab tests indicating abnormal liver or kidney function
  • Unwilling to participate the trial, unwilling to change the current antihypertensive treatment

研究组 & 干预措施

Enalapril/folic acid

Experimental

A fixed combination drug is given. The dose is fixed in enalapril 10 mg / folic acid 0.8 mg per day.

干预措施: Enalapril/folic acid (Drug)

Enalapril

Active Comparator

Enalapril maleate 10 mg per day is given

干预措施: Enalapril maleate (Drug)

结局指标

主要结局

First attack of symptomatic stroke ( ischemic or hemorrhagic)

时间窗: during the trial period

Patients are followed-up every 3 months. All endpoint outcomes are assessed by the Endpoint Adjudication Committee of the study.

次要结局

  • Composite major cardiovascular events(during the trial period)
  • All-cause death(during the trial period)
  • First attack of ischemic stroke and resultant death(during the trial period)
  • First attack of hemorrhagic stroke and resultant death(during the trial period)
  • Myocardial infarction and resultant death(during the trial period)

研究者

发起方
Shenzhen Ausa Pharmed Co.,Ltd
申办方类型
Industry
责任方
Sponsor

研究点 (2)

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