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临床试验/NCT00225849
NCT00225849Unknown4 期

Japanese Primary Prevention Project With Aspirin in the Elderly With One or More Risk Factors of Vascular Events: JPPP

Ministry of Health, Labour and Welfare, Japan2 个研究点 分布在 1 个国家目标入组 10,000 人开始时间: 2005年3月1日最近更新:
适应症
相关药物

试验速览

阶段
4 期
发起方
入组人数
10,000
试验地点
2
主要终点
Composite event of cerebro/cardiovascular (CV) death, nonfatal cerebral stroke (of any cause) and nonfatal myocardial infarction (MI)

研究概览

简要总结

The purpose of this study is to investigate the balance between the risks and benefits of primary prevention by Aspirin in elderly Japanese patients with one or more cerebro/cardiovascular risk factors

详细描述

Cerebro/cardiovascular (CV) death accounts for approximately 30% of total deaths in Japan and therefore it is important to establish a preventive treatment for CV events from the point of public health. The guidelines proposed by a joint study group centering on the Japanese Circulation Society, recommend administration of aspirin to patients with multiple risk factors for primary prevention of arteriosclerotic diseases. In addition, the 2002 AHA guidelines recommend use of aspirin in patients with a 10% or higher 10-year risk of CV events. However, these descriptions are founded on randomized, comparative study results and epidemiological data obtained outside Japan, while no epidemiological data are available in Japan that would allow prediction and selection of patients who could benefit from primary prevention with aspirin. Although the benefit of aspirin for secondary prevention has been proven in Japanese patients, the benefits of primary prevention are still controversial.

JPPP is a multicenter, open-label, centrally randomized, controlled trial. In total, 10,000 elderly patients with one or more CV risk factors (age 60-85 years combined with hypertension, hyperlipidemia, and/or diabetes) will be assigned to enteric-coated aspirin (100mg/day) or control. The primary endpoint is composite event of CV death, nonfatal stroke (of any cause) and nonfatal myocardial infarction.

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
None

入排标准

年龄范围
60 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Elderly patients not previously diagnosed to have any arteriosclerotic disease, including coronary artery disease or cerebrovascular disease, but meeting any one or more of the following criteria (or on medication for any one or more of the following conditions).
  • Hypertension: SBP ≥ 140 mmHg or DBP ≥ 90 mmHg
  • Hyperlipidemia: Hypercholesterolemia (total cholesterol ≥ 220 mg/dL or LDL cholesterol ≥ 140 mg/dL) or Hypertriglyceridemia (Triglycerides ≥ 150 mg/dL) or Low-HDL cholesterolemia (HDL cholesterol < 40 mg/dL)
  • Diabetes: Fasting morning blood glucose ≥ 126 mg/dL or casual blood glucose ≥ 200 mg/dL or blood glucose at 2 hrs in the 75-g glucose tolerance test ≥ 200 mg/dL, or HbA1c ≥ 6.5%
  • Age: 60 to 85 years
  • Patients who can give written consent for participation in the study

排除标准

  • Patients with a history of coronary artery disease or cerebrovascular disease (including transient ischemic attack)
  • Patients with arteriosclerotic disease requiring surgery or intervention
  • Patients who have or may have atrial fibrillation
  • Patients being treated with aspirin, other antiplatelet agents or anticoagulants
  • Patients using NSAIDs chronically
  • Patients with a history of hypersensitivity to aspirin or salicylic acid
  • Patients with peptic ulcers
  • Patients with a bleeding tendency
  • Patients with serious blood abnormalities
  • Patients with aspirin-sensitive asthma or a history of the same
  • Patients who are otherwise judged by the investigator to be unsuitable for enrollment in the study.

结局指标

主要结局

Composite event of cerebro/cardiovascular (CV) death, nonfatal cerebral stroke (of any cause) and nonfatal myocardial infarction (MI)

次要结局

  • CV death
  • Non CV death
  • Nonfatal cerebral stroke
  • Nonfatal MI
  • Angina pectoris
  • Transient ischemic attack
  • Arteriosclerotic disease requiring surgery or intervention
  • Extracranial bleeding requiring transfusion or admission
  • Severe side-effects that lead to interruption of the study medication.

研究者

发起方
Ministry of Health, Labour and Welfare, Japan
申办方类型
Other Gov

研究点 (2)

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