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临床试验/EUCTR2006-003622-29-DE
EUCTR2006-003622-29-DE进行中(未招募)1 期

The ARRIVE Study (Aspirin to Reduce Risk of Initial Vascular Events) - A Randomized, Double-Blind, Placebo Controlled, Multicenter, Parallel Group Study to Assess the Efficacy (Reduction of Cardiovascular Disease Events) and Safety of 100 mg Enteric-Coated Acetylsalicylic Acid in Patients at Moderate Risk of Cardiovascular Disease - ARRIVE

Bayer AG0 个研究点目标入组 12,000 人开始时间: 2007年8月14日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Bayer AG
入组人数
12,000

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • - elevated total cholesterol
  • - low HDL cholesterol
  • - elevated blood pressure
  • - family history of early CHD
  • - on antihypertensive therapie
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range

排除标准

  • - type I and type II diabetes
  • - prior history of a CVD events (clinical or diagnostic)
  • - standard exclusion criterias for ASA (see protocol)
  • - any condition likely to cause death within 5 years
  • - chronic, frequent use of NSAID´s or COX-2 inhibitors

研究者

发起方
Bayer AG

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The ARRIVE Study (Aspirin to Reduce Risk of Initial... | 临床试验