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临床试验/NCT00634712
NCT00634712已完成3 期

Candesartan Cilexetil in Heart Failure Assessment of Reduction in Mortality and Morbidity. Clinical Study of Candesartan in Patients With Heart Failure and Preserved Left Ventricular Systolic Function

AstraZeneca0 个研究点目标入组 734 人开始时间: 1999年6月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
AstraZeneca
入组人数
734
主要终点
Cardiovascular mortality or hospitalisation due to congestive heart failure

研究概览

简要总结

A study to evaluate the effect of Atacand on patients with heart failure with preserved left ventricular function

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Male or female aged 18 or above
  • Congestive Heart Failure with symptoms for more than 4 weeks before starting study
  • Provision of informed consent

排除标准

  • Current low blood pressure with symptoms
  • Liver disease considered significant by the study doctor
  • Pregnant or lactating females

研究组 & 干预措施

1

Active Comparator

干预措施: Candesartan (Drug)

2

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Cardiovascular mortality or hospitalisation due to congestive heart failure

时间窗: , 4, 6 weeks, 6 months, every 4 months thereafter until 24 months

次要结局

  • Cardiovascular mortality or hospitalisation for management of congestive heart failure, or non fatal MI(Cardiovascular mortality or hospitalisation for management of congestive heart failure, or non fatal MI)

研究者

发起方
AstraZeneca
申办方类型
Industry

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