国家神经系统疾病临床医学研究中心数据管理与共享系统

Data Management And Sharing System of China National Clinical Research Center for Neurological Diseases

China Antihypertensive Trial in Acute Ischemic Stroke II (CATIS-2): rationale and design

第一作者:刘丽萍

通讯作者:王拥军,Jiang He

ischemic stroke hypertension randomized clinical trial

基本信息

  • 负责人:刘丽萍
  • 数据来源: CATIS-2
  • 论文编号:OTHERS20210055
  • 发表时间:2021-03-16

2021-03-16

已发表文章

发表杂志:Stroke and Vascular Neurology

发表类型: Protocol

影响因子(IF): 4.081

PMID: 33727409 Pubmed原文链接 全文下载

主要研究背景及目的

Increased blood pressure (BP) for patients who had an acute ischaemic stroke is associated with poor functional outcome, however the optimal timing of antihypertensive therapy is unknown.We aim to compare early antihypertensive treatment to delayed antihypertensive treatment for reducing the risk of composite major disability and mortality at 3 months in acute ischaemic stroke.

方法

The China Antihypertensive Trial in Acute Ischemic Stroke II (CATIS-2) trial is a multicentre, randomised, open- label, blinded-endpoints trial that will be conducted in 100 hospitals in China. The primary outcome is the composite of death and major disability (modified Rankin Scale score ≥3) at 3 months of randomisation.

结论

The CATIS-2 trial will be testing the hypotheses that early BP lowering leads to improved functional outcome without any other harms, and developing clinical guidelines of the BP management for patients who had an acute ischaemic stroke.

主要结果

Antihypertensive treatment will be received immediately after randomisation in the early treatment group, aimed at average systolic BP by 10%–20% reduction within the first 24 hours, and achieving an average BP level of <140/90 mmHg within 5 days. Patients in the delayed treatment group will discontinue any antihypertension medications for the first 7 days of randomisation, and will receive antihypertensive therapy achieving a BP goal of <140/90 mmHg after 7 days.