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临床试验/NCT06411340
NCT06411340
尚未招募
不适用

An Observational-based Registry of Routinely Collected Clinical Parameters to Study Inflammation in Acute Cardiovascular Diseases - the CArdiovascular Inflammation Registry

King's College London0 个研究点目标入组 1,000 人2024年7月

概览

阶段
不适用
干预措施
未指定
疾病 / 适应症
Inflammation
发起方
King's College London
入组人数
1000
主要终点
All-cause mortality
状态
尚未招募
最后更新
去年

概览

简要总结

Following acute cardiovascular injury, inflammation is vital to activate reparative mechanisms. However, there is compelling evidence implicating excessive inflammation and dysregulated resolution in fibrosis, ventricular remodelling, and heart failure (HF). Recently, the anti-inflammatory agent colchicine reduced cardiovascular events after myocardial infarction (MI) compared to placebo, indicating that targeting inflammation in acute cardiovascular conditions is feasible. Several acute cardiovascular conditions are characterised by inflammation, including myocarditis, MI, and acute heart failure. However, there is large variability in definition, epidemiology, clinical presentation, pathophysiology, and natural history of acute inflammatory cardiovascular diseases. This relates, in part, to the difficulty in performing adequately powered studies. Clinical studies that include sufficient patients and extended observation periods are necessary to address some of these knowledge gaps. This registry aims to collate routinely collected clinical data on patients with acute cardiovascular diseases characterised by inflammation in an observational-based registry. By doing so, the investigators hope to understand the contribution of inflammation to the pathophysiology of acute cardiovascular disease, improve risk stratification, and identify potential novel therapeutic targets.

注册库
clinicaltrials.gov
开始日期
2024年7月
结束日期
2039年7月
最后更新
去年
研究类型
Observational
性别
All

研究者

责任方
Sponsor

入排标准

入选标准

  • Any patient 13 years of age or older with an acute cardiovascular condition requiring hospital admission is eligible.

排除标准

  • \<13 years of age

结局指标

主要结局

All-cause mortality

时间窗: 1 year

Primary outcome will include all-cause mortality, but will vary by specific research project conducted within the registry.

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