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临床试验/NCT05995561
NCT05995561已完成不适用

Heidelberg Registry of Atrial Fibrillation

University Hospital Heidelberg1 个研究点 分布在 1 个国家目标入组 12,297 人开始时间: 2009年6月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
12,297
试验地点
1
主要终点
all-cause mortality

研究概览

简要总结

The single-center HERA AFIb registry was created to assess real-world prevalence, demographic characteristics and management of patients with atrial fibrillation (AF) in the era of novel oral anticoagulant regimes (NOAC) presenting in the emergency department (ED) of University of Heidelberg

详细描述

HERA AFIb is a single-center retrospective registry which enrolled consecutive cases presenting with atrial fibrillation at the emergency department of University Hospital of Heidelberg. Clinical parameters and characteristics for cases were assessed retrospectively. Follow-up was performed via review of medical reports, phone calls and postal queries. Outcome parameters included rates for all-cause mortality, non-hemorrhagic stroke, myocardial infarction and major bleeding.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Retrospective

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

  • documented atrial fibrillation
  • availability of at least one hsTnT measurement

排除标准

  • lost to follow-up

结局指标

主要结局

all-cause mortality

时间窗: 24 months

all-cause mortality during follow-up

次要结局

  • major bleeding(24 months)
  • ischaemic stroke(24 months)
  • myocardial infarction(24 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Mustafa Yildirim

Principle investigator

University Hospital Heidelberg

研究点 (1)

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