跳至主要内容
临床试验/NCT07515508
NCT07515508招募中不适用

Multimodal Phenotyping In Patients Referred With Acute Cardiac faiLurE

University Heart Center Freiburg - Bad Krozingen5 个研究点 分布在 1 个国家目标入组 600 人开始时间: 2024年8月7日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
600
试验地点
5
主要终点
Mortality

研究概览

简要总结

The goal of this observational study is to learn whether information collected during routine hospital care, together with blood and urine samples, can help doctors better identify different types of cardiogenic shock and better predict outcomes in adults hospitalized with acute heart failure and cardiogenic shock. The main question is whether clinical findings, imaging results, and biomarkers, including sex-specific factors, are associated with the risk of death within 30 days. Participants will not receive an experimental treatment. Researchers will collect data from routine care, collect additional blood and urine samples for biobanking, and follow participants after hospital discharge

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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

  • Patients hospitalized with acute heart failure SCAI stage B - E.

排除标准

  • Not capable of providing informed consent due to reasons not attributable to cardiogenic shock
  • Cardiogenic shock following cardiothoracic surgery

研究组 & 干预措施

Arm 1

结局指标

主要结局

Mortality

时间窗: 30 days

次要结局

  • Rehospitalization for heart failure(From hospital discharge until 12 months)
  • Rehospitalization for cardiac reasons (non-elective)(From hospital discharge until 12 months)
  • Mortality(6 and 12 months)

研究者

发起方
University Heart Center Freiburg - Bad Krozingen
申办方类型
Other
责任方
Sponsor

研究点 (5)

Loading locations...

相似试验

Multimodal Phenotyping In Patients Referred With... | 临床试验