跳至主要内容
临床试验/NCT03313687
NCT03313687招募中不适用

SafeTy and Outcome of contemPorary Treatment Strategies for Cardiogenic SHOCK - an International, Observational Registry

Universitätsklinikum Hamburg-Eppendorf1 个研究点 分布在 1 个国家目标入组 2,500 人开始时间: 2017年9月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
入组人数
2,500
试验地点
1
主要终点
All-cause mortality

研究概览

简要总结

International, observational registry to investigate the outcome in patients with cardiogenic shock. The primary aim of this study is to investigate the clinical outcome of patients in cardiogenic shock.

详细描述

There is a focus on interventional therapies, mechanical circulatory support and new cardiovascular therapeutics in patients with cardiogenic shock (CS). The investigators will describe current practice in study sites including concomitant patients with CS. Therefore, the investigators will monitor drug therapies initiated, devices being utilized as well as outcome and side effect of possible interventions

研究设计

研究类型
Observational
观察模型
Cohort
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

  • Patients with cardiogenic shock treated at a tertiary care hospital.

排除标准

  • Age ≤17 years.

结局指标

主要结局

All-cause mortality

时间窗: Within 30 days after admission.

by registration office

次要结局

  • Ischemic events, bleeding events, heart failure, sepsis, dialysis.(Within 12 months after admission.)
  • All-cause mortality(Within 12 months after admission.)

研究者

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

PD Dr. Dirk Westermann

Professor

Universitätsklinikum Hamburg-Eppendorf

研究点 (1)

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