跳至主要内容
临床试验/DRKS00027885
DRKS00027885尚未招募不适用

Pupillometry to predict patient-relevant outcomes in patients with acute heart failure - PURE

Immanuel Klinikum Bernau Herzzentrum Brandenburg Universitätsklinikum der MHB0 个研究点目标入组 155 人开始时间: 2023年1月30日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
155

研究概览

简要总结

暂无简介。

研究设计

研究类型
Observational

入排标准

年龄范围
18 Years 至 one(—)
性别
All

入选标准

  • Target group:
  • Adult inpatients of the cardiology department of the Heart Centre Brandenburg, Immanuel Klinikum Bernau with acute de novo heart failure or acute decompensation of chronic heart failure (acute decompensated chronic heart failure) and a written informed consent to participate in the study.
  • Control group:
  • A parallel group of adults, matched for age and sex, without acute de novo heart failure or acute decompensated chronic heart failure, with written informed consent to participate in the study.

排除标准

  • Individuals with a history of eye surgery or diseases that may affect pupillary function (e.g. severe retinopathy), patients who are unable to follow the representations on the computer screen during the eye tracking study due to poor visual acuity, and patients who are unable to understand the scope and content of the study to provide written informed consent to participate in the study will be excluded from the study.

研究者

发起方
Immanuel Klinikum Bernau Herzzentrum Brandenburg Universitätsklinikum der MHB

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