Pupillometry to predict patient-relevant outcomes in patients with acute heart failure
- Conditions
- I50.9Heart failure, unspecified
- Registration Number
- DRKS00027885
- Lead Sponsor
- Immanuel Klinikum Bernau Herzzentrum Brandenburg Universitätsklinikum der MHB
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- All
- Target Recruitment
- 155
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.
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.
Study & Design
- Study Type
- observational
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method