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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00027885
Enrollment
155
Registered
2023-01-30
Start date
2023-02-01
Completion date
Unknown
Last updated
2025-04-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

I50.9

Interventions

Group 1: Heart failure group: pupillometric examinations with a hand-held pupillometer (PLR-3000) and an eye tracker (Eyelink 1000 Plus), cognitive stress (reproducing series of numbers), Determinatio

Sponsors

Immanuel Klinikum Bernau Herzzentrum Brandenburg Universitätsklinikum der MHB
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: 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.

Exclusion criteria

Exclusion criteria: 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.

Design outcomes

Primary

MeasureTime frame
Combined endpoint of cardiac events within 1 year after index hospitalisation (myocardial infarction, stroke, rehospitalisation within 90 days due to de novo /acute decompensated heart failure and cardiovascular mortality)

Secondary

MeasureTime frame
Secondary endpoints are the parameters included in the combined endpoint, 1-year all-cause mortality and incidence of heartburn/stomach ulcer . Other endpoints include changes in pupil size, pupillary light reflex, microsaccade rate and amplitude, and working memory capacity.

Countries

Germany

Contacts

Public ContactAnja Haase-Fielitz

Immanuel Klinikum Bernau Herzzentrum Brandenburg Universitätsklinikum der MHB

anja.haase-fielitz@immanuelalbertinen.de+49 3338 694-649

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026