Multimodal Phenotyping In Patients Referred With Acute Cardiac faiLurE

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Heart Center Freiburg - Bad Krozingen

About this trial

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

Eligibility criteria

Qualifiers

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

Disqualifiers

Not capable of providing informed consent due to reasons not attributable to cardiogenic shock

Cardiogenic shock following cardiothoracic surgery

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

600 Participants
are grouped into 1 trial group