Multimodal Phenotyping In Patients Referred With Acute Cardiac faiLurE
Recruiting now
Conditions studied: Cardiogenic Shock, Acute Heart Failure (AHF)
In brief
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
Key facts
- Study ID
- NCT07515508
- Run by
- University Heart Center Freiburg - Bad Krozingen
- People needed
- 600
- Starts
- 2024-08-07
- Expected to finish
- 2028-07-31
- Last updated by the study team
- 2026-07-29
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients hospitalized with acute heart failure SCAI stage B - E.
You may not qualify if…
- Not capable of providing informed consent due to reasons not attributable to cardiogenic shock
- Cardiogenic shock following cardiothoracic surgery
Where it is running
- University Heart Center Freiburg - Bad Krozingen — Bad Krozingen, Germany (enrolling)
- University Medical Center Freiburg, Interdisciplinary Medical Intensive Care — Freiburg im Breisgau, Germany (enrolling)
- Department for Internal Medicine 8, Clinic for Cardiology and Rhythmology, University Clinic of the Paracelsus Medi-cal University Nuremberg — Nuremberg, Germany (enrolling)
- Schwarzwald Baar Klinikum Villingen-Schwenningen, Klinik für Kardiologie und Intensivmedizin — Villingen-Schwenningen, Germany (enrolling)
Full record on ClinicalTrials.gov
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