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Clinical Trial Summary

The study aims to investigate clinically and prognostically relevant parameters in patients with cardiogenic shock within a monocentric observational clinical register.


Clinical Trial Description

All consecutive patients with a confirmed cardiogenic shock presenting at the internal intensive care Unit (ICU) at the University of Mannheim are included in the register and followed up during ICU stay and after that. Data of patients' admission status, cause of cardiogenic shock, baseline parameters and comorbidities are collected. Extensive information about echocardiography, electrocardiography and imaging procedures are included in the register. Laboratory values, microbiological investigations, organ dysfunction and organ replacement therapies, medication, adverse events, and complications were recorded for several days during the ICU stay (days 1, 2, 3, 5, 7, and 8). Standard scores for critically ill patients were calculated for the day of admission at the ICU if available, and several time points during the ICU stay. The register includes information about the mortality during ICU stay, 30-day mortality, 6-month mortality and 1-year mortality. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05575856
Study type Observational [Patient Registry]
Source Universitätsmedizin Mannheim
Contact Michael Behnes, PhD
Phone 0049621-3836239
Email michael.behnes@umm.de
Status Recruiting
Phase
Start date June 1, 2019
Completion date December 1, 2023

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