Polish Nationwide Registry of Diagnostics, Treatment and Outcome in Patients With Cardiogenic Shock

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorWroclaw Medical University

About this trial

The registry objective is to get information on current epidemiology, diagnostics, treatment and outcome in patients with cardiogenic shock in Poland. Obtained information will help to plan the nationwide initiative for modern cardiogenic shock treatment with established place for mechanical circulatory support.

It is hypothesized that the treatment and outcome of cardiogenic shock, including mechanical circulatory support, are currently poor in Poland and should be improved. Unfortunately, without status quo data, efficient planning for its improvement cannot be conducted, hence the CaS-POL registry initiative.

Eligibility criteria

Qualifiers

Cardiogenic shock patients of all etiologies in SCAI stage B, C, D, E.

age > 18 years old

persistent hemodynamic failure defined as systolic blood pressure of <90 mmHg for ≥ 30 minutes or the requirement for inotropic or vasopressor agents with evidence of hypoperfusion of the peripheral organs

Disqualifiers

patients without return of spontaneous circulation who were considered to extracorporeal cardiopulmonary resuscitation (ECPR)

primary septic, anaphylactic, hypovolemic shock

post-operative cardiogenic shock

end-stage of heart failure disqualified from mechanical circulatory support and heart transplantation

Trial design

Treatments tested in this trial

  • Not listed

Trial groups

500 Participants
are grouped into 1 trial group

Sponsors and collaborators

Wroclaw Medical University

Lead sponsor

Polish Cardiac Society

Collaborator

Johnson & Johnson

Collaborator