Workpackage 02: Prospective CULPRIT-SHOCK registry
Objectives of the Workpackage
The main objective of workpackage 02 is:
- To set-up a multinational European collaborative network of tertiary care centres for enrolment of patients with AMI and cardiogenic shock qualifying for the registry
- To obtain ethical approval for all participating centres according to the respective laws and rules in all participating countries for registry patients
- To include patients not eligible for randomization (WP01) into the registry
- To describe the reasons for inclusion into the registry and the 30-day outcome of patients with cardiogenic shock after AMI non-eligible for the randomized CULPRIT-SHOCK trial
- To perform intermediate and long-term follow-up at 6 and 12 months to further define the outcome of patients with cardiogenic shock in the registry