BEAT-SHOCK Registry

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity Hospital, Basel, Switzerland

About this trial

This regulation defines the purpose, the operational processes, and the organization of the registry BEAT-SHOCK (Basel Evaluation of Acute Therapy in cardiogenic SHOCK). It describes the requirements for collecting, storing, processing, managing and sharing health-related registry data.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients admitted with cardiogenic shock to the University hospital Basel (diagnosis at the time of admission) or development of cardiogenic shock during the hospital stay

Age ≥18 years

Provision of written ICF

Clinical diagnosis of cardiogenic shock.

Disqualifiers

Age <18 years

Refusal to provide informed consent by the patient or their legally authorized representative

Trial population

Adult patients who are treated at the University Hospital Basel and are diagnosed with cardiogenic shock, irrespective of underlying etiology or therapeutic strategy. The registry includes a wide range of cardiogenic shock etiologies, including: * Myocardial infarction (MI) * Fulminant myocarditis * Acute decompensated heart failure * Severe valvular disease * Post-cardiotomy or perioperative cardiogenic shock

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • no internvention

    Other intervention

    This is a health data registry.

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

In-Hospital all-cause mortality occurring before discharge from the participating study centre

In-hospital all-cause mortality is defined as death occurring before discharge from the participating study centre. Deaths occurring after transfer to an external hospital are not counted as in-hospital deaths, but are captured through follow-up for 30-day and 90-day mortality.

Time frame
10 years

Secondary outcomes

1

30-day and 90-day all-cause Mortality

30-day and 90-day all-cause mortality occuring after discharge from the participating study centre.

Time frame
30, 90 days
2

Need for organ support at any time during hospitalization

The need for organ support at any time during hospitalization (including renal replacement therapy, mechanical circulation support irrespective of type, and vasoactive or inotropic therapy)

Time frame
30, 60, 360 days
3

Acute kidney injury (AKI) within 36 hours after index diagnosis of cardiogenic shock/index presentation

Occurence of AKI (defined as an increase in serum creatinine of at least 26 µmol/L (0.3 mg/dL)

Time frame
Within 36 hours after index diagnosis of cardiogenic shock/ index presentation.

Other outcomes

Sponsors and contacts

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