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Registry of Adults Treated for Cardiogenic Shock at a Basel Hospital

Collects health data on adults with cardiogenic shock, a sudden severe heart failure.

Plain-language title generated from the registry record
Registry title: BEAT-SHOCK Registry

Key facts

Where
Basel, SwitzerlandSee the site

Where in Switzerland

  • University Hospital BaselBasel, SwitzerlandTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
University Hospital, Basel, Switzerland
Trial code
NCT07643610
Record updated
11 June 2026
Original description
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.Read full original descriptionShow less

BEAT-SHOCK (Basel Evaluation of Acute Therapy in Cardiogenic SHOCK) Registry

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.

Exclusion: Age <18 years; Refusal to provide informed consent by the patient or their legally authorized representative.

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; impaired organ perfusion due to primary cardiac dysfunction,; persistent systolic blood pressure (SBP) <90 mmHg for ≥30 minutes, or the need for vasopressors, inotropes, or mechanical circulatory support (MCS) to maintain adequate perfusion and; evidence of systemic hypoperfusion with arterial lactate ≥2 mmol/L or venous lactate ≥3 mmol/l and ≥1 of the following:; Cold or clammy extremities; Altered mental status; Reduced urine output; Signs of volume overload or congestion (on clinical exam, imaging, or invasive monitoring); Patients with normotensive cardiogenic shock (SBP ≥90 mmHg without vasopressors or MCS) may also be included if clear signs of hypoperfusion (arterial lactate ≥2 mmol/L or venous lactate ≥3 mmol/l) and cardiac dysfunction are present and alternative causes are excluded.

ClinicalTrials.gov NCT07643610