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NCT07643610Recruiting

BEAT-SHOCK Registry

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

Source: ClinicalTrials.gov · Last updated 11 Jun 2026

Brief summary (registry, in English)

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.

Status (registry)
Recruiting
Study type
Observational
Enrollment
8000 (estimated)
First submitted
29 May 2026
Start date
1 Oct 2025
Primary completion date
1 Oct 2035
Lead sponsor
University Hospital, Basel, Switzerland
NCT number
NCT07643610

What you commit to

  • Study type: Observational
  • Planned participants: 8000
  • From 1 Oct 2025 to the primary completion date, 1 Oct 2035
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Age

  • Age \<18 years

Other

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

Criteria the registry did not label

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
University Hospital Basel
Coordinator of this site? Confirm its status
BaselSwitzerlandRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.