Clinical trial Recruiting at 1 site Observational Ages 18 and up

BEAT-SHOCK: Baseline Registry for Acute Cardiogenic Shock at Basel

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

Run by University Hospital, Basel, Switzerland · NCT07643610 · Data updated 2026-11-12

This registry collects and shares data on adults with cardiogenic shock admitted to University Hospital Basel to help understand how these patients are treated and how they fare.

Quick facts

Study typeObservational
Ages18 Years and up
SexAll
Enrollment8000 (estimated)
SponsorUniversity Hospital, Basel, Switzerland
Academic / other
Locations1 site (Basel, Canton of Basel-City)
StatusRecruiting
StartedOctober 1, 2025
Main results expectedOctober 1, 2035
Study endsOctober 1, 2035
Registry record updatedJune 11, 2026
Trial IDNCT07643610 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults (18 years or older) with clinical cardiogenic shock admitted to University Hospital Basel or who develop shock during their stay, who provide informed consent.

Probably not a fit

Patients without cardiogenic shock or those who do not meet consent requirements may not benefit from registry insights.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

BEAT-SHOCK is an observational registry that documents patients with cardiogenic shock admitted to or developing during hospitalization at University Hospital Basel. The registry focuses on how acute cardiac failure and related conditions are managed, and how data are collected, stored, processed, and shared. It does not involve an experimental treatment, and there are no interventions being tested within the registry. Participation requires informed consent and adherence to data handling requirements. Findings from the registry may inform future clinical practice and research in cardiogenic shock and related conditions.

Why it matters

Potential benefit: If successful, the registry could improve understanding of cardiogenic shock patterns and treatment outcomes to guide future care.

How similar studies have gone: Other registries have contributed valuable insights into cardiogenic shock management, though this exact Basel registry provides local context.

Who can join: the full rules

Show full inclusion / exclusion criteria
* 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

Exclusion criteria:

* Age \<18 years
* Refusal to provide informed consent by the patient or their legally authorized representative

Where it's running

  • University Hospital Basel
    Basel, Canton of Basel-City, Switzerland
    Recruiting

Study contacts

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.