Actively Recruiting
Multi-center Collaborative to Enhance Quality and Outcomes in the Management of Cardiogenic Shock
Led by STAVROS G DRAKOS · Updated on 2026-03-20
500
Participants Needed
3
Research Sites
292 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This large real-world international prospective registry will provide a unique opportunity to comprehensively understand the contemporary management, clinical course and short as well as long-term outcomes of all Cardiogenic Shock (CS) patients cared for at four high volume dedicated shock care centers. As the first true North American multicenter CS collaborative with a uniform dedicated and comprehensive case report form, the high patient volumes and wide spectrum of clinical acuity seen at these institutions will provide valuable insight into the factors associated with adverse outcomes; and will serve as a blueprint for future clinical trial designs that may better inform clinical practice.
CONDITIONS
Official Title
Multi-center Collaborative to Enhance Quality and Outcomes in the Management of Cardiogenic Shock
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Primary diagnosis of cardiogenic shock at time of index evaluation; including acute myocardial infarction- and acute decompensated heart failure-cardiogenic shock phenotypes
- Patients with cardiac arrest complicating cardiogenic shock and those with massive pulmonary embolism with right ventricular cardiogenic shock will also be eligible for the registry
You will not qualify if you...
- Patients with shock not due to primary cardiac etiology will be excluded. These include septic, hemorrhagic, and anaphylactic shock.
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Cleveland Clinic Florida
Weston, Florida, United States, 33331
Actively Recruiting
2
Inova Heart and Vascular Institute
Falls Church, Virginia, United States, 22042
Actively Recruiting
3
University of Toronto
Toronto, Ontario, Canada
Actively Recruiting
Research Team
J
John Kirk
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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