Shock and Acute Conditions OutcOmes Platform
NCT06376318 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000
Last updated 2024-04-19
Summary
In-hospital mortality of patients admitted in the intensive care unit (ICU) for circulatory shock remains high (between 20 and 40%).
Currently, there are no markers that allow us to classify patients with circulatory shock at higher risk of early and late bad outcomes, or who may better respond to a specific intervention.
To understand the contribution of biological heterogeneity to circulatory shock independently from its etiology, the ShockCO-OP Research Program aims to use clustering approaches to re-analyze existing clinical and molecular data from several large European and North American prospective cohorts and clinical trials.
This will enable an improvement in risk prediction and a better patient selection in future clinical trials to assess a personalized therapy (i.e., prospective enrollment based on a biological/molecular signature).
Conditions
- Circulatory Shock
- Sepsis
- Cardiogenic Shock
- Major Trauma
- Surgical Shock
Interventions
- DRUG
-
Inotrope
Vasopressors: Norepinephrine, vasopressin Inotropes: Epinephrine, Dobutamine, Milrinone
- DEVICE
-
Mechanical circulatory support
Intra-aortic balloon pump Extracorporeal membrane oxygenation (ECMO)
- DRUG
-
anti-bodies
Anti-Dipeptidyl peptidase 3 (DPP3), Anti-Bioactive adrenomedullin (bio-ADM)
Sponsors & Collaborators
-
University of Helsinki
collaborator OTHER -
University of Ottawa
collaborator OTHER -
University of Leipzig
collaborator OTHER -
University of Nancy
collaborator OTHER - collaborator OTHER
- collaborator OTHER
-
University of Paris 5 - Rene Descartes
collaborator OTHER -
University of Toronto
collaborator OTHER -
Saint-Louis Hospital, Paris, France
lead OTHER
Principal Investigators
-
Claudia dos Santos, MD, PhD · Unity Health Toronto
-
Alexandre Mebazaa, MD, PhD · St Louis and Lariboisiere Hospitals
Eligibility
- Min Age
- 18 Years
- Max Age
- 90 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2024-01-01
- Primary Completion
- 2025-07-01
- Completion
- 2026-01-01
Countries
- Canada
Study Locations
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