Shock and Acute Conditions OutcOmes Platform

NCT06376318 · Status: ACTIVE_NOT_RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2024-04-19

No results posted yet for this study

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
  • McGill University

    collaborator OTHER
  • Mayo Clinic

    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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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06376318 on ClinicalTrials.gov