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Recruiting Observational

Patient Outcome of Cardiac Surgery During the COVID-19 Pandemic

NCT04389463 · tracked via the Priya Life Science France tracker
Phase
Observational
Started
2020-05-11
Last updated
2025-09-08

Condition(s) studied

Patients Undergoing Cardiac or Thoracic Surgery

Investigational drug(s) / intervention(s)

No intervention

No intervention: No description

Study summary

This study will describe the recovery process of patients undergoing cardiac surgery during the covid-19 pandemic. This will focus on hemodynamic failure and organ dysfunction after surgery.

Capturing real-world data and sharing international experience will inform the management of this complex group of patients who undergo surgery throughout the COVID-19 pandemic, improving their clinical care.

This investigator-led, non-commercial, non-interventional does not collect any patient identifiable information.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults (age ≥18 years) undergoing cardiac or thoracic surgery * With positive PCR in the 5 days before or after cardiac/thoracic surgery. Exclusion Criteria: * Minors

Primary outcome measure(s)

  • Highest VIS (Vasoactive-Inotropic Score) in the first 12 hours postoperatively. — 12 hours post-operatively
    The VIS score correlates with mortality after cardiac surgery and reflects the degree of patient hemodynamic failure. This score is calculated as follows: ISR = Dobutamine dose in g/kg/min + 100 times the Adrenaline dose in g/kg/min + 100 times the Noradrenaline dose in g/kg/min + 10,000 times the Vasopressin dose in U/kg/min.

Trial sites (1)

FacilityCityRegionStatus
University Hospital Nantes France Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT04389463 on ClinicalTrials.gov ↗ ← All trials in France