Patient Outcome of Cardiac Surgery During the COVID-19 Pandemic
Condition(s) studied
Investigational drug(s) / intervention(s)
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
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)
| Facility | City | Region | Status |
|---|---|---|---|
| University Hospital | Nantes | France | Recruiting |
More Nantes University Hospital trials in France
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