Actively Recruiting
Prognosis of Veno-Venous Extracorporeal Membrane Oxygenation in Emergency Thoracic Surgery
Led by Centre Hospitalier Universitaire, Amiens · Updated on 2025-06-13
380
Participants Needed
1
Research Sites
43 weeks
Total Duration
On this page
Sponsors
C
Centre Hospitalier Universitaire, Amiens
Lead Sponsor
C
Centre Hospitalier Universitaire Dijon
Collaborating Sponsor
AI-Summary
What this Trial Is About
Veno-vneous extracorporeal membrane oxygenation (VV-ECMO) is an established support strategy for acute respiratory failure, but its role in the perioperative management of emergency thoracic surgery remains poorly defined. This retrospective, multicenter, observational study aims to assess the clinical outcomes and prognostic factors in this high-risk population. Patients undergoing emergency thoracic procedures requiring VV-ECMO will be compared to a control cohort of patients treated with VV-ECMO for medical respiratory failure. Data will be collected from two French academic centers (CHU Amiens-Picardie and CHU Dijon).
CONDITIONS
Official Title
Prognosis of Veno-Venous Extracorporeal Membrane Oxygenation in Emergency Thoracic Surgery
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults 18 years or older
- VV-ECMO started during or after emergency thoracic surgery
- No opposition to the use of medical data
You will not qualify if you...
- Pregnant women
- Patients receiving veno-arterial ECMO
- Patients under legal protection such as guardianship or conservatorship
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
CHRU Amiens
Amiens, France, 80480
Actively Recruiting
Research Team
C
Christophe Beyls, MD
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
2
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