Prognosis of Veno-Venous Extracorporeal Membrane Oxygenation in Emergency Thoracic Surgery
Recruiting now
Conditions studied: VV-ECMO, Thoracic Surgery, Emergency Surgery, ARDS, Retrospective Cohort, Propensity Score Matching, Mortality, ECMO Outcomes
In brief
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).
Key facts
- Study ID
- NCT07016685
- Run by
- Centre Hospitalier Universitaire, Amiens
- People needed
- 380
- Starts
- 2025-06-01
- Expected to finish
- 2026-04-01
- Last updated by the study team
- 2025-06-13
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Adults ≥ 18 years
- VV-ECMO initiated during or after emergency thoracic surgery
- No opposition to data use
You may not qualify if…
- Pregnant women
- Veno-Arterial ECMO patients
- Patients under legal protection
Where it is running
- CHRU Amiens — Amiens, France (enrolling)
Full record on ClinicalTrials.gov
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