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Clinical Trials in France / NCT07016685
Recruiting Observational

Prognosis of Veno-Venous Extracorporeal Membrane Oxygenation in Emergency Thoracic Surgery

NCT07016685 · tracked via the Priya Life Science France tracker
Sponsor
Centre Hospitalier Universitaire, Amiens
Phase
Observational
Started
2025-06-01
Last updated
2025-06-13

Condition(s) studied

VV-ECMOThoracic SurgeryEmergency SurgeryARDSRetrospective CohortPropensity Score MatchingMortalityECMO Outcomes

Study summary

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).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Adults ≥ 18 years * VV-ECMO initiated during or after emergency thoracic surgery * No opposition to data use Exclusion Criteria: * Pregnant women * Veno-Arterial ECMO patients * Patients under legal protection

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
CHRU Amiens Amiens France Recruiting

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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 NCT07016685 on ClinicalTrials.gov ↗ ← All trials in France