NCT07016685

Brief 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).

Trial Health

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Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
380

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2025

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 29, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

June 1, 2025

Completed
11 days until next milestone

First Posted

Study publicly available on registry

June 12, 2025

Completed
5 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

November 1, 2025

Completed
5 months until next milestone

Study Completion

Last participant's last visit for all outcomes

April 1, 2026

Completed
Last Updated

June 13, 2025

Status Verified

June 1, 2025

Enrollment Period

5 months

First QC Date

April 29, 2025

Last Update Submit

June 12, 2025

Conditions

Keywords

thoracic surgeryVV-ECMOemergency surgeryARDSretrospective cohortpropensity score matchingmortalityECMO outcomes

Outcome Measures

Primary Outcomes (1)

  • 90-day all-cause mortality

    90 days

Secondary Outcomes (2)

  • 90-day mortality in oncologic vs. non-oncologic thoracic surgery

    90 days

  • Postoperative complication rates

    90 days

Study Arms (2)

VV-ECMO after emergency thoracic surgery

VV-ECMO after emergency thoracic surgery

VV-ECMO for medical ARF

VV-ECMO for medical indication

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

Adults ≥ 18 years, Patients undergoing emergency thoracic procedures requiring VV-ECMO and patients treated with VV-ECMO for medical respiratory failure.

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

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

CHRU Amiens

Amiens, 80480, France

RECRUITING

Related Publications (1)

  • Beyls C, Soulier-Zaninka Q, Georges O, Nguyen M, Dheilly T, Nicolas M, Huette P, De Dominicis F, Abou-Arab O, Guinot PG, Mahjoub Y. Perioperative Veno-Venous Extracorporeal Membrane Oxygenation in Non-Elective Thoracic Surgery: A Propensity-Matched Bicentric Comparison With Medical Indication. Interdiscip Cardiovasc Thorac Surg. 2025 Nov 6;40(11):ivaf255. doi: 10.1093/icvts/ivaf255.

Central Study Contacts

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
RETROSPECTIVE
Sponsor Type
OTHER
Responsible Party
SPONSOR

Study Record Dates

First Submitted

April 29, 2025

First Posted

June 12, 2025

Study Start

June 1, 2025

Primary Completion

November 1, 2025

Study Completion

April 1, 2026

Last Updated

June 13, 2025

Record last verified: 2025-06

Data Sharing

IPD Sharing
Will not share

Locations