Impact of the Implementation of a Referral Veno-venous Extracorporeal Membrane Oxygenation Centre on Mortality

Completed

• Conditions: Extracorporeal Membrane Oxygenation

• Registration Number: NCT05154071
• Lead Sponsor: Centre Hospitalier Universitaire Dijon

Brief Summary

Current evidence suggest that regrouping patient supported by veno-venous ECMO in high-volume centre could improve outcome. A dedicated ECMO unit was implemented in Dijon.

The objective of the present study was to evaluate the implementation of this unit. The hypothesis was that patient taken care within this structured care system would have lower mortality.

This research comprises a retrospective observational study conducted in Dijon university hospital

Detailed Description

Not available

Study Timeline

• Status Verified: 2021-10
• Study Start: 2021-10-01
• Study First Submitted: 2021-10-21
• Primary Completion: 2021-11-01
• Study Completion: 2021-12-01
• Study First Submitted QC: 2021-12-09
• Last Update Submitted: 2021-12-09
• Study First Posted: 2021-12-10
• Last Update Posted: 2021-12-10

Recruitment & Eligibility

• Status: COMPLETED
• Sex: All
• Target Recruitment: 172

Inclusion Criteria

• patient in an adult Dijon ICUs supported by veno-venous ECMO
• patient hospitalized between January the 1st 2011 and June the 30th 2021

Exclusion Criteria

• Refusal to participate,
• patient admitted to pediatric ICU

Study & Design

• Study Type: OBSERVATIONAL
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Mortality rate	90 days

Secondary Outcome Measures

Name	Time	Method
Rate of ECMO adverse events	through study completion, an average of 3 years
Hospital length of stay	through study completion, an average of 3 years
ICU length of stay	through study completion, an average of 3 years

Trial Locations

Locations (1)

Chu Dijon Bourogne; 🇫🇷 Dijon, France