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Clinical Trial Summary

Extracorporeal life support (ECLS) is used as a last resort intervention in patients with severe cardiac, circulatory and/or respiratory failure with high (>80%) expected mortality. Despite considerable improvements in patient selection and outcomes, mortality and morbidity after ECLS remain high. An improved selection and management of patients who are supported with ECLS is therefore unquestionably needed from a perspective of optimal patient care and the socio-economic impact of this costly intervention.


Clinical Trial Description

This observational multicenter study was designed to serve the following objectives: 1. Develop a (dynamic) prediction tool for survival and quality of life outcomes 1 year after ECLS support for the situation at baseline and 7 days after ECLS initiation 2. Study the association between application of left ventricular unloading and ECLS support duration and weanability 3. Description of the incidence of VA ECLS weaning failure and identification of predictors for VA ECLS weaning failure Under this umbrella research protocol, the data collected by this observational multicenter study can also be reused for potential novel substudies with the objective to improve the quality of care and the efficiency of current treatment strategies involving ECLS. ;


Study Design


Related Conditions & MeSH terms

  • Extracorporeal Membrane Oxygenation
  • Extracorporeal Membrane Oxygenation Complication

NCT number NCT05444764
Study type Observational [Patient Registry]
Source UMC Utrecht
Contact Lara CA Pladet, MSc
Phone +31615466210
Email c.l.a.pladet@umcutrecht.nl
Status Recruiting
Phase
Start date September 16, 2021
Completion date March 1, 2024

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