Clinical Trials Directory

Trials / Unknown

UnknownNCT05444764

PREdiCtIon of Weanability, Survival and Functional outcomEs After ECLS

Status
Unknown
Phase
Study type
Observational
Enrollment
800 (estimated)
Sponsor
UMC Utrecht · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Detailed 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.

Conditions

Timeline

Start date
2021-09-16
Primary completion
2024-03-01
Completion
2024-03-01
First posted
2022-07-06
Last updated
2024-01-05

Locations

6 sites across 1 country: Netherlands

Source: ClinicalTrials.gov record NCT05444764. Inclusion in this directory is not an endorsement.