Retrospective Cohort Study of Low-Flow Extracorporeal Carbon Dioxide Removal (ECCO2R) System: Evaluating ECCO2R's Efficacy and Safety in Participants With Respiratory Failure

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorHong Kong University

About this trial

This is an observational study performed by retrospective review of data routinely collected for patients receiving low-flow extracorporeal carbon dioxide removal (ECCO2R) therapy in intensive care units (ICUs). Our aim is to firstly, describe the local practice in terms of patient selection and technical details of clinical management related to the use of low-flow ECCO2R system, and secondly, the clinical results in terms of patient outcomes and adverse events. These findings may allow clinicians to improve the quality and safety of ECCO2R therapy provision in the ICU.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients supported with ECCO2R in one of the designated study sites

Admitted to the ICU between 1 Jan 2022 and 30 June 2024

Disqualifiers

Patients younger than 18 years old

Trial population

Patients supported with ECCO2R in our designated study sites

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

59 Participants
are grouped into 1 trial group
Group A: Patients with respiratory failure and supported with ECCO2R

Trial outcomes

Primary outcomes

1

Around 60 participants with respiratory failure as assessed for their clinical characteristics and outcomes

The primary endpoint is to describe the patients' demographics (e.g. Age, Sex), clinical characteristics (e.g. APACHE score, ventilator using time, respiratory parameters, ventilatory parameters, Mortality), outcomes of patients (death or survive) who received ECCO2R therapy. The secondary endpoints are to evaluate the association between clinical factors and patient outcomes (e.g. life of stay in ICU, ventilator free days), and to identify potential risk factors for adverse events and complications.

Time frame
From November 2024 to September 2026 (Anticipated)

Secondary outcomes

Other outcomes

Sponsors and contacts

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Hong Kong University

Lead sponsor

Hospital Authority, Hong Kong

Sponsor institution