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Japan Intensive Care ECMO Consortium: Nationwide Effort for ECMO Care Optimization and eXcellence sTudy

Japan Intensive Care ECMO Consortium: Nationwide Effort for ECMO Care Optimization and eXcellence sTudy - ECMO NEXT study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-jRCT1040240168
Enrollment
2500
Registered
2025-01-17
Start date
2018-01-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Extracorporeal Membrane Oxygenation Extracorporeal Membrane Oxygenation

Interventions

none

Sponsors

Kasugai Daisuke
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Between January 1, 2018, and December 31, 2023, individuals meeting the following criteria: Aged 18 years or older Required ECMO management in the intensive care unit of Nagoya University Hospital or Participating sites

Exclusion criteria

Exclusion criteria: None (Appropriate exclusion criteria will be defined for each specific clinical question.

Design outcomes

Primary

MeasureTime frame
Weaning failure within 30 days of ECMO decannulation, which is a composite of death, ECMO reinitiation, or bridging to transplantation (left ventricular assist device or heart/lung transplantation) Inhospital moratality

Secondary

MeasureTime frame
Laboratory data. CT Imaging. Functional outcomes were assessed using standardized scales, including the Johns Hopkins Safe Patient Handling Mobility, Barthel Index, ICU Mobility Scale, Medical Research Council Score, and Clinical Frailty Scale. These assessments were performed at three specific time points: ICU discharge, seven days after ICU discharge, and hospital discharge.

Contacts

Public ContactDaisuke Kasugai

Department of Emergency and Clinical Care Medicine

dkasugai@med.nagoya-u.ac.jp+81-52-741-2111

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026