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Treatment Outcome in Patients After eCPR

Treatment Outcome in Patients After eCPR

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07031466
Enrollment
74
Registered
2025-06-22
Start date
2022-01-01
Completion date
2025-11-30
Last updated
2025-12-05

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

Conditions

Cardiac Arrest (CA)

Keywords

extracorporeal membrane oxygenation (ECMO), extracorporeal cardiopulmonary resuscitation (eCPR), Quality of Life, out-of-hospital cardiac arrest (OHCA), Post-Intensive Care Syndrome (PICS)

Brief summary

This study consists of two parts - retrospective and prospective. The aim of this study is to assess the quality of life in bio-psycho-social dimensions in patients after eCPR (extracorporeal cardiopulmonary resuscitation), in relation to their neurological outcome after the end of treatment and discharge from the Ostrava University Hospital (FNO). The study will focus on patients who underwent extracorporeal membrane oxygenation (ECMO) support after out-of-hospital cardiac arrest (OHCA) in the years 2022-2024.

Detailed description

Retrospective study Quantitative evaluation using data analysis from documentation. Patients on ECMO after OHCA in the period 1. 1. 2022 - 31. 12. 2024 will be evaluated based on data from the documentation. Analysis of data from the documentation of selected patients will be performed, evaluating demographic data, comorbidities, duration of ECMO support, mortality, Cerebral Performance Category (CPC) score 30 days after CPR. Prospective study Quantitative assessment using validated questionnaire tools Patients connected to ECMO after OHCA in the period 1. 1. 2022 - 31. 12. 2024, in whom a CPC score \>3 was detected after the 30th day from cardiac arrest and who were discharged from the FNO. As part of patient dispensary, these patients are electively invited to the PICS outpatient clinic in the FNO Ostrava. Individual interviews (filling out questionnaires) will be performed after obtaining informed consent in the Post-Intensive Care Syndrome (PICS) outpatient clinic at the University Hospital Ostrava, or telephone interviews conducted by the attending physician.

Interventions

Retrospective analysis of assigned treatment will be performed

OTHERQuality of Life (SF-36)

The quality of life will be assessed using the SF-36 (Short-Form Health Subject Questionnaire).

OTHERQuality of Life (EQ-5D)

The quality of life will be assessed using the EQ-5D (European Quality of Life Questionnaire)

OTHERHospital Anxiety and Depression (HADS)

Hospital Anxiety and Depression will be assessed using the HADS (Hospital Anxiety and Depression Scale)

Sponsors

University Hospital Ostrava
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Patient who underwent eCPR after OHCA at University Hospital Ostrava * Hospitalised in the period from 1. 1. 2022 to 31. 12. 2024 * Ability to undergo an interview personally or a family member able to provide information * Signed informed consent

Exclusion criteria

* Language barrier * Acute serious mental or somatic disease making the interview not feasible

Design outcomes

Primary

MeasureTime frameDescription
Quality of Life (SF-36)30 daysQuality of Life in patients after eCPR will be assessed using the SF-36 questionnaire 30 days after eCPR
Quality of Life (EQ-5D)30 daysQuality of Life in patients after eCPR will be assessed using the EQ-5D questionnaire 30 days after eCPR
Hospital Anxiety and Depression Scale (HADS)30 daysHospital Anxiety and Depression Scale (HADS) in patients after eCPR will be assessed using the EQ-5D questionnaire 30 days after eCPR

Countries

Czechia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026