Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
74 participants
OBSERVATIONAL
2022-01-01
2025-11-30
Brief Summary
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Detailed Description
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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.
Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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Retrospective eCPR group
Retrospective analysis of eCPR patients
Retrospective analysis of assigned treatment
Retrospective analysis of assigned treatment will be performed
Prospective eCPR group
Prospective analysis of eCPR patients
Hospital Anxiety and Depression (HADS)
Hospital Anxiety and Depression will be assessed using the HADS (Hospital Anxiety and Depression Scale)
Quality of Life (SF-36)
The quality of life will be assessed using the SF-36 (Short-Form Health Subject Questionnaire).
Quality of Life (EQ-5D)
The quality of life will be assessed using the EQ-5D (European Quality of Life Questionnaire)
Interventions
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Hospital Anxiety and Depression (HADS)
Hospital Anxiety and Depression will be assessed using the HADS (Hospital Anxiety and Depression Scale)
Quality of Life (SF-36)
The quality of life will be assessed using the SF-36 (Short-Form Health Subject Questionnaire).
Quality of Life (EQ-5D)
The quality of life will be assessed using the EQ-5D (European Quality of Life Questionnaire)
Retrospective analysis of assigned treatment
Retrospective analysis of assigned treatment will be performed
Eligibility Criteria
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Inclusion Criteria
* 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
* Acute serious mental or somatic disease making the interview not feasible
18 Years
ALL
No
Sponsors
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University Hospital Ostrava
OTHER
Responsible Party
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Principal Investigators
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Michaela Lišková, Bc.
Role: PRINCIPAL_INVESTIGATOR
University of Ostrava
Locations
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University of Ostrava
Ostrava, Moravian-Silesian Region, Czechia
University Hospital Ostrava
Ostrava, Moravian-Silesian Region, Czechia
Countries
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Other Identifiers
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FNO-KARIM-eCPR
Identifier Type: -
Identifier Source: org_study_id
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