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
25 participants
OBSERVATIONAL
2017-06-01
2021-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Study Groups
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Veno-arterial ECMO patients
Patients with severe SIRS post extracorporeal cardiopulmonary resuscitation (ECPR) or accompanying cardiogenic shock who were treated with hemoadsorption.
No interventions assigned to this group
Veno-venous ECMO patients
Patients with refractory septic shock on VV ECMO who were treated with hemoadsorption.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* hemoadsorption
* Age ≥ 18 years
18 Years
ALL
No
Sponsors
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University Medical Centre Ljubljana
OTHER
Responsible Party
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Jernej Berden
Jernej Berden, MD, PhD
Locations
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University Medical Center Ljubljana
Ljubljana, , Slovenia
Countries
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Other Identifiers
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Haemoadsorption ECMO
Identifier Type: -
Identifier Source: org_study_id
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