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Hemodynamic, Laboratory, and Clinical Outcomes of Hemoadsorption Therapy

Recruitingn/aAges 18 Years - anyAllPest County Flór Ferenc Hospital
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In plain words

What the trial is, and whether it could suit you

This single-center retrospective observational cohort study aims to evaluate the clinical, hemodynamic, and laboratory effects of adjunctive hemoadsorption therapy in critically ill adult patients treated in the Intensive Care Unit of Flór Ferenc Hospital, Hungary, between January 1, 2020, and May 31, 2026. Patients who received CytoSorb® or Efferon LPS® hemoadsorption therapy will be included. The study will assess changes in vasopressor requirements, hemodynamic parameters, inflammatory biomarkers, liver function tests, tissue perfusion markers, and oxygenation following hemoadsorption treatment. Clinical outcomes, including intensive care unit length of stay, all-cause mortality occurring during the patient's stay in the intensive care unit (ICU mortality), and 28-day and 90-day mortality, will also be evaluated. Data will be collected retrospectively from anonymized medical records,

Sign in to get the eligibility rules as simple questions to take to your doctor.

📋 Eligibility rules (as published)
Inclusion Criteria: * \>18 years; * CytoSorb or Efferon LPS hemoadsorption treatment, * with available relevant pre- and post-treatment clinical and laboratory data Exclusion Criteria: * age under 18 years * missing key demographic or outcome data; * unknown treatment type or timing; * data unavailable for legal or ethical reasons.
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What it tests

  • Hemoadsorption
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Where

1 site
Pest County Flór Ferenc Hospital, Dept. of Anaesthesiology and Intensive Therapy
Kistarcsa, Hungary
🤝 Taking part is your choice, and you can leave at any time. Only the trial team can confirm you are eligible — always decide together with your own doctor.
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