Hemoadsorption Therapy in Critically Ill Adults

Is this trial a fit for you?

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

This is a single-center retrospective observational study conducted at Flór Ferenc Hospital in Kistarcsa, Hungary. It analyzes adult ICU patients who received CytoSorb or Efferon LPS hemoadsorption between January 1, 2020 and May 31, 2026. The researchers will compare pre- and post-treatment data on vasopressor needs, hemodynamics, inflammatory and liver biomarkers, tissue perfusion, and oxygenation, and will report ICU length of stay as well as ICU, 28-day, and 90-day mortality. No interventions are performed as part of the study; data are collected from anonymized medical records. The goal is to clarify how hemoadsorption might affect outcomes in septic shock and other hyperinflammatory states.

Why it matters

Who can join: the full rules

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.

Where it's running

• Pest County Flór Ferenc Hospital, Dept. of Anaesthesiology and Intensive Therapy
  Kistarcsa, Pest County, Hungary Recruiting

Study contacts

• Study coordinator: Zoltán Ruszkai, MD, PhD
• Email: ruszkai.zoltan@florhosp.hu
• Phone: 0036209151978

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How to take part

1. Review the eligibility criteria above with your treating physician.
2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.