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CytOSorb TreatMent Of Critically Ill PatientS Registry

Recruitingn/aAges any - anyAllCytoSorbents, Inc
NCT05146336 on ClinicalTrials.gov ↗
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In plain words

What the trial is, and whether it could suit you

Registry intended to provide a data repository and reporting infrastructure for the surveillance of CytoSorb device use in real-world critical care settings, and to serve as an objective, comprehensive, and scientifically-based resource to measure and improve the quality of patient care

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

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📋 Eligibility rules (as published)
Inclusion Criteria: 1. Planned OR actual CytoSorb® 300 mL device utilization 2. Informed consent for prospective registry participation Exclusion Criteria: 1. Use of the CytoSorb® 300 mL device for antithrombotic removal only 2. Intraoperative use of CytoSorb® 300 mL device during cardiac surgery only 3. The occurrence of a complication or other medically justified circumstance that arises after written informed consent has been obtained from the patient and before or during the planned therapy and as a result of which the use of CytoSorb® 300 mL Adsorber is contraindicated or no longer appropriate.
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What it tests

  • CytoSorb
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Where

28 sites
Klinikum Klagenfurt am Wörthersee
Klagenfurt, Austria
Medizinische Universität Wien
Vienna, Austria
Universitätsklinikum Aachen
Aachen, Germany
Herz- und Diabeteszentrum Nordrhein-Westfalen
Bad Oeynhausen, Germany
Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil Bochum
Bochum, Germany
Katholisches Klinikum Bochum, St. Josef-Hospital
Bochum, Germany
Universitätsklinikum Essen, Medizinische Intensivtherapie
Essen, Germany
Universitätsklinikum Essen, Nephrologie
Essen, Germany

…and 20 more on ClinicalTrials.gov.

🤝 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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