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Study identifier: NCT05146336 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

CytOSorb TreatMent Of Critically Ill PatientS Registry

Condition: Septic Shock · Acute Respiratory Distress Syndrome · Trauma  ·  Sponsor: CytoSorbents, Inc

PhaseN/A
Planned participants3000
Who can joinAll sexes, N/A to no upper limit
Healthy volunteersNo

About this study

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

This description comes directly from the study's public registry record.

Talk to the study team

Robert Wilke  ·  +49 30 654 99 145  ·  cosmos@cytosorbents.com

Always discuss trial participation with your own doctor first.

Locations (28)

Klinikum Klagenfurt am WörtherseeKlagenfurt, AustriaRecruiting
Medizinische Universität WienVienna, AustriaRecruiting
Universitätsklinikum AachenAachen, GermanyRecruiting
Herz- und Diabeteszentrum Nordrhein-WestfalenBad Oeynhausen, GermanyRecruiting
Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil BochumBochum, GermanyRecruiting
Katholisches Klinikum Bochum, St. Josef-HospitalBochum, GermanyRecruiting
Universitätsklinikum Essen, Medizinische IntensivtherapieEssen, GermanyRecruiting
Universitätsklinikum Essen, NephrologieEssen, GermanyRecruiting
Universitätsklinikum Essen, Thorax- und Kardiovaskuläre ChirurgieEssen, GermanyRecruiting
Universitätsmedizin Göttingen, Allgemein-, Viszeral- und KinderchirurgieGöttingen, GermanyRecruiting
Universitätsmedizin Göttingen, Herzzentrum GöttingenGöttingen, GermanyRecruiting
Klinikum HerfordHerford, GermanyRecruiting

+ 16 more locations — full list on the registry record.

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Source record: clinicaltrials.gov/study/NCT05146336