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Clinical trial intelligence report
CytOSorb TreatMent Of Critically Ill PatientS Registry: International Registry on the Use of CytoSorb in the Critical Care Setting
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 16, 2026
NCT ID
NCT05146336
Status
RECRUITING
Phase
Observational Registry
Sponsor
CytoSorbents, Inc
Executive brief
Investment-Ready Snapshot
The COSMOS registry, sponsored by CytoSorbents, Inc., aims to establish a comprehensive data repository for the use of the CytoSorb device in critical care settings. This initiative is expected to enhance the understanding of the device's efficacy in real-world applications, particularly in conditions such as septic shock and acute respiratory distress syndrome. The registry's findings could strengthen CytoSorbents' market position by providing robust clinical evidence to support the device's use, potentially leading to increased adoption in critical care units. The competitive landscape includes other hemoperfusion devices, but the unique focus on cytokine removal may provide a differentiated value proposition. Diligence considerations should include the regulatory landscape and potential reimbursement pathways for the device.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT05146336
Indication
Septic Shock
Modality
medical device
Target
CytoSorb device for hemoperfusion therapy targeting cytokine removal in critically ill patients.
Intervention
CytoSorb
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.