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Clinical Trial Summary

Prospective, multi-center, randomized, feasibility clinical study. Subjects will be randomized in a 1:1 ratio to either standard of care (SOC) alone or standard of care and treatment with the CytoSorb® device.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02566525
Study type Interventional
Source CytoSorbents, Inc
Contact
Status Completed
Phase N/A
Start date November 2015
Completion date December 2016

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