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A RCT to Assess the Performance of CytoSorb for Shock Reversal in Patients With Vasoplegic Septic Shock — PROCYSS  

Septic Shock Clinical Trial

Official title:
A Prospective, Randomized, Multicenter, Single-blind, Controlled Study to Assess the Performance of the Cytosorb® 300 ml Device for Shock Reversal in Patients With Vasoplegic Septic Shock

Clinical Trial Summary

To assess the performance of the CytoSorb® 300 mL device for shock reversal in patients with vasoplegic septic shock.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04963920
Study type Interventional
Source CytoSorbents Europe GmbH
Contact Antje Fechner
Phone +49 30 654 99 145
Email procyss@cytosorbents.com
Status Recruiting
Phase N/A
Start date January 30, 2022
Completion date May 2025
View Details
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