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Safety and Efficacy of Polymyxin B Hemoperfusion (PMX) for Septic Shock — EUPHRATES  

Septic Shock Clinical Trial

Official title:
Evaluating the Use of Polymyxin B Hemoperfusion in a Randomized Controlled Trial of Adults Treated for Endotoxemia and Septic Shock

Clinical Trial Summary

To compare the safety and efficacy of the PMX cartridge based on mortality at 28-days in subjects with septic shock who have high levels of endotoxin and are treated with standard medical care plus use of the PMX cartridge, versus subjects who receive standard medical care alone.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01046669
Study type Interventional
Source Spectral Diagnostics (US) Inc.
Contact
Status Completed
Phase N/A
Start date June 2010
Completion date June 2017
View Details
See also
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