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Procalcitonin Monitoring Sepsis Study — MOSES  

Septic Shock Clinical Trial

Official title:
Procalcitonin Decrease Over 72 Hours and Outcome in Patients With Severe Sepsis or Septic Shock

Clinical Trial Summary

The purpose of this study is to investigate the relationship between a procalcitonin decrease over 72 hours and outcome in patients who have severe sepsis or septic shock.

Clinical Trial Description

n/a

Study Design

Observational Model: Case-Only, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT01523717
Study type Observational
Source Brahms AG
Contact
Status Completed
Phase N/A
Start date December 2011
Completion date March 2014
View Details
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