Procalcitonin Monitoring Sepsis Study

NCT01523717 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 858

Last updated 2015-03-17

No results posted yet for this study

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.

Conditions

  • Severe Sepsis
  • Septic Shock

Sponsors & Collaborators

  • Brahms AG

    lead INDUSTRY

Principal Investigators

  • Nathan Shapiro, MD · Beth Israel Deaconess Medical Center

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-31
Primary Completion
2014-03-31
Completion
2014-03-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01523717 on ClinicalTrials.gov