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Effect of APC and Epo on the Inflammatory Response During Sepsis

Completed
Conditions
Systemic Inflammation
Sepsis
Registration Number
NCT00229034
Lead Sponsor
Lawson Health Research Institute
Brief Summary

An observational study to determine the effect of APC and Epo in reducing the systemic inflammatory response during severe sepsis.

Detailed Description

An observational study to determine the effect of APC and Epo in reducing the systemic inflammatory response during severe sepsis. Patients already prescribed either drug will be enrolled. The microcirculation of the sublingual vascular bed will be observed with a microscope to detect the alterations in the inflammatory response.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
40
Inclusion Criteria
  • patients in the ICU in severe septic shock undergoing APC and/or Epo treatment
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Exclusion Criteria
  • any severe comorbid conditions
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Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Lawson Health Research Institute

🇨🇦

London, Ontario, Canada

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