Skip to main content
Clinical Trials/NCT01392508
NCT01392508CompletedNot Applicable

Prospective, Non-interventional, Multi-centre Clinical Study to Assess the Clinical Validity of the Heparin Binding Protein (HBP) Assay for Indicating the Presence, or Outcome, of Severe Sepsis (Including Septic Shock), Over 72 Hours, in Patients With Suspected Infection Following Emergency Department Admission.

Axis Shield Diagnostics Ltd5 sites in 2 countries759 target enrollmentStarted: March 2011Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Completed
Sponsor
Enrollment
759
Locations
5

Study Overview

Brief Summary

The purposes of this study is to determine whether Heparin Binding Protein (HBP) can be used as a marker of severe sepsis (including septic shock) in patients presenting to the emergency department with suspected infection.

Study Design

Study Type
Observational
Observational Model
Case Only
Time Perspective
Prospective

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Greater than or equal to 18 years
  • Suspected Infection
  • one or more SIRS criteria

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Axis Shield Diagnostics Ltd
Sponsor Class
Industry
Responsible Party
Sponsor

Study Sites (5)

Loading locations...

Similar Trials

IMproved PREdiction of Severe Sepsis in... | Clinical Trial