Clinical Trials Directory

Trials / Completed

CompletedNCT01392508

IMproved PREdiction of Severe Sepsis in the Emergency Department

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.

Status
Completed
Phase
Study type
Observational
Enrollment
759 (actual)
Sponsor
Axis Shield Diagnostics Ltd · Industry
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

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.

Conditions

Timeline

Start date
2011-03-01
Primary completion
2015-09-01
Completion
2015-09-01
First posted
2011-07-12
Last updated
2017-04-14

Locations

5 sites across 2 countries: United States, Sweden

Source: ClinicalTrials.gov record NCT01392508. Inclusion in this directory is not an endorsement.

IMproved PREdiction of Severe Sepsis in the Emergency Department (NCT01392508) · Clinical Trials Directory