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.