Status
Conditions
Treatments
About
This study is a prospective, single center, observational, cohort study of patients to determine whether the Mologic Biomarker Panel can identify patients with infection from those without, including those with other reasons for inflammation (e.g. post-operative). It will also assess whether it has the potential to judge the severity of illness, prognosticate outcome and guide antibiotic therapy.
The aim is to recruit patients who are "representative" of patients with suspected sepsis, uncomplicated infection, or non-infection related critical illness that require critical care intervention and assessment.
This study is observational and will not alter patient management or the standard of care. The results from the investigational Mologic Biomarker Panel and associated research assays will not be provided to treating clinicians, or used in any manner to affect patient care.
The study will take place over approximately an 18-month period and it is anticipated that approximately 600 patients will be collectively enrolled. The study aims to recruit patients from three environments within UCLH:
Enrollment
Sex
Ages
Volunteers
Inclusion criteria
Exclusion criteria
600 participants in 3 patient groups
Loading...
Central trial contact
Chris Dunston, PhD; John Wilkins, PhD
Data sourced from clinicaltrials.gov
Clinical trials
Research sites
Resources
Legal