BRAIN (Biomarker Rapid Assessment of Ischemic iNjury)
- Conditions
- Stroke Mimic(Conditions Presenting With Stroke-like Conditions)Stroke
- Registration Number
- NCT00206908
- Lead Sponsor
- Abbott RDx Cardiometabolic
- Brief Summary
This project is designed to evaluate the clinical utility of a novel blood test, the Triage Stroke Panel, as an aid in the diagnosis and assessment of stroke. The Triage Stroke Panel test device, used with the Triage MeterPlus, is a rapid, point-of-care immunoassay. The test measures the concentration of various analytes present in EDTA-anticoagulated whole blood or plasma, specifically B-type natriuretic peptide (BNP), fibrin degradation products containing D-Dimer, matrix metalloproteiase-9 (MMP-9), and S-100B. The test utilizes a proprietary algorithm for the automatic calculation of a single Multimarker Index (MMX) result from the individual biomarker values. The MMX result is being evaluated for use as an aid in the assessment and diagnosis of stroke.
- Detailed Description
To date, there is no commercially available blood test approved in the United States for use as an aid in the assessment and diagnosis of stroke. There have been various reports in the scientific literature describing the ability of various biomarkers to predict or identify stroke, with varied success. A biomarker panel approach, similar to that used for the evaluation of chest pain patients (troponin I, CK-MB, and myoglobin) enhances diagnostic accuracy, particularly when the panel includes protein markers associated with various components of the disease pathophysiology. This study involves a retrospective analysis of data collected from patients that present with an acute focal neurological deficit, suspected cerebral ischemia, or suspected intracranial hemorrhage within 24 hours of symptom onset or last known well time will be enrolled into the study. Blood samples will be collected at enrollment and serially up to 72 hrs. from the time of onset or last known well time. The study population will also include a subset of patients with subarachnoid hemorrhage, who will have additional samples collected daily from day 3 through day 14 (at clinical sites participating in the vasospasm substudy) for the evaluation of cerebral vasospasm. The patient's participation in the study is complete when all samples have been collected or when they are discharged from the hospital, whichever occurs first. All blood sample will be analyzed using the Triage Stroke Panel test. Measurements will be performed at each clinical site and at Biosite (subject to test device availability). In order to minimize bias and eliminate significant risk to the patient, physicians will be blinded to all Triage Stroke Panel results during the course of the study. Completed case report forms (CRFs) and frozen plasma samples will be transferred to Biosite.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 900
Age 18 and above Cerebral ischemia or intracranial hemorrhage suspected Enrollment within 24 hrs from symptom onset or last well-known time
None
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (22)
Hartford Hospital
πΊπΈHartford, Connecticut, United States
University of Pittsburgh
πΊπΈPittsburgh, Pennsylvania, United States
University of California, Los Angeles Medical Center
πΊπΈLos Angeles, California, United States
Hospital at the University of Pennsylvania
πΊπΈPhiladelphia, Pennsylvania, United States
Neurologische Universitatsklinik/Heidelberg
π©πͺHeidelberg, Germany
University of Massachusettes, Worcester Medical Center
πΊπΈWorcester, Massachusetts, United States
Cleveland Clinic Foundation
πΊπΈCleveland, Ohio, United States
OSF Saint Francis Medical Center
πΊπΈPeoria, Illinois, United States
Ingham Regional Medical Center
πΊπΈLansing, Michigan, United States
Toronto Western Hospital
π¨π¦Toronto, Ontario, Canada
Sentara Norfolk General Hospital
πΊπΈNorfolk, Virginia, United States
CHUV-Lausanne
π¨πLausanne, Switzerland
Alabama Neurological Institute
πΊπΈBirmingham, Alabama, United States
Henry Ford Health System
πΊπΈDetroit, Michigan, United States
Denver Health
πΊπΈDenver, Colorado, United States
University of Colorado Health Science Center
πΊπΈDenver, Colorado, United States
Kentucky Neuroscience Research
πΊπΈLouisville, Kentucky, United States
Henepin County Medical Center
πΊπΈMinneapolis, Minnesota, United States
St. Luke's Health System
πΊπΈKansas City, Missouri, United States
Duke University Hopsital
πΊπΈDurham, North Carolina, United States
University of Cincinnati
πΊπΈCincinnati, Ohio, United States
University of Nottingham
π¬π§Nottingham, United Kingdom