About this trial
In adult patients presenting to emergency departments within 24 hours of symptom onset with suspected acute stroke, we aim:
1. to identify early brain- and pathology-specific circulating, whole blood, plasma and serum panorOmic biomarkers that enable early acute stroke detection, diagnosis, dynamics, differentiation, monitoring, prediction and prognosis. 2. to identify early brain- and pathology-specific, panorOmic biomarkers in saliva that enable early acute stroke detection, diagnosis, dynamics, differentiation, monitoring, prediction and prognosis. 3. to derive biomarker platforms of models for early acute stroke detection, diagnosis, dynamics, differentiation, monitoring, prediction and prognosis 4. to validate these models in independent and external datasets
Eligibility criteria
Qualifiers
Adults ≥18 years of age.
Suspected acute stroke. Defined as either FAST-positive, or LAPSS-positive or ROSIER>0
Within 24 hours of symptom onset.
Informed consent.
Disqualifiers
Clear onset of acute symptoms >24 hours.
Trial design
Treatments tested in this trial
- Biomarker blood draw and saliva collection
Treatment groups
6
Treatment groupsSee each treatment group below.