Skip to content

Evaluation of a new fingerprick blood test for the identification of serious stroke

Rapid Assay Diagnostic for Acute stroke Recognition (RADAR)

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN12414986
Enrollment
552
Registered
2023-05-02
Start date
2023-06-01
Completion date
Unknown
Last updated
2026-06-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suspected acute stroke Circulatory System Stroke, not specified as haemorrhage or infarction

Interventions

This research project is a prospective observational cohort study to evaluate the diagnostic accuracy of a new fingerprick blood test for the identification of LVO stroke. The fingerprick test measu

Sponsors

Northumbria Healthcare NHS Foundation Trust
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 110 Years

Inclusion criteria

Inclusion criteria: 1. Aged 18 years or over 2. Arrived at the study hospital by emergency ambulance 3. New acute stroke suspected by ambulance personnel before hospital arrival 4. FAST clinical symptom score is =1 (as determined by hospital staff) 5. Stroke symptoms are known to have begun within the last 6 hours OR the patient was last known to be well between 6 and 24 hours ago (times determined by hospital specialist staff) 6. Blood sampling can be undertaken prior to any reperfusion treatments 7. Routine brain imaging is intended to be urgently performed

Exclusion criteria

Exclusion criteria: 1. Already assessed at another hospital and ambulance admission is a transfer for continuing care 2. Assigned a recent previous (within the last 4 weeks) diagnosis of deep vein thrombosis, pulmonary embolism, arterial embolism, stroke, TIA, long bone fracture, major trauma, any surgery under general anaesthesia (these diagnoses may have resulted in elevated d-dimer) 3. Suffered a recent previous (within the last 4 weeks) head injury which lead to hospital attendance (this event may have resulted in elevated GFAP) 4. Stroke symptoms are known to have begun greater than 6 hours ago

Design outcomes

Primary

MeasureTime frame
Sensitivity, specificity, positive and negative predictive values for identification of LVO stroke calculated from the new fingerprick blood test result and reference standard tests.

Secondary

MeasureTime frame
Secondary objectives/analyses will examine the accuracy of the fingerprick test using different analysis populations

Countries

England, United Kingdom

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Jun 11, 2026