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Ambulance feasibility study of a rapid blood test for stroke

Rapid Ambulance DIagnosis Of Stroke (RADIOS): a pre-hospital feasibility study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN12803526
Enrollment
30
Registered
2024-05-03
Start date
2024-07-01
Completion date
Unknown
Last updated
2024-06-18

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

Conditions

Suspected stroke Nervous System Diseases

Interventions

The intervention associated to this study is performing the LVOne test, which, from the patient perspective, involves collecting a fingerstick blood sample and testing with the device. The total obser

Sponsors

Pockit diagnostics Ltd, T/A Upfront diagnostics
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1. Attended by study trained ambulance clinician 2. Evaluated for suspected acute stroke 3. Within 6 hours of symptom onset 4. Age >18 years 5. Local hospital is Cambridge University Hospital (or other thrombectomy-capable hospital)

Exclusion criteria

Exclusion criteria: 1. Witnessed seizure at presentation 2. Hypoglycaemia, (blood glucose <3mmol/l) 3. Severe frailty or limited life expectancy <6 months 4. Patient is not conveyed to Cambridge University Hospital (or other thrombectomy-capable hospital)

Design outcomes

Primary

MeasureTime frame
Expert opinions on the feasibility of the LVOne test during routine ambulance visits. The method used to collect this data is qualitative evaluation in the form of a questionnaire.

Secondary

MeasureTime frame
There are no secondary outcome measures

Countries

England, United Kingdom

Contacts

Public ContactEdoardo Gaude
edoardo.gaude@pockitdx.co.uk+44 1223 363608

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026