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Stroke Triage Optimization by Ambulance Paramedics in the Pre-hospital Setting

Comparison of Prehospital Stroke Screening Scales in the Ambulance Setting; a Multiregional, Multicenter Observational Cohort Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06332989
Acronym
STROKE-APP
Enrollment
3000
Registered
2024-03-27
Start date
2024-02-01
Completion date
2027-02-01
Last updated
2024-03-27

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

Conditions

Pre-hospital Triage, Stroke, Acute, Stroke Code, Stroke Treatment

Brief summary

There are everal scales designed to help ambulance paramedics to identify a patient with a stroke and activate a stroke code. These scales were never tested in the field in a large unselected patient sample. We aim to perform an in-the field head tot head comparison of all published stroke scales designed to be used by ambulance paramedics

Detailed description

this is a multicenter multiregional cohort study including about 3000 stroke code patients. In all patients an application will be filled out before hospital arrival including items that enable us to reconstruct all previously published stroke scales. Data from the application will be related to in hospital data of the same patient. In order to do this we will use a trusted third party for data coupling.

Interventions

OTHERstroke-APP

Ambulane paramedics will use an online application to fill in several observations on scen

Sponsors

Alrijne Ziekenhuis Leiderdorp
CollaboratorNETWORK
Groene Hart Ziekenhuis
CollaboratorOTHER
Medical Center Haaglanden
CollaboratorOTHER
HagaZiekenhuis
CollaboratorOTHER
Reinier de Graaf Groep
CollaboratorOTHER
Regionale Ambulance Voorziening Hollands Midden
CollaboratorOTHER
Leiden University Medical Center
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* patients for whom a stroke code is activated

Exclusion criteria

\< 18 years

Design outcomes

Primary

MeasureTime frameDescription
final diagnosisdischarge or after 3 monthsDiangosis by treating physician
treated with reperfusion therapyfirst 24 hours after admissiontreatment with IV thrombolysis; endovascular therapy or surgery
additional investigationson admissionCT scans performed

Countries

Netherlands

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026