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Recruiting NCT06332989

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

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

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: stroke-APP.
Who it may be relevant to
Registry conditions: Stroke, Acute, Pre-hospital Triage, Stroke Treatment, Stroke Code. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Netherlands
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

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

Overview

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

  • Other stroke-APP
    Ambulane paramedics will use an online application to fill in several observations on scen

Primary outcome measures

  • final diagnosis [Time frame: discharge or after 3 months]
  • treated with reperfusion therapy [Time frame: first 24 hours after admission]
  • additional investigations [Time frame: on admission]

Eligibility criteria

Inclusion criteria

  • patients for whom a stroke code is activated

Exclusion criteria

< 18 years

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

Netherlands · 1 center
  • Leiden University medical center — Leiden

Identifiers

NCT: NCT06332989 · N22.129

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗