A REDUCTION IN TIME WITH ELECTRONIC MONITORING IN STROKE TRIAL (ARTEMIS Trial).

Completed

• Conditions: Stroke; brain infarction; 10007963

• Registration Number: NL-OMON46211
• Lead Sponsor: eurologie

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 23 April 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 500

Inclusion Criteria

All patients with suspected stroke potentially eligible for IVT and/or IAT for whom the dispatch office send out an ambulance.

Exclusion Criteria

younger than 18 years

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>TSD to IAT and TSD to IVT. </p><br>

Secondary Outcome Measures

Name	Time	Method
<p>- the proportion of patients finally treated with IVT /IAT calculated from:<br /><br>- the total of patients for whom the ambulance issues a dispatch<br /><br>- the total of patients transferred to the hospital with suspected stroke<br /><br>- the total of patients with a final diagnosis of (ischemic) stroke<br /><br>- functional outcome at three-months measured by telephone with the modified<br /><br>Rankin scale</p><br>