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

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

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON46211

Enrollment

500

Registered

2016-05-12

Start date

2018-02-20

Completion date

Unknown

Last updated

2024-04-23

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

Conditions

Stroke

Interventions

The intervention is not aimed at the patient but at the caregivers involved in acute stroke: direct visual feedback on the actual treatement delays for the patient they are transferring for IVT/IAT

Eligibility

Age

18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria: younger than 18 years

Design outcomes

Primary

Measure	Time frame
TSD to IAT and TSD to IVT.	—

Secondary

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

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)