Cardiac Event Monitoring in the Acute inpatient Setting of Ischemic Stroke.

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

NL-OMON

Registry ID

NL-OMON20289

Enrollment

150

Registered

2011-07-14

Start date

2011-07-11

Completion date

Unknown

Last updated

2024-02-28

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

Conditions

Atrial Fibrillation, Ischemic Stroke

Interventions

24 hours event monitoring in ischemic stroke patients.

Eligibility

Inclusion criteria

Inclusion criteria: Patients with current ischemic stroke.

Exclusion criteria

Exclusion criteria: Prior documented paroxysmal, persistent or chronic atrial fibrillation.

Design outcomes

Primary

Measure	Time frame
The incidence of atrial fibrillation in the acute setting of ischemic stroke.	—

Secondary

Measure	Time frame
1. The incidence of atrial fibrillation in increased body-mass-index; 2. The incidence of atrial fibrillation in symptomatic patients; 3. The incidence of accelerated atrial activity < 30 seconds.	—

Contacts

Public ContactB. Oude Velthuis

Postbus 50000

b.oudevelthuis@mst.nl+31 (0)53 4872110

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)