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Diagnostic measure of atrial fibrillation on patients at outpatient TIA-clinic

Diagnostic measure of atrial fibrillation on patients at outpatient TIA-clinic - TIA-AF-project

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34100
Enrollment
50
Registered
2010-12-27
Start date
Unknown
Completion date
Unknown
Last updated
2024-05-06

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

Conditions

atrial fibrillation and ischemic stroke

Interventions

None listed

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: Ischemic stroke (CVA or TIA) signs and symptoms of atrial fibrillation left atrial enlargement at ECG left ventricle hypertrophy at ECG premature atrial complex at ECG hyperthyreoidie ischemic attacks in several cerebral flow area

Exclusion criteria

Exclusion criteria: atrial fibrillation in history atrial fibrillation registrated at ECG at outpatient clinic neurologie-TIA hemorragic CVA

Design outcomes

Primary

MeasureTime frame
Primary study parameters: - signs and symptoms fitting with atrial fibrillation (palpitations, short of breath, dizziness or chest pain) - left atrial enlargment at ECG - left ventriclehypertrophy at ECG - premature atrial heatbeats at ECG (with heartbeat > 70 bpm) - hyperthyreodie - cerebral ischemia in several flow areas Outcome: - atrial fibrillation—

Secondary

MeasureTime frame
no applied to—

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)