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Diagnostic of atrial fibrillation on patients at TIA-clinic

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

Status
Unknown
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34477
Enrollment
50
Registered
2010-09-10
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

Interventions

None listed

Sponsors

Sint Antonius Ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

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

Exclusion criteria

Exclusion criteria: Atrial fibrillation in history Atrial fibrilation diagnosed at ECG hemorragic CVA

Design outcomes

Primary

MeasureTime frame
Fysical complaints of atrial fibrillation (palpitations, short of breath, dizziness, or chest pain) Left atrial enlargement at ECG Left ventricle hypertrophy at ECG Premature atrial complex at ECG (with heartbeats of > 70 bmp) Hyperthyreoidy (TSH 24.0 pmol/l at serum) Ischaemic attacks at several cerebral flow area (detected at CT-scan) Outcome: Atrial fibrillation

Secondary

MeasureTime frame
not applied to

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)