Atrial Fibrillation Clinical Trial
— FinCV2Official title:
Finnish Elective Cardioversion for Persistent Atrial Fibrillation Study
Verified date | July 2016 |
Source | University of Turku |
Contact | n/a |
Is FDA regulated | No |
Health authority | Finland: National Institute for Health and Welfare |
Study type | Observational |
This is a retrospective multi-center patient cohort study investigating patients with persistent atrial fibrillation (AF) and elective cardioversion (ECV). The aim is to identify clinical predictors for ineffective ECV to improve management quality of persistent AF.
Status | Completed |
Enrollment | 1342 |
Est. completion date | January 2016 |
Est. primary completion date | January 2016 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - All patients with persistent (>48h) atrial fibrillation and elective electrical cardioversion Exclusion Criteria: - Cardioversions for patients with acute (<48h) atrial fibrillation - Pharmacological cardioversions |
Observational Model: Cohort, Time Perspective: Retrospective
Country | Name | City | State |
---|---|---|---|
Finland | Turku University Hospital | Turku |
Lead Sponsor | Collaborator |
---|---|
University of Turku |
Finland,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Fatal or Non-fatal Stroke/TIA | 30 days | Yes | |
Secondary | Arrhythmic Complications | bradyarrhythmias, ventricular tachycardia and ventricular fibrillation | 24 hours | Yes |
Secondary | Failure of Cardioversion | Assessed at discharge | 24 hours | No |
Secondary | Recurrence of AF after ECV | 30 days | No |
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