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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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19 February 2015 |
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Main ID: |
NCT01380574 |
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Date of registration:
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16/06/2011 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Safety of Cardioversion of Acute Atrial Fibrillation
FinCV |
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Scientific title:
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Safety of Cardioversion of Acute Atrial Fibrillation |
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Date of first enrolment:
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June 2011 |
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Target sample size:
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7700 |
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Recruitment status: |
Completed |
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URL:
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http://clinicaltrials.gov/show/NCT01380574 |
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Study type:
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Observational |
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Study design:
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Observational Model: Cohort, Time Perspective: Retrospective
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Phase:
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N/A
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Countries of recruitment
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Finland
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Contacts
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Name:
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Juhani Airaksinen, Professor |
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Address:
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Telephone:
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Email:
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Affiliation:
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Turku University Hospital |
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Key inclusion & exclusion criteria
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Inclusion Criteria:
- patients admitted to emergency room because of acute AF in whom electrical or
pharmacological cardioversion was attempted <48 from the beginning of the symptoms
Exclusion Criteria:
- duration of the AF is unknown or >48 hours
Age minimum:
18 Years
Age maximum:
N/A
Gender:
Both
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Health Condition(s) or Problem(s) studied
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Atrial Fibrillation
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Primary Outcome(s)
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Incidence and predictors of thromboembolic complications, especially stroke, and death <31 days after cardioversion of acute AF
[Time Frame: 31 days]
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Secondary Outcome(s)
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Hemodynamic complications of cardioversion
[Time Frame: 31 days]
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Number of therapy non-responder and early recurrence of AF
[Time Frame: 31 days]
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Bleeding complications during the 31 days follow-up
[Time Frame: 31 days]
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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