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Five year outcome of minimally invasive surgical ablation of paroxysmal and persistent atrial fibrillatio

Completed
Conditions
atrial fibrillation
fibrillation
10007521
10007593
Registration Number
NL-OMON42532
Lead Sponsor
Academisch Medisch Centrum
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Completed
Sex
Not specified
Target Recruitment
66
Inclusion Criteria

Patients who have undergone minimal invasive surgical ablation for paroxysmal or persistent atrial fibrillation between 2008 and 2010 in the Academic Medical Center.

Exclusion Criteria

none

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>-Freedom of any recurrence of atrial fibrillation, atrial flutter or atrial<br /><br>tachycardia, documented on ECG or 24-hour Holter within five years after<br /><br>the procedure without the use of antiarrhythmic drugs.<br /><br>-Sinus rhythm on electrocardiogram at follow up visit five years or more ofter<br /><br>the procedure.<br /><br>-Use of antiarrhythmic drugs at follow up visit.</p><br>
Secondary Outcome Measures
NameTimeMethod
<p>-Functional status measured by the SF-36 Quality of Life questionnaire at 60<br /><br>months follow up.<br /><br>-The occurrence of any procedure related complications and the occurrence of<br /><br>other clinical events during 60 months follow up.<br /><br>-Major adverse cardiac events (MACE) during 60 months or more follow up.</p><br>
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