Persistent Atrial Fibrillation Clinical Trial
— CAPAPAF-65Official title:
Cardioversion, Ablation or Pace and Ablate for Persistent Atrial Fibrillation in Over 65s - The CAPAPAF-65 Study
Verified date | September 2018 |
Source | Eastbourne General Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Comparison of (i) catheter ablation, (ii) electrical cardioversion and (iii) pacemaker implantation with AV node ablation for patients over 65 years of age with persistent Atrial Fibrillation.
Status | Completed |
Enrollment | 75 |
Est. completion date | September 2018 |
Est. primary completion date | September 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Patients with symptomatic persistent atrial fibrillation of less than 1-year duration. - Patients must be over 65 years old. - Patients give informed consent prior to participating in this study. Exclusion Criteria: - Paroxysmal atrial fibrillation. - Long-standing persistent or permanent atrial fibrillation. - Previous pacemaker implantation. - Previous atrial ablation. - Patient is unable to take warfarin or other oral anti-coagulant medication. - Patient is suffering with unstable angina in last one week. - Patient has had a myocardial infarction within last two months. - Patient is expecting or has had major cardiac surgery within last two months. - Patient is participating in a conflicting study. - Patient is unable to perform exercise testing. - Patient is mentally incapacitated and cannot consent or comply with follow-up. - Patient has New York Heart Association (NYHA) class III/IV heart failure. - Patient has left ventricular ejection fraction (LVEF) less than 35% not secondary to tachycardia. - Pregnancy. - Patient suffers with other cardiac rhythm disorders. - Recent coronary artery intervention or other factors suggesting clinical instability (ECG, clinical or laboratory findings). |
Country | Name | City | State |
---|---|---|---|
United Kingdom | Eastbourne District General Hospital | Eastbourne | East Sussex |
United Kingdom | Conquest Hospital | St Leonards-on-Sea | East Sussex |
Lead Sponsor | Collaborator |
---|---|
Eastbourne General Hospital |
United Kingdom,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | AF recurrence | Time to recurrence of persistent AF | 12 months | |
Secondary | Patient experience of procedure | Patient experience of each procedure will be assessed by validated questionnaires | Baseline | |
Secondary | Total costs of the treatment options | 12 months | ||
Secondary | AF recurrence >2minutes | Time to recurrence of AF episode > 2 minutes | 12 months | |
Secondary | Symptoms / QOL | To assess differences in symptoms and QOL | 12 months | |
Secondary | Exercise performance | To measure the three treatment effects on VO2 max over time by means of cardiopulmonary exercise testing. | 12 months | |
Secondary | AF burden | To measure the three treatment effects on AF burden | 12 months | |
Secondary | Sleep apnoea | To assess the impact of the three treatment options on sleep apnoea scores | 6 months |
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