Persistent Atrial Fibrillation Clinical Trial
— NO PERS-AFOfficial title:
Norwegian Randomized Study of Persistent Atrial Fibrillation Treatment: Cryoballoon Versus Radiofrequency Catheter Ablation (NO PERS-AF)
NCT number | NCT03008811 |
Other study ID # | 2016/27 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | November 2016 |
Est. completion date | May 2021 |
Verified date | February 2020 |
Source | Haukeland University Hospital |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This study will compare efficacy and safety of pulmonary vein isolation using a cryoballoon catheter versus a radiofrequency ablation with a contact force sensing catheter for treatment of patients with persistent or longstanding persistent atrial fibrillation.
Status | Completed |
Enrollment | 101 |
Est. completion date | May 2021 |
Est. primary completion date | April 2021 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 75 Years |
Eligibility | Inclusion criteria: - Patients plan to undergo pulmonary vein isolation as the first procedure for symptomatic persistent atrial fibrillation (>7 days) and longstanding persistent atrial fibrillation (> 12 months, but = 3 years) who are refractory to at least one class I or class III antiarrhythmic drug and required at least one electrical or pharmacologic cardioversion. - Subject is at least 18 and = 75 years old. - Subject is able and willing to give informed consent. Exclusion criteria: - Subject has paroxysmal atrial fibrillation (< 7days) or persistent atrial fibrillation with duration > 3 years. - Subject has any previous left atrial ablation procedure or surgery, including pulmonary vein isolation. - Subject has presence of an intracavitary thrombus. - Subject has uncontrolled heart failure. - Subject has severe valvular disease. - Subject has the left atrial diameter > 60 mm confirmed by echocardiography. - Subject has contraindications to systemic anticoagulation with heparin or oral anticoagulants. - Subject has known cryoglobulinaemia. - Subject has severe renal dysfunction. - Subject who is or may potentially be pregnant. - Subject has unstable angina pectoris. - Subject has history of previous myocardial infarction or percutaneous intervention during the last three months. - Subject has chronic obstructive pulmonary disease with detected pulmonary hypertension. |
Country | Name | City | State |
---|---|---|---|
Norway | Haukeland University Hospital | Bergen | |
Norway | University Hospital of North Norway | Tromsø | |
Norway | St Olavs Hospital | Trondheim |
Lead Sponsor | Collaborator |
---|---|
Haukeland University Hospital | St. Olavs Hospital, University Hospital of North Norway |
Norway,
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* Note: There are 18 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | The freedom of any atrial arrhythmias at 12 months. | The primary endpoint is freedom of any atrial arrhythmias at 12 months (at least one episode of atrial fibrillation, or atrial flutter or atrial tachycardia with a duration > 30 seconds documented by 7-day Holter ECG, or any other printed ECG recording). | 12 months | |
Secondary | Procedure duration | Procedure duration documented | 12 months | |
Secondary | Fluoroscopy time | Fluoroscopy time documented | 12 months | |
Secondary | Ablation time | Ablation time documented | 12 months | |
Secondary | Quality of life - Short Form (SF-36) Heath Survey | Short Form (SF-36) Heath Survey filled in by patients. | 12 months. | |
Secondary | Quality of life affected by atrial fibrillation. | The Atrial Fibrillation Effect on Quality-of-life (AFEQT) questionnaire will be filled in by patients. | 12 months. | |
Secondary | Admittance to hospital or emergency services due to symptoms caused by documented atrial arrhythmias. | Hospitalization after the procedre | 12 months. | |
Secondary | The burden of atrial fibrillation | Total duration of atrial fibrillation recorded by 7-day Holter. | 12 months. | |
Secondary | The occurrence of documented left atrial tachycardia and typical or atypical atrial flutter. | Atrial tachycardia or atrial flutter recorded by all types of ECG | 12 months. | |
Secondary | Symptoms related to atrial fibrillation. | Symptoms related to atrial fibrillation documented | 12 months. | |
Secondary | Serious adverse events. | Serious adverse events documented | 12 months. |
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