Antral Lesions Characterization of a New Cryoballoon Ablation System in Terms of Local Impedance Drop

NCT ID: NCT05410379

Last Updated: 2023-09-07

Basic Information

• Recruitment Status: COMPLETED
• Total Enrollment: 30 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2021-09-15
• Study Completion Date: 2023-03-15

Brief Summary

Atrial fibrillation (AF) is defined as a supraventricular tachyarrhythmia with uncoordinated atrial electrical activation and consequently ineffective atrial contraction. Electrocardiographic characteristics of AF include: irregularly irregular R-R intervals (when atrioventricular conduction is not impaired), absence of distinct repeating P waves, and irregular atrial activations.

Different AF classifications have been proposed but, traditionally, four patterns of AF are distinguished, based on presentation, duration, and spontaneous termination of AF episodes. Paroxysmal AF, that terminates spontaneously or with intervention within 7 days of onset. Persistent AF that is continuously sustained beyond 7 days, including episodes terminated by cardioversion (drugs or electrical cardioversion) after >7 days. Long-standing persistent (continuous AF of >12 months' duration) when decided to adopt a rhythm control strategy. Permanent AF, that is accepted by the patient and physician, and no further attempts to restore/maintain sinus rhythm will be undertaken.

The purpose of this study is to perform assessments of local impedance before and after cryoablation performed with the new POLAR X cryoballoon, in order to characterize the quality of the lesion and possibly to associate it with the acute success and 12 months AF recurrence-free rate.

Conditions

Atrial Fibrillation (AF)

Study Design

• Observational Model Type: CASE_ONLY
• Study Time Perspective: PROSPECTIVE

Eligibility Criteria

Inclusion Criteria

1. Subjects indicated for the treatment of AF with the cryoablation system according to current and future Guidelines and system indications for use;

2. Subjects who are willing and capable of providing informed consent;

3. Subjects who are willing and capable of participating in all testing associated with this clinical study at an approved clinical investigational center.

4. Subjects whose age is 18 years or above, or who are of legal age to give informed consent specific to state and national law.

Exclusion Criteria

1. Any known contraindication to an AF ablation or anticoagulation, including those listed in the instructions for use;

2. Subjects with indication for treatment of AF that is not according to current and future Guidelines and system indications for use;

3. Atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or any other reversible or non-cardiac cause;

4. Known or pre-existing severe Pulmonary Vein Stenosis;

5. Evidence of myxoma, LA ( left atrium) thrombus or intracardiac mural thrombus;

6. Previous cardiac surgery (e.g. ventriculotomy or atriotomy, CABG (Coronary artery bypass graft surgery ), PTCA ( Percutaneous transluminal coronary angioplasty), stent procedure) within 90 days prior to enrollment;

7. Implantable cardiac device procedures ,e.g. PM (pacemaker), ICD( implantable cardioverter defibrillators), CRT within 30 days prior to enrollment;

8. Implanted Left Atrial Appendage Closure device prior to the index procedure;

9. Interatrial baffle, closure device, patch, or patent foramen ovale (PFO) occluder;

10. Subjects with severe valvular disease OR with a prosthetic - mechanical or biological

• heart valve (not including valve repair and annular rings);

11. Presence of any pulmonary vein stents;

12. Active systemic infection;

13. Vena cava embolic protection filter devices and/ or known femoral thrombus;

14. Any previous history of cryoglobulinemia;

15. History of blood clotting or bleeding disease;

16. Any prior history of documented cerebral infarct, TIA (transient ischemic attack) or systemic embolism (excluding a post-operative deep vein thrombosis (DVT)) ≤ 180 days prior to enrollment;

17. Subjects who are hemodynamically unstable or with structural heart disease;

18. The subject is unable or not willing to complete follow-up visits and examination for the duration of the study;

19. Life expectancy ≤ 1 year per investigator's opinion;

20. Women of childbearing potential who are, or plan to become, pregnant during the time of the study (method of assessment upon investigator's discretion);

21. Unrecovered/unresolved Adverse Events from any previous invasive Procedure;

22. Subjects who are currently enrolled in another investigational study or registry that would directly interfere with the current study.

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Maria Cecilia Hospital

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

MCH

Cotignola, Ravenna, Italy

Countries

Italy

Other Identifiers

MCH 2021-01

Identifier Type: -

Identifier Source: org_study_id