Prospective Evaluation of Open Irrigated Ablation Catheters With High Resolution Mapping to Treat Paroxysmal Atrial Fibrillation

Boston Scientific Corporation415 enrolled

Overview

To obtain data for the Rhythmia™ Mapping System in conjunction with Boston Scientific Open-Irrigated (OI) Catheters for ablation of Paroxysmal Atrial Fibrillation (PAF) according to current international and local guidelines. Primary objective: To assess acute and long-term outcomes for the Rhythmia Mapping System in conjunction with Boston Scientific Open-Irrigated Ablation Catheters to treat de novo Paroxysmal Atrial Fibrillation. De Novo PAF is defined as subjects undergoing first ablation procedure for PAF with no prior left atrial ablation (RF, Cryo, Surgical).

STUDY OBJECTIVE(S) -- To obtain data for the Rhythmia™ Mapping System in conjunction with Boston Scientific Open-Irrigated (OI) Catheters for ablation of Paroxysmal Atrial Fibrillation (PAF) according to current international and local guidelines. PRIMARY OBJECTIVE -- To assess acute and long-term outcomes for the Rhythmia Mapping System in conjunction with Boston Scientific Open-Irrigated Ablation Catheters to treat de novo Paroxysmal Atrial Fibrillation. De Novo PAF is defined as subjects undergoing first ablation procedure for PAF with no prior left atrial ablation (RF, Cryo, Surgical). INDICATION(S) FOR USE -- Study devices will be used per approved Indications for Use for each geography. DEVICES / SYSTEM USED IN THE STUDY -- The study will include the following Boston Scientific Open-Irrigated Catheters in geographies where commercially approved for PAF ablation: * Blazer Open-Irrigated Ablation Catheter * IntellaNav Open-Irrigated Ablation Catheter * IntellaNav MiFi Open-Irrigated Ablation Catheter * IntellaTip MiFi Open-Irrigated Ablation Catheter * Rhythmia Mapping System Gen 1or Rhythmia HDx, equipped with Software 1.4 or any successive commercially approved versions. * IntellaMap Orion Catheter CONTROL DEVICE -- There are no control devices in this study STUDY DESIGN -- Prospective, non-randomized, multicenter (global), post approval clinical study (PAS). All subjects fitting the enrollment criteria, signing the consent and undergoing the index procedure with the study devices will be followed up for three years to complete the PAS design mandated from the FDA to collect post-market data for Boston Scientific Open-Irrigated Catheters and will be followed for three years. PLANNED NUMBER OF SUBJECTS -- The study will enroll 415 subjects. PLANNED NUMBER OF SITES / COUNTRIES -- The study is global (US, EU, Asia-Pacific) with 25-50 centers. A minimum of 50% of the sites will be selected from the US. No study site will be allowed to contribute more than 41 subjects (10% of the 415 enrollments requirement). FOLLOW-UP SCHEDULE -- Study Follow-ups are at: pre-discharge, 1 month (phone check), 3 months (blanking period), 6 months (phone check), 12 months, 24 months and 36 months. STUDY DURATION -- Study is expected to be completed in approximately five years (12-24 month enrollment period with three year follow-up). PARTICIPANT DURATION -- The study duration for each subject is expected to be approximately three years.

Eligibility

Sex: ALLMin age: 20 Years

Medical Language ↔ Plain English

Inclusion Criteria: 1. History of recurrent symptomatic Paroxysmal Atrial Fibrillation, defined as AFib that terminates spontaneously or with intervention within seven days of onset. Minimum documentation includes a physician's note indicating recurrent self-terminating Atrial Fibrillation AND one electrocardiographically documented AF episode within 6 months prior to enrollment. 2. Subjects who are eligible for an ablation procedure for Paroxysmal Atrial Fibrillation with the Rhythmia Mapping system according to current international and local guidelines 3. Subjects who are eligible for an ablation procedure for Paroxysmal Atrial Fibrillation with a Boston Scientific Open-Irrigated Ablation Catheter according to current international and local guidelines 4. Subjects who are willing and capable of providing informed consent 5. Subjects who are willing and capable of participating in all testing associated with this clinical investigation at an approved clinical investigational center 6. Subjects whose age is 20 years or above, or who are of legal age to give informed consent specific to state and national law. Exclusion Criteria: 1. Subjects enrolled in any other concurrent clinical study, with the exception of local mandatory governmental registries and observational studies/registries, without the written approval from Boston Scientific 2. Subjects unable or unwilling to complete follow-up visits and examination for the duration of the study 3. Subjects who have undergone any previous left atrial cardiac ablation (RF, Cryo, surgical) 4. Subjects who have undergone any cardiac ablation within 30 days prior to enrollment 5. Unrecovered/unresolved Adverse Events from any previous invasive procedure 6. Life expectancy \<= three years per physician opinion 7. Women of childbearing potential who are, or plan to become, pregnant during the time of the study (method of assessment upon physician's discretion) 8. Known cardiac thrombus within 60 days prior to enrollment 9. History of CVA, TIA or PE within 90 days prior to enrollment 10. Implanted pacemaker, ICD, or CRT leads within 90 days prior to enrollment 11. Implanted Left atrial appendage closure device prior to the index procedure 12. Prosthetic mitral or tricuspid heart valves (subjects with successful mitral valve repair allowed- annular ring constitutes repair) 13. Left atrial diameter greater than 5.5cm 14. Documented or suspected stenosis of any pulmonary veins. 15. Atrial fibrillation secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause. 16. Contraindication for anticoagulation 17. Clinically significant mitral valve regurgitation or stenosis per investigator discretion. 18. Any cardiac surgery ≤ 90 days from consent date. 19. Any electrocardiographically documented episode of Persistent AFib, defined as AFib lasting longer than 7 days from onset.

Locations (26)

University of Alabama at Birmingham

Birmingham, Alabama, United States

Torrance Memorial Medical Center

Torrance, California, United States

Broward General Medical Center

Miami, Florida, United States

AdventHealth Orlando

Orlando, Florida, United States

St. Lukes Idaho Cardiology Associates

Boise, Idaho, United States

University of Chicago Hospital

Chicago, Illinois, United States

St. John's Hospital

Springfield, Illinois, United States

University of Iowa Hospitals and Clinics

Iowa City, Iowa, United States

Nebraska Heart Institute

Lincoln, Nebraska, United States

Dartmouth Hitchcock Medical Center

Lebanon, New Hampshire, United States

...and 16 more locations

Outcomes

Primary Outcomes

Number of Participants Safety Event-free at 12 Months Post Procedure

This measure reports the observed safety event -free rate at 12 Months follow up. The safety events are a composite of acute primary safety events (events occurring within seven days post-procedure or hospital discharge, whichever is later), and chronic primary safety events (events occurring through 3- or 12-months post-procedure, as listed below). Acute primary safety endpoint events are defined as the following: * Death * Myocardial infarction (MI) * Vagal Nerve Injury/Gastroparesis * Transient ischemic attack (TIA) * Stroke/Cerebrovascular accident (CVA) * Thromboembolism * Pericarditis * Cardiac tamponade/perforation * Pneumothorax * Vascular access complications * Pulmonary edema/heart failure * AV block Chronic primary safety endpoint events are defined as the following occurring through: 3 Months post-procedure 12 Months post-procedure * Atrial esophageal fistula * Pericardial effusion * Pulmonary vein stenosis (symptomatic and requiring intervention)

Time frame: 12 months

Number of Participants Effectiveness Event -Free at 12 Months Post Procedure

The primary effectiveness endpoint is defined as the event-free rate at 12 months post-procedure. Primary effectiveness events are defined as: * Acute procedural failure * More than one repeat procedure during the blanking period (90 days post index procedure) * Documented atrial fibrillation, or new onset of atrial flutter or atrial tachycardia event (≥ 30 seconds in duration from an event monitor or Holter, or from a 10 second 12-lead EKG) between 91 days and 365 days post index procedure * Any of the following interventions for atrial fibrillation, or new onset of atrial flutter or atrial tachycardia between 91 days and 365 days post index procedure: * Repeat procedure * Cardioversion * Prescribed any AAD\* * AADs for endpoint will consist of all Class I/III and any Class II/IV medications taken for control of AF/AT/AFL recurrence

Time frame: 12 Months

Secondary Outcomes

Number of Participants Event Free Rate (Secondary)

The secondary effectiveness endpoint is defined as the event-free at 12 months post-procedure. Secondary effectiveness events are defined as: * Acute procedural failure * More than one repeat procedure during the blanking period (90 days post index procedure) * Documented symptomatic atrial fibrillation, or new onset of atrial flutter or atrial tachycardia event (≥ 30 seconds in duration from an event monitor or Holter, or from a 10 second 12-lead EKG) between 91 days and 365 days post index procedure * Any of the following interventions for atrial fibrillation, or new onset of atrial flutter or atrial tachycardia between 91 days and 365 days post index procedure: * Repeat procedure * Cardioversion * Prescribed a higher dose of any AAD\* documented at baseline * Prescribed a new AAD\* not documented at baseline * AADs for endpoint will consist of all Class I/III and any Class II/IV medications taken for control of AF/AT/AFL recurrence