GENESIS Feasibility Study of the BARD Over-the-Wire Mesh Ablation System for the Treatment of Paroxysmal Atrial Fibrillation

NCT ID: NCT01430949

Last Updated: 2013-09-30

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 42 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-11-30
• Study Completion Date: 2013-08-31

Brief Summary

The Genesis Feasibility Study will collect clinical information on the use of the Bard Over-the-Wire Mesh Ablation System to access and perform electrophysiological mapping, cardiac stimulation and radiofrequency ablation in the region of the pulmonary vein (PV) ostia for the treatment of patients with Paroxysmal Atrial Fibrillation. Patients will be followed up for 12 months to assess the primary safety endpoint of Major Complications (a composite safety endpoint)and effectiveness, defined as Long-Term Success (freedom from recurrent atrial arrhythmia.

Detailed Description

Atrial fibrillation (AF) is the most common sustained arrhythmia seen by the physician. Its prevalence in the population increases with age, and it is estimated to affect over 4% of the population above the age of 60. Common approaches to AF management includes the use of anti-arrhythmic drugs to control the arrhythmia.

An alternative to treatment of AF using drug therapy is ablation of cardiac tissue, with the goal of disrupting the aberrant electrical pathways that cause AF through the creation of ablation lesions within the left atrium. There are several different approaches to creating lesions to treat AF, although both substrate derived and focal AF mechanisms share a common ablation therapy protocol in which the PVs are isolated by a series of ablation lines placed endocardially, either around the PV ostia or more proximally from the PV ostia at the atrial carinae.

The Over-the-Wire Mesh Ablation System (OTW MAS) catheter is a combined mapping and ablation catheter designed to create lesions at the PV ostium. The Genesis Feasibility Study is designed to collect clinical information on the use of the OTW MAS to access and perform electrophysiological mapping, cardiac stimulation and radiofrequency ablation in the region of the pulmonary vein (PV) ostia for the treatment of patients with Paroxysmal Atrial Fibrillation (PAF).

Conditions

Paroxysmal Atrial Fibrillation

Keywords

Paroxysmal Atrial Fibrillation; Catheter Ablation; Pulmonary Vein Isolation; Radio Frequency Ablation

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Over-the-Wire Mesh Ablation System

Group Type: EXPERIMENTAL

Catheter Ablation of Paroxysmal Atrial Fibrillation

Intervention Type: PROCEDURE

Catheter ablation for the treatment of paroxysmal atrial fibrillation. A pulmonary vein isolation procedure will be performed using the OTW MAS and radiofrequency ablation.

Interventions

Catheter Ablation of Paroxysmal Atrial Fibrillation

Catheter ablation for the treatment of paroxysmal atrial fibrillation. A pulmonary vein isolation procedure will be performed using the OTW MAS and radiofrequency ablation.

Intervention Type: PROCEDURE

Other Intervention Names

GENESIS; BEP-4409; Bard Over-the-Wire Mesh Ablation System; OTW MAS; Paroxysmal Atrial Fibrillation; PAF; Feasibility

Eligibility Criteria

Inclusion Criteria

• Symptomatic PAF refractory to at least one Class I-IV antiarrhythmic drug.
• Minimum one documented PAF episode >30 sec duration within prior 12 months.
• Minimum three PAF episodes during prior 12 months.
• 18 years or older.

Exclusion Criteria

• AF due to reversible causes.
• More than 2 cardioversions during the 6 months
• Previous surgical or catheter based ablation of the LA to treat AF.
• Permanent or persistent AF.
• Requirement for ablation lesions other than those defined in protocol
• LA > 50 mm in major dimension(measured by TTE).
• Any single PV > 25 mm in major diameter and/or presence of common os not suitable for ablation
• Ejection fraction <35%.
• Patent foramen ovale (PFO)or atrial septal defect (ASD)
• Cardiac myopathy (e.g., HOCM, cardiac sarcoidosis).
• Myocardial infarction in previous 2 months screening.
• Currently unstable angina.
• Any cardiac surgery in previous 3 months prior to screening.
• Implantable device capable of recording cardiac rhythm, (e.g ICD, pacemaker or implantable loop recorder.
• Clinically significant valvular heart disease or a replacement heart valve.
• Congestive heart failure (NYHA classification III or IV).
• Renal dialysis or creatinine > 2.0 mg/dl.
• Contraindication to anti-coagulation therapy (e.g., warfarin, heparin).
• Contraindication to transseptal procedure.
• Any cerebral ischemic event, including TIA in the 6 months prior to screening.
• Any known uncontrolled bleeding or thrombotic disorder.
• Women who are known to be pregnant or nursing.
• Uncontrolled hyperthyroidism.
• Patients currently enrolled in any other study during the 30 days prior to screening.
• Any other significant uncontrolled or unstable medical condition (e.g., active systemic infection).
• A life expectancy of less than one year.
• Currently documented intracardiac thrombus.

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

Sponsors

C. R. Bard

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

David Ciavarella, MD

Role: STUDY_CHAIR

CR Bard Inc

Locations

University Hospital

London, Ontario, Canada

Southlake Regional Health Centre

Newmarket, Ontario, Canada

Herz-und Gefässzentrum Bad Bevensen

Bad Bevensen, , Germany

Deutsches Herzzentrum Berlin (DHZB)

Berlin, , Germany

Herzzentrum Mūnchen

Munich, , Germany

The Heart Hospital

London, , United Kingdom

Countries

Canada; Germany; United Kingdom

Other Identifiers

BEP-4409-2010

Identifier Type: -

Identifier Source: org_study_id