Repetitive Activation Patterns and Focal Impulses Identification and Ablation in Persistent AF

Persistent Atrial Fibrillation Clinical Trial

— RAPID-AF  

Official title:

Repetitive Activation Patterns and Focal Impulses Identification and Ablation in Persistent AF Using the RHYTHMFINDER-192

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03064451
• Other study ID #: RAPID-AF
• Status: Completed
• Phase: N/A
• Start date: February 22, 2017
• Est. completion date: April 10, 2019

Study information

• Verified date: May 2020
• Source: Biosense Webster, Inc.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The primary purpose of this study is to assess the effectiveness of using CARTOFINDER™ maps created by the RHYTHMFINDER-192 catheter and the CARTOFINDER™ Algorithm to terminate persistent atrial fibrillation (PsAF) to either Normal Sinus Rhythm or Atrial Tachycardia compared to pulmonary vein isolation (PVI) in treating PsAF. The RHYTHMFINDER-192 catheter is investigational, while the CARTOFINDER™ system is CE marked in Europe.

All subjects with persistent AF who are scheduled to undergo a clinically indicated ablation procedure for management of their persistent AF will be the target population for screening. The study will enroll approximately 40-70 subjects. Subjects will undergo CARTOFINDER™ guided ablation (CFGA) followed by PVI. Subjects will have follow-up visits at 7 days, 3, 6 and 12 months postprocedure.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: April 10, 2019
• Est. primary completion date: April 10, 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

1. Age > 18 years.

2. Patients who have signed the Patient Informed Consent Form (ICF)

3. Scheduled to undergo a clinically-indicated catheter ablation procedure for treatment of

1. persistent atrial fibrillation (defined as continuous atrial fibrillation that is sustained beyond seven consecutive days).

2. drug-resistant atrial fibrillation. (failed 1 or more class I or III antiarrhythmic drugs) and demonstrating Persistent AF (requiring drugs or electrical shock to terminate AF)

4. In AF at the time of the baseline CARTOFINDER™ Map (spontaneous)

5. Left Atrium (LA) must demonstrate sufficient electrical activity to allow for the identification of ablation targets.

6. Able and willing to comply with all pre-, post-, and follow-up testing and requirements (e.g. patients not confined by a court ruling)

Exclusion Criteria:

1. Paroxysmal Atrial Fibrillation

2. Continuous AF > 12 months (1-Year) (Longstanding Persistent AF) Subjects previously diagnosed as Long Standing Persistent (LSP) but have demonstrated the ability to maintain Normal Sinus Rhythm for >30 days after cardioversion and have not been in AF greater than 1 year at the time of the procedure remain eligible for inclusion.

3. Previous ablation procedure for PsAF (defined as ablations involving more than only PV isolation)

4. Patients with a left atrial size >55 mm (echocardiography, parasternal long axis view).

5. Inability to restore sinus rhythm for 30 seconds or longer in the opinion of the investigator.

6. Significant congenital anomaly or medical problem that in the opinion of the investigator would preclude enrollment in this study.

7. Atrial arrhythmia patients with structural atrial disease such as a prior history of atriotomy from prior atrial surgery, presence of an atrial septal defect, and/or presence of an atrial septal closure patch.

8. History of or current blood clotting or bleeding abnormalities, contraindication to systemic anticoagulation (i.e., heparin, warfarin, dabigatran, or a direct thrombin inhibitor).

9. significant pulmonary disease, cardiac surgeries, unstable angina, uncontrolled heart failure, acute illness or systemic infection, or any other disease or malfunction that would preclude treatment in the opinion of the investigator.

10. Current enrollment in a study evaluating another device or drug.

11. A complex arrhythmia secondary to electrolyte imbalance, thyroid disease, or reversible or non-cardiac cause.

12. Any cardiac surgery within the past 60 days (2 months) (includes PCI)

13. Subjects that have ever undergone valvular cardiac surgical procedure (i.e., ventriculotomy, atriotomy, and valve repair or replacement and presence of a prosthetic valve)

14. Prior ICD or pacemaker implanted

15. Presence of intramural thrombus, tumor or other abnormality that precludes catheter introduction or manipulation.

16. Presence of a condition that precludes vascular access.

17. Subject has a contra-indication to the device under study per the IFU

18. Women of child bearing potential whom are pregnant, lactating, or planning to become pregnant during the course of the trial.

Related Conditions & MeSH terms

• Atrial Fibrillation
• Persistent Atrial Fibrillation

Intervention

Procedure:
• cartofinder guided ablation followed by PVI
cartofinder guided ablation followed by PVI

Locations

Country	Name	City	State
Belgium	OLV Aalst	Aalst
Belgium	AZ Sint-Jan Brugge	Brugge
Belgium	Universitair Ziekenhuis Antwerpen	Edegem
Canada	Southlake Regional Health Centre	Newmarket	Ontario
Czechia	Nemocnice Ceské Budejovice	Ceské Budejovice
United Kingdom	London Health Sciences Center	London
United Kingdom	St Bartholomew's hospital	London

Sponsors (1)

Lead Sponsor	Collaborator
Biosense Webster, Inc.

Countries where clinical trial is conducted

Belgium,  Canada,  Czechia,  United Kingdom, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Percentage of Participants With Acute Success Post CartoFinder Guided Ablation (CFGA) Only (Before Pulmonary Vein Isolation [PVI] and Without Cardioversion).	Acute success defined as rate of conversion of Atrial Fibrillation to Normal Sinus Rhythm or Atrial Tachycardia, after CARTOFINDER Guided Ablation (CFGA) only (before Pulmonary Vein Isolation [PVI] and without cardioversion).	Up to 7 days
Primary	Percentage of Participants With Acute Success Post CartoFinder Guided Ablation (CFGA) and Pulmonary Vein Isolation (PVI) Without Cardioversion	Acute success defined as rate of conversion of Atrial Fibrillation to Normal Sinus Rhythm or Atrial Tachycardia, after CFGA and PVI without Cardioversion.	Up to 7 days
Primary	Percentage of Participants With Procedural Success	Procedural success defined as the conversion of Atrial Fibrillation to Normal Sinus Rhythm or Atrial Tachycardia after overall ablation procedure, with or without the need for cardioversion.	Up to 7 days
Primary	Percentage of Participants With Recurrence of Atrial Fibrillation, Atrial Flutter, and Atrial Tachycardia Episodes of Greater Than or Equal to (>=) 30 Seconds to Measure the Effectiveness Success Rate for up to 12 Months	Documented AF/AT/AFL recurrence is defined as any occurrence of documented (symptomatic) atrial fibrillation, atrial flutter, and atrial tachycardia episodes >= 30 seconds during the post-blanking period (Day 91-365). Here 'HM' signifies Holter monitoring.	Up to 12 months
Primary	Number of Participants With Early-onset Primary Adverse Events	Incidence of early-onset (within 7 days of the initial mapping and ablation procedure) Primary Adverse Events (PAEs) was reported. PAEs included death, Atria-Esophageal Fistula, Cardiac Tamponade/Perforation, Myocardial Infarction, Stroke/Cerebrovascular Accident, Thromboembolism, Transient Ischemic Attack, Diaphragmatic Paralysis, Pneumothorax, Heart Block, Pulmonary Vein Stenosis, Pulmonary Edema (Respiratory Insufficiency), Pericarditis and Major Vascular Access Complication/Bleeding.	Up to 7 days
Secondary	Number of Participants With Confirmed Entrance Block After Adenosine/Isoproterenol Challenge	Number of participants with confirmed entrance block after adenosine/isoproterenol challenge was reported.	Up to 12 months
Secondary	Change of Intra-cycle Length From Pre-CFGA (Baseline) to Post-CFGA and Post-PVI	Change of intra-cycle length from pre-CFGA to post-CFGA and post-PVI is reported to measure the slowing for the overall Atrial Fibrillation rate in both atrium's.	Pre-CFGA (Baseline) to Post-CFGA and Post-PVI (Up to 7 days)
Secondary	Number of Participants With Serious Adverse Device Effects (SADEs) up to 12 Months	Any serious adverse event which was related to the device and/or the procedure was defined as a SADE.	Up to 12 months
Secondary	Number of Participants With All Serious Adverse Events (SAEs) up to 12 Months	Number of participants with SAEs will be evaluated. An SAE is any AE that results in: death, persistent or significant disability/incapacity, requires inpatient hospitalization or prolongation of existing hospitalization, is life threatening experience, is a congenital anomaly/birth defect, is suspected transmission of any infectious agent via a medicinal product, is medically important, and may jeopardize participant or may require medical or surgical intervention to prevent one of the outcomes listed above.	Up to 12 months
Secondary	Number of Participants With Adverse Device Effects (ADEs) up to 12 Months	Number of participants with adverse device effects was reported. Adverse Device Effect (ADE's) are adverse events related to the use of an investigational medical device. This definition includes adverse events resulting from insufficient or inadequate instructions for use deployment, implantation, installation, or operation, or any malfunction of the investigational medical device. This definition includes any event resulting from use errors or from intentional misuse of the investigational medical device.	Up to 12 months
Secondary	Number of Participants With Procedural Related Serious Adverse Event and Non-serious Adverse Events	An adverse event (AE) is any untoward medical occurrence in a clinical study participant administered a medicinal (investigational or non investigational) product. An AE does not necessarily have a causal relationship with treatment and therefore can be any unfavorable and unintended sign (including an abnormal finding), symptom, or disease temporally associated with use of a medicinal product, whether or not related to that medicinal product. TEAEs were defined as AEs that were reported or worsened on after start of study drug(s) dosing through safety follow-up visit. A serious adverse event (SAE) is any untoward medical occurrence that at any dose resulting in any of following outcomes: results in death, is life-threatening, requires inpatient hospitalization or prolongation of existing hospitalization, results in persistent or significant disability/incapacity, is a congenital anomaly/birth defect, is a suspected transmission of any infectious agent via a medicinal product.	Up to 12 months