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Renal Nerve Denervation After Pulmonary Vein Isolation for Persistent Atrial Fibrillation

Primary Purpose

Atrial Fibrillation

Status

Terminated

Phase

Not Applicable

Locations

Hong Kong

Study Type

Interventional

Intervention

Renal Nerve Denervation

Pulmonary vein isolation

About this trial

This is an interventional treatment trial for Atrial Fibrillation focused on measuring Ablation, Renal Denervation, Cryoballoon

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

Patients age is 18 years or greater;
Patients undergoing a first-time ablation procedure for AF;
Patients with persistent AF;
Persistent AF will be defined as a sustained episode lasting > 7 days and less than 3 years.
Patients with symptomatic AF that is refractory to at least one antiarrhythmic medication;
Symptomatic patients are those who have been aware of their AF at any time within the last 5 years prior to enrollment. Symptoms may include, but are not restricted to, palpitations, shortness of breath, chest pain, fatigue, left ventricular dysfunction, or other symptoms, or any combination of the above.
At least one episode of persistent AF must have been documented by ECG, Holter, loop recorder, telemetry, trans telephonic monitoring (TTM), or implantable device within last 2 years of enrollment in this investigation.

Exclusion Criteria:

Patients with paroxysmal AF;
Paroxysmal AF will be defined as a sustained episode lasting < 7 days.
Patients with long-standing persistent AF;
Long-standing persistent AF will be defined as a sustained episode lasting more than 3 years;
Patients for whom cardioversion or sinus rhythm will never be attempted/pursued;
Patients with AF felt to be secondary to an obvious reversible cause;
Patients with contraindications to systemic anticoagulation with heparin or warfarin or a direct thrombin inhibitor;
Patients with left atrial size ≥ 60 mm (2D echocardiography, parasternal long axis view);
Patients with more than 50% renal artery stenosis identified by duplex ultrasound or renal angiogram;
Patients in whom a renal stent has been in place for less than3 months;
Patients with prior renal artery stent placement, the artery segment beyond the stent margins must be able to accommodate treatments;
Patients with the treatment zone for denervation in the renal artery have areas of atheroma, severe fibromuscular dysplasia, calcification, and aneurysm that cannot be avoided;
Patients with renal dysfunction as demonstrated by an estimated glomerular filtration rate less than 45 mL/min per 1.73 m2 are excluded from both studies;
Pregnant women;
Participation in another interventional study;
Patient with contraindication to left ventricle catheterization by a retrograde aortic approach (eg mechanical aortic valve, severe aortic stenosis and aortic dissection).
Patient with systolic blood pressure <100mmHg.

Sites / Locations

The Chinese University of Hong Kong

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

Pulmonary vein isolation alone

Renal nerve denervation

Arm Description

PVI by cryo-balloon ablation without linear ablation

PVI by cryo-balloon ablation without linear ablation plus bilateral RND using a multi-electrode renal denervation catheter.

Outcomes

Primary Outcome Measures

Freedom from documented AF episodes post PVI by implantable loop recorder by implantable loop recorder.

Freedom from documented AF episodes post PVI as defined by longer than 30 seconds of AF recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication.

Secondary Outcome Measures

Freedom from documented atrial arrhythmia episodes post PVI by implantable loop recorder.

Freedom from documented atrial arrhythmia episodes post PVI as defined by longer than 30 seconds of atrial arrhythmia recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication.

Freedom from symptomatic AF episodes post PVI by implantable loop recorder.

Freedom from symptomatic AF episodes post PVI as defined by longer than 30 seconds of AF recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication.

Freedom from symptomatic atrial arrhythmia episodes post PVI by implantable loop recorder.

Freedom from symptomatic atrial arrhythmia episodes post PVI as defined by longer than 30 seconds of atrial arrhythmia recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication.

Freedom from documented AF episodes post PVI by hand-held smartphone device.

Freedom from documented AF episodes post PVI as defined by 30 seconds of AF recorded by hand-held smartphone device (i.e. Cardiio Rhythm iPhone AF-detection system or AliveCor single-lead ECG device) 2 to 18 months after procedure with or without antiarrhythmic medication.

The mean blood pressure as measured by 24-hour ambulatory blood pressure monitoring.

The mean blood pressure as measured by 24-hour ambulatory blood pressure before and after ablation up to 36 months.

Incidence of peri-procedural complications.

Incidence of peri-procedural complications, including stroke, PV stenosis, cardiac perforation, phrenic nerve palsy, esophageal injury and death.

Procedure duration

Fluoroscopy time during procedure

Number of repeat procedures

Full Information

NCT ID

NCT03246568

First Posted

August 9, 2017

Last Updated

October 18, 2021

Sponsor

Chinese University of Hong Kong

1. Study Identification

Unique Protocol Identification Number

NCT03246568

Brief Title

Renal Nerve Denervation After Pulmonary Vein Isolation for Persistent Atrial Fibrillation

Official Title

Renal Artery Sympathetic Denervation by Catheter Ablation After Pulmonary Vein Isolation for Persistent Atrial Fibrillation

Study Type

Interventional

2. Study Status

Record Verification Date

October 2021

Overall Recruitment Status

Terminated

Why Stopped

no funding to purchase study device

Study Start Date

September 17, 2018 (Actual)

Primary Completion Date

August 31, 2020 (Actual)

Study Completion Date

August 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title

Principal Investigator

Name of the Sponsor

Chinese University of Hong Kong

4. Oversight

Studies a U.S. FDA-regulated Drug Product

Studies a U.S. FDA-regulated Device Product

Data Monitoring Committee

5. Study Description

Brief Summary

Atrial fibrillation (AF) is the most common arrhythmia and it is associated with significant morbidity and mortality. Electrical isolation of the pulmonary vein (PVI) by radiofrequency energy or cryoablation has been shown to be an effective treatment of AF by reducing morbidity, improving quality of life and functional capacity. Renal artery sympathetic denervation (RND) by catheter ablation has been shown in a preliminary study to improve outcome of PVI in patients with paroxysmal and/or persistent AF with concomitant refractory or moderate hypertension. In patients with renal impairment, RND also conferred benefit in reducing AF recurrence after PVI. The initial indication for catheter-based RND is for blood pressure control in patients with resistant hypertension. However, a recent study failed to show significant difference in blood pressure reduction by RND. Therefore, the effect of RND on AF suppression may be independent of blood pressure control. Possible mechanisms of RND on AF may include risk factors modification and anti-arrhythmic effect.

Detailed Description

This prospective randomized study aimed to evaluate the effect of RDN added to PVI for persistent AF. Study will be performed in accordance with Declaration of Helsinki. Study Hypothesis: Catheter based RDN can prevent recurrence of AF in patient with persistent AF undergoing PVI by mechanism not related to hypertension control. Primary outcome measure: Freedom from documented AF episodes post PVI as defined by longer than 30 seconds of AF recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication. Sample Size: This is an exploratory study, the sample size calculation will not be applied and arbitrary assign 20 subjects to each arm will be adopted. Randomization Arms: Patients are randomized in 1:1 fraction to one of the following arms: PVI by cryo-balloon ablation without linear ablation; PVI by cryo-balloon ablation without linear ablation plus bilateral RND using a multi-electrode renal denervation catheter.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study

Atrial Fibrillation

Keywords

Ablation, Renal Denervation, Cryoballoon

7. Study Design

Primary Purpose

Treatment

Study Phase

Not Applicable

Interventional Study Model

Parallel Assignment

Model Description

Research on the Basis of Earlier Theory Renal artery sympathetic denervation (RND) by catheter ablation has been shown in a preliminary study to improve outcome of electrical isolation of the pulmonary vein (PVI) in patients with paroxysmal and/or persistent AF with concomitant refractory hypertension and the same group later showed renal sympathetic denervation improved outcome of PVI in the cohort of paroxysmal and/or persistent AF patients with moderate hypertension. In patients with renal impairment, RND also conferred benefit in reducing AF recurrence after PVI.The initial indication for catheter-based RND is for blood pressure control in patients with resistant hypertension. Early data from clinical trials without sham controls was promising - demonstrating large blood pressure reductions in patients with treatment-resistant hypertension.

Masking

None (Open Label)

Allocation

Randomized

Enrollment

3 (Actual)

8. Arms, Groups, and Interventions

Arm Title

Pulmonary vein isolation alone

Arm Type

Active Comparator

Arm Description

PVI by cryo-balloon ablation without linear ablation

Arm Title

Renal nerve denervation

Arm Type

Experimental

Arm Description

PVI by cryo-balloon ablation without linear ablation plus bilateral RND using a multi-electrode renal denervation catheter.

Intervention Type

Procedure

Intervention Name(s)

Renal Nerve Denervation

Other Intervention Name(s)

Renal artery sympathetic nerve denervation, RND

Intervention Description

Bilateral renal denervation using a multi-polar radiofrequency ablation catheter (Symplicity™ Spyral Cather, Medtronic) in the right and left main, branch, and accessory renal arteries in vessels ranging in diameter between 3 and 8 mm.

Intervention Type

Procedure

Intervention Name(s)

Pulmonary vein isolation

Other Intervention Name(s)

PVI

Intervention Description

PVI by cryo-balloon ablation without linear ablation

Primary Outcome Measure Information:

Title

Freedom from documented AF episodes post PVI by implantable loop recorder by implantable loop recorder.

Description

Freedom from documented AF episodes post PVI as defined by longer than 30 seconds of AF recorded by implantable loop recorder 2 to 18 months after procedure with or without antiarrhythmic medication.

Time Frame