Waveform Periodicity Analysis of Complex Fractionated Electrograms in Patients With Persistent Atrial Fibrillation

NCT05333952 | Unknown

• 1 other identifier: 2018-07-008C
• Study Type: interventional
• Target: 80
• Locations: 1 country
• Sites: 1

Brief Summary

Atrial fibrillation (AF) has been the most frequently occurring, sustained arrhythmia, which causes significant morbidity and mortality. AF may not always be a totally random process. It can be maintained by stable and rapid reentrant circuits resulting in fibrillary conduction throughout the atria. During mapping of AF, difficulty is frequently encountered during the identification of culprit sites and an analysis of the wave propagation particularly when the electrogram signals demonstrate wide temporal and spatial disparities. Catheter ablation targeting regions with fractionated potentials or high frequencies during AF, has been previously proposed as a treatment strategy. However, the benefit of adjunctive CFAE (complex fractionated atrial electrogram) ablation or linear ablation after successful PVI (pulmonary vein isolation) was controversial based on the recent data from the Substrate and Trigger Ablation for Reduction of Atrial Fibrillation Trial Part II (STAR AF II) trial. Therefore, the optimal ablation strategy for persistent AF remains undetermined and an alternative approach has to be explored.

Conditions

Atrial Fibrillation, Persistent

Keywords

Catheter ablation; Mapping technique; Substrate mapping; Non-linear electrogram morphology analysis

Outcome Measures

Primary Outcomes (1)

• changes in retention rate of normal sinus rhythm after catheter-based ablation of atrial fibrillation

  A 24-hour Holter monitoring and/or ECG (7 days recordings) will be performed at 3, 6, 9, and 12 months post ablation and/or when the patients experience symptoms suggestive of a tachycardia after the ablation. Measurements: documentation of AF signal duration more than 30 seconds.

  Baseline and 3, 6, 9 and 12 months after catheter-based ablation of atrial fibrillation

Secondary Outcomes (3)

• LAD

  after catheter ablation of atrial fibrillation 3, 6, 12 month

• LVEF

  after catheter ablation of atrial fibrillation 3, 6, 12 month

• e/e'

  after catheter ablation of atrial fibrillation 3, 6, 12 month

Study Arms (2)

Pulmonary vein isolation + Waveform Periodicity Group

EXPERIMENTAL

Pulmonary vein isolation + Substrate ablation

Procedure: Pulmonary vein isolation; Procedure: Substrate ablation(PRISM based)

Pulmonary vein isolation group

OTHER

Pulmonary vein isolation (Conventional treatment)

Procedure: Pulmonary vein isolation

Interventions

Pulmonary vein isolation PROCEDURE

The 3D geometry of the LA will be created using CARTO 3 system (version 6) with UDM Module and VISITAG Optimum Device Performance (ODP) module. Continuous circumferential lesions will then be created encircling the right and left PV ostia using a 7.5F, 3.5-mm Thermocool SMARTTOUCH ablation catheter (Biosense Webster, Inc., Diamond Bar, CA, USA).Pentaray catheter will be used and facilitate the high density mapping of atrial substrate (PentarayTM, Biosense Webster Inc., Diamond Bar, CA, USA). The radiofrequency energy will be applied with contact force range 5-25 g continuously with a target Ablation Index target 380-400 on the posterior wall and 550 - 600 on the anterior wall and maximum power of 25-35W in a power control mode.

Pulmonary vein isolation + Waveform Periodicity Group; Pulmonary vein isolation group

Substrate ablation(PRISM based) PROCEDURE

Substrate modification will be guided by waveform periodicity analysis. The User Defined Map of waveform periodicity analysis will be also created by CARTO 3 system (version 6) with and VISITAG ODP module. Pentaray catheter will be used and facilitate the high density mapping of atrial substrate (PentarayTM, Biosense Webster Inc., Diamond Bar, CA, USA). Substrate modification based on waveform periodicity analysis will be performed by using a 7.5F, 3.5-mm Thermocool SMARTTOUCH ablation catheter (Biosense Webster, Inc., Diamond Bar, CA, USA). The radiofrequency energy will be applied with contact force range 5-25 g continuously with a target Ablation Index target 380-400 on the posterior wall and 550 - 600 on the anterior wall and maximum power of 25-35W in a power control mode.

Pulmonary vein isolation + Waveform Periodicity Group

Eligibility Criteria

• Age: 20 Years - 90 Years
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Patents who sign the informed consent forms, and allow to be followed.
• Symptomatic AF refractory or intolerant to at least one Class 1 or 3 antiarrhythmic medication.
• Patients with persistent/permanent AF (sustained beyond seven days, or lasting less than seven days but necessitating pharmacologic or electrical cardioversion).
• Patients with age equal or greater than 20 years old regardless of gender.

You may not qualify if:

• The presence of a atrial or ventricular thrombus.
• Patients who are allergic to or unsuitable for use with the contrast media.
• Pregnant patients or patients who are unavailable to receive X-ray.
• Patients with renal insufficiency.
• Patients had autonomic nervous system disorder (e.g. respiratory apnea) or previous catheter ablation in the LA or MAZE procedure.
• Patients who do not need atrial substrate modification (patients with non-paroxysmal AF respond to PVI in terms of procedural termination of AF).
• Patients with age less than 20 years old or greater than 90 years old regardless of gender.

Sponsors & Collaborators

• Taipei Veterans General Hospital, Taiwan: lead

Study Sites (1)

Taipei General Veterans Hospital

Taipei, 112, Taiwan

RECRUITING

Related Publications (4)

• Lin CY, Lin YJ, Lo MT, Chiang CH, Chen YY, Kuo L, Chang SL, Lo LW, Hu YF, Chao TF, Chung FP, Liao JN, Chang TY, Lin C, Tuan TC, Wu CI, Liu CM, Liu SH, Cheng WH, Lugtu IC, Jain A, Ton AN, Hermanto DY, Chen SA. Efficacy of Patient-Specific Strategy: Catheter Ablation Strategy of Persistent Atrial Fibrillation Based on Morphological Repetitiveness by Periodicity and Similarity. Circ Arrhythm Electrophysiol. 2021 May;14(5):e009719. doi: 10.1161/CIRCEP.121.009719. Epub 2021 May 17. No abstract available.

  PMID: 33998256 RESULT

• Hsieh YC, Lin YJ, Lo MT, Chen YY, Lin CY, Lin C, Chung FP, Lo LW, Chang SL, Chao TF, Hu YF, Tuan TC, Liao JN, Wu CI, Liu CM, Vicera JB, Chen CC, Chin CG, Lugtu IC, Chen SA. Optimal substrate modification strategies using catheter ablation in patients with persistent atrial fibrillation: 3-year follow-up outcomes. J Cardiovasc Electrophysiol. 2021 Jun;32(6):1561-1571. doi: 10.1111/jce.15033. Epub 2021 May 5.

  PMID: 33825268 RESULT

• Lin CY, Lin YJ, Narayan SM, Baykaner T, Lo MT, Chung FP, Chen YY, Chang SL, Lo LW, Hu YF, Liao JN, Tuan TC, Chao TF, Te ALD, Kuo L, Vicera JJB, Chang TY, Salim S, Chien KL, Chen SA. Comparison of phase mapping and electrogram-based driver mapping for catheter ablation in atrial fibrillation. Pacing Clin Electrophysiol. 2019 Feb;42(2):216-223. doi: 10.1111/pace.13573. Epub 2018 Dec 27.

  PMID: 30536679 RESULT

• Lin CY, Lin YJ, Higa S, Tsai WC, Lo MT, Chiang CH, Chang SL, Lo LW, Hu YF, Chao TF, Chung FP, Liao JN, Chang TY, Lin C, Tuan TC, Kuo L, Wu CI, Liu CM, Liu SH, Kuo MJ, Liao YC, Chuang CM, Chen YY, Hsieh YC, Chen SA. Catheter Ablation With Morphologic Repetitiveness Mapping for Persistent Atrial Fibrillation. JAMA Netw Open. 2023 Nov 1;6(11):e2344535. doi: 10.1001/jamanetworkopen.2023.44535.

  PMID: 37991761 DERIVED

MeSH Terms

Conditions

Atrial Fibrillation

Condition Hierarchy (Ancestors)

Arrhythmias, Cardiac; Heart Diseases; Cardiovascular Diseases; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Officials

• Yenn-Jiang Lin, MD, PhD

  Director of Cardiology Division of Taipei Veterans General Hospital

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Chia-Hsin Chiang

CONTACT

+886-2-28712121; qqsnoopy0223@gmail.com

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: PARALLEL
• Sponsor Type: OTHER GOV
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 1, 2022
• First Posted: April 19, 2022
• Study Start: February 19, 2019
• Primary Completion: December 31, 2022
• Study Completion: December 31, 2025
• Last Updated: June 6, 2022

Record last verified: 2022-06

Data Sharing

• IPD Sharing: Will not share

Locations

TW (1)