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Efficacy Rate of Unipolar Polarity Switch for Lesion Assessment in Pulmonary Vein Isolation

Primary Purpose

Atrial Fibrillation

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Unipolar Polarity Switch Left
Unipolar Polarity Switch Right
Sponsored by
Kansas City Heart Rhythm Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Atrial Fibrillation

Eligibility Criteria

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

Inclusion Criteria:

  • All Patients ≥ 18 years of age
  • Undergoing pulmonary vein isolation for De-Novo Atrial Fibrillation.

Exclusion Criteria:

  • Patients unable to give consent
  • Who do not have De-novo AF.

Sites / Locations

  • Kansas City Heart Rhythm InstituteRecruiting
  • Overland Park Regional Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Unipolar Polarity Switch Left and CAI-OPR-LAAP Right

CAI-OPR-LAAP Left and Unipolar Polarity Switch Right

Arm Description

Outcomes

Primary Outcome Measures

Efficacy rate of loss of unipolar negative component
Observe the efficacy rate of loss of unipolar negative component in isolation of the Pulmonary Veins. Loss of unipolar negative component will be assessed during the Radiofrequency ablation procedure. The durability of Pulmonary vein isolation will be assessed at 12 month follow up, if there is recurrence of Atrial fibrillation.
Number of patients with Esophageal Injury
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Esophageal Injury
Number of patients with TIA/CVA
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - transient ischemic attack/Cerebrovascular accident (TIA/CVA)
Number of patients with Bleeding/Hematoma
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Bleeding/Hematoma
Number of patients with Pericardial Effusion
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Pericardial Effusion
Number of patients with need for open heart surgery
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - need for open heart surgery
Number of patients with phrenic nerve injury
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - phrenic nerve injury
Number of patients with pulmonary vein stenosis
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - pulmonary vein stenosis
Esophageal Temp max (existing protocol)
Esophageal temp max (existing protocol)
Esophageal "Time above threshold"
Esophageal "Time above threshold"
Esophageal "Time to return to baseline"
Esophageal "Time to return to baseline"
Images comparing PURE EP unipolar signals against Claris unipolar signals
Observe if the quality of PURE EP's unipolar signals are acutely and better suited for lesion assessment? This outcome compares mapping images with site of activation to the PURE EP electrogram and compare if they correspond to each other.

Secondary Outcome Measures

Compare 1st pass isolation
Compare 1st pass isolation in the Unipolar polarity switch group to Carto's Ablation Index per Overland Park Regional's Left Atrial Ablation Protocol (CAI-OPR-LAAP)
Total RF Time
Total RF Time in pulmonary veins with Unipolar polarity switch as endpoint vs. CAI-OPR-LAAP
Discrimination with High Frequency Algorithm as a confirmation tool
In Left Superior Vein, Right Superior Vein, and Right Inferior Vein, validate Near Field and Far Field Discrimination with High Frequency Algorithm as a confirmation tool (Visitag #'s annotated into PURE EP)
6-month freedom from AF
6-month freedom from AF
Redo's within 1 year
Redo's within 1 year which vein randomized group reconnected
Location of Catheter tip
Location of Catheter tip (LSPV, RSPV, RIPV, LIPV, LAA, Other) (carto image)
Duration of HFA channel compared to Bipolar
Duration of HFA channel compared to Bipolar, Was there both a near and far field component?

Full Information

First Posted
July 6, 2022
Last Updated
October 17, 2023
Sponsor
Kansas City Heart Rhythm Research Foundation
Collaborators
Kansas City Heart Rhythm Institute, Overland Park, KS
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1. Study Identification

Unique Protocol Identification Number
NCT05464537
Brief Title
Efficacy Rate of Unipolar Polarity Switch for Lesion Assessment in Pulmonary Vein Isolation
Official Title
To Assess the Efficacy Rate of Unipolar Polarity Switch for Lesion Assessment in Pulmonary Vein Isolation
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 28, 2023 (Actual)
Primary Completion Date
December 2024 (Anticipated)
Study Completion Date
December 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Kansas City Heart Rhythm Research Foundation
Collaborators
Kansas City Heart Rhythm Institute, Overland Park, KS

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The technique of intraprocedural electrogram morphology as a measure of lesion effectiveness in an attempt to achieve durable PVI, clearly led to shortened procedural time, radiation exposure, and superiority in outcomes, with the implementation of a reproducible, readily available intraprocedural tool that can be applied universally.
Detailed Description
One initial study reported that unipolar atrial EGM modification was a useful end point for RF energy delivery. They compared 2 groups of patients with paroxysmal AF undergoing PVI facilitated by an electroanatomic mapping system, merged preprocedural LA computed tomographic scan, and a circular mapping catheter. They were the first to use intraprocedural electrogram morphology as a measure of lesion effectiveness in an attempt to achieve durable PVI. The technique, clearly led to shortened procedural time, radiation exposure, and superiority in outcomes, with the implementation of a reproducible, readily available intraprocedural tool that can be applied universally. As there is scant data is this area with lack of randomized human trials, planned on building and further validating evidence from Bortone et al in demonstrating that loss of unipolar negative component during PVI can serve a great adjuvant tool for achieving durability of PVI with overall lesser procedural time and no significant increase in adverse events.

6. Conditions and Keywords

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

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Unipolar Polarity Switch Left and CAI-OPR-LAAP Right
Arm Type
Active Comparator
Arm Title
CAI-OPR-LAAP Left and Unipolar Polarity Switch Right
Arm Type
Active Comparator
Intervention Type
Other
Intervention Name(s)
Unipolar Polarity Switch Left
Intervention Description
10-15 Left veins are randomized to Unipolar Polarity Shift, right veins are randomized to CAI-OPR-LAAP
Intervention Type
Other
Intervention Name(s)
Unipolar Polarity Switch Right
Intervention Description
10-15 cases randomized to CAI-OPR-LAAP on left veins, and Unipolar Polarity Switch on right veins
Primary Outcome Measure Information:
Title
Efficacy rate of loss of unipolar negative component
Description
Observe the efficacy rate of loss of unipolar negative component in isolation of the Pulmonary Veins. Loss of unipolar negative component will be assessed during the Radiofrequency ablation procedure. The durability of Pulmonary vein isolation will be assessed at 12 month follow up, if there is recurrence of Atrial fibrillation.
Time Frame
Procedure day and 12 month follow-up day
Title
Number of patients with Esophageal Injury
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Esophageal Injury
Time Frame
1 year
Title
Number of patients with TIA/CVA
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - transient ischemic attack/Cerebrovascular accident (TIA/CVA)
Time Frame
1 year
Title
Number of patients with Bleeding/Hematoma
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Bleeding/Hematoma
Time Frame
1 year
Title
Number of patients with Pericardial Effusion
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - Pericardial Effusion
Time Frame
1 year
Title
Number of patients with need for open heart surgery
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - need for open heart surgery
Time Frame
1 year
Title
Number of patients with phrenic nerve injury
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - phrenic nerve injury
Time Frame
1 year
Title
Number of patients with pulmonary vein stenosis
Description
Number of patients with intraprocedural and post procedure adverse events and serious adverse events - pulmonary vein stenosis
Time Frame
1 year
Title
Esophageal Temp max (existing protocol)
Description
Esophageal temp max (existing protocol)
Time Frame
1 day
Title
Esophageal "Time above threshold"
Description
Esophageal "Time above threshold"
Time Frame
1 day
Title
Esophageal "Time to return to baseline"
Description
Esophageal "Time to return to baseline"
Time Frame
1 day
Title
Images comparing PURE EP unipolar signals against Claris unipolar signals
Description
Observe if the quality of PURE EP's unipolar signals are acutely and better suited for lesion assessment? This outcome compares mapping images with site of activation to the PURE EP electrogram and compare if they correspond to each other.
Time Frame
1 day
Secondary Outcome Measure Information:
Title
Compare 1st pass isolation
Description
Compare 1st pass isolation in the Unipolar polarity switch group to Carto's Ablation Index per Overland Park Regional's Left Atrial Ablation Protocol (CAI-OPR-LAAP)
Time Frame
1 day
Title
Total RF Time
Description
Total RF Time in pulmonary veins with Unipolar polarity switch as endpoint vs. CAI-OPR-LAAP
Time Frame
1 day
Title
Discrimination with High Frequency Algorithm as a confirmation tool
Description
In Left Superior Vein, Right Superior Vein, and Right Inferior Vein, validate Near Field and Far Field Discrimination with High Frequency Algorithm as a confirmation tool (Visitag #'s annotated into PURE EP)
Time Frame
1 day
Title
6-month freedom from AF
Description
6-month freedom from AF
Time Frame
6 months
Title
Redo's within 1 year
Description
Redo's within 1 year which vein randomized group reconnected
Time Frame
1 year
Title
Location of Catheter tip
Description
Location of Catheter tip (LSPV, RSPV, RIPV, LIPV, LAA, Other) (carto image)
Time Frame
1 day
Title
Duration of HFA channel compared to Bipolar
Description
Duration of HFA channel compared to Bipolar, Was there both a near and far field component?
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All Patients ≥ 18 years of age Undergoing pulmonary vein isolation for De-Novo Atrial Fibrillation. Exclusion Criteria: Patients unable to give consent Who do not have De-novo AF.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Donita Atkins
Phone
816-651-1969
Email
datkins@kchrf.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Dhanunjaya Lakkireddy
Organizational Affiliation
Kansas City Heart Rhythm Institute
Official's Role
Principal Investigator
Facility Information:
Facility Name
Kansas City Heart Rhythm Institute
City
Overland Park
State/Province
Kansas
ZIP/Postal Code
66211
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Donita Atkins
Facility Name
Overland Park Regional Medical Center
City
Overland Park
State/Province
Kansas
ZIP/Postal Code
66215
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Donita Atkins

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
26092576
Citation
Bortone A, Brault-Noble G, Appetiti A, Marijon E. Elimination of the negative component of the unipolar atrial electrogram as an in vivo marker of transmural lesion creation: acute study in canines. Circ Arrhythm Electrophysiol. 2015 Aug;8(4):905-11. doi: 10.1161/CIRCEP.115.002894. Epub 2015 Jun 19.
Results Reference
background
PubMed Identifier
31164003
Citation
Pambrun T, Durand C, Constantin M, Masse A, Marra C, Meillet V, Haissaguerre M, Jais P, Bortone A. High-Power (40-50 W) Radiofrequency Ablation Guided by Unipolar Signal Modification for Pulmonary Vein Isolation: Experimental Findings and Clinical Results. Circ Arrhythm Electrophysiol. 2019 Jun;12(6):e007304. doi: 10.1161/CIRCEP.119.007304. Epub 2019 Jun 5.
Results Reference
background
PubMed Identifier
24097371
Citation
Bortone A, Appetiti A, Bouzeman A, Maupas E, Ciobotaru V, Boulenc JM, Pujadas-Berthault P, Rioux P. Unipolar signal modification as a guide for lesion creation during radiofrequency application in the left atrium: prospective study in humans in the setting of paroxysmal atrial fibrillation catheter ablation. Circ Arrhythm Electrophysiol. 2013 Dec;6(6):1095-102. doi: 10.1161/CIRCEP.113.000749. Epub 2013 Oct 4.
Results Reference
background

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Efficacy Rate of Unipolar Polarity Switch for Lesion Assessment in Pulmonary Vein Isolation

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