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Pulmonary Vein Isolation Strategy of Very High Power Short Duration in Patients With Paroxysmal Atrial Fibrillation

Primary Purpose

Paroxysmal Atrial Fibrillation

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
QDOT MicroTM catheter
AI-guided ablation only for PVI
Sponsored by
Seoul National University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Paroxysmal Atrial Fibrillation

Eligibility Criteria

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

Inclusion Criteria: Patients undergoing PVI for PAF Exclusion Criteria: Aged less than 19 years Patients with persistent AF Patients with previous ablation or surgery for AF Patients with intracardiac thrombus or thromboembolic events within the previous 90 days Patients with cardiac surgery or acute coronary syndrome within the previous 90 days Patients with contraindication(s) for using oral anticoagulants Patients with LA anteroposterior diameter of more than 55 mm Patients with left ventricular ejection fraction less than 35% Pregnants or those who plan to become pregnant during the study Life expectancy less than a year

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm 3

    Arm Type

    Experimental

    Experimental

    Experimental

    Arm Label

    vHPSD ablation only for PVI

    vHPSD and AI-guided ablation for PVI

    AI-guided ablation only for PVI

    Arm Description

    Pulmonary vein encirclement is achieved using contiguous applications of very high power and short duration (90 W over 4 seconds). The inter-lesion distance is set at 3-4mm for the roofs and anterior segments, and 5-6mm for other segments. If the esophageal temperature rises > 38 for segments near the esophagus, encirclement will be applied at 25 W for 15 seconds.

    At the anterior segments, pulmonary vein encirclement is achieved through contiguous applications using AI-guided ablation (40-50 W, AI target 500, and an inter-lesion distance of 4mm). In the other segments, pulmonary vein encirclement is achieved through contiguous applications using very high-power and short-duration techniques (90 W over 4 seconds, inter-lesion distance of 3-4mm; if the segments are near the esophagus, encirclement will be applied at 25 W for 15 seconds).

    Pulmonary vein encirclement is achieved through contiguous applications using AI-guided ablation (40-50 W, AI target 500 for anterior segments and 400 for other segments, with an inter-lesion distance of 4mm; if the segments are near the esophagus, encirclement will be applied at 25 W for 15 seconds)

    Outcomes

    Primary Outcome Measures

    Time for AF ablation
    Including total PVI time, total ablation time, fluoroscopic time, and total procedure time.

    Secondary Outcome Measures

    Acute PV reconnection rate
    Including residual PV potential and early reconnection after 1st pass PVI.
    The segment of residual PV potential
    Descript as RSPV roof/anterior/posterior, RIPV anterior/posterior/inferior, Rt carina, LSPV roof/anterior(ridge)/posterior, LIPV anterior(ridge)/posterior/inferior, Lt carina.
    The segment of early reconnection
    Descript as RSPV roof/anterior/posterior, RIPV anterior/posterior/inferior, Rt carina, LSPV roof/anterior(ridge)/posterior, LIPV anterior(ridge)/posterior/inferior, Lt carina.
    1-year AF recurrence
    Using single lead 3-day holter monitoring.
    30-day complication associated with procedure
    Including puncture site hematoma, puncture site pseudoaneurysm, puncture site AV fistula, stroke, TIA, thromboembolism, and others.

    Full Information

    First Posted
    August 1, 2023
    Last Updated
    August 22, 2023
    Sponsor
    Seoul National University Hospital
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05996159
    Brief Title
    Pulmonary Vein Isolation Strategy of Very High Power Short Duration in Patients With Paroxysmal Atrial Fibrillation
    Official Title
    Pulmonary Vein Isolation Strategy of Very High Power Short Duration in Patients With Paroxysmal Atrial Fibrillation: Q-INDEX Trial
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    July 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    October 1, 2023 (Anticipated)
    Primary Completion Date
    September 30, 2025 (Anticipated)
    Study Completion Date
    September 30, 2026 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Seoul National University Hospital

    4. Oversight

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

    5. Study Description

    Brief Summary
    This study aims to investigate the effect of reducing ablation time for a hybrid approach of vHPSD and AI-guided ablation using the QDOT Micro catheter in PVI among patients with PAF.
    Detailed Description
    Radiofrequency catheter ablation has become a cornerstone strategy for the rhythm control of AF. During the last decade, catheter technology has revolutionized and, accordingly, clinical outcomes after the ablation and procedural efficacy have been improved. In recent years, the use of the CLOSE protocol employing contiguous, closely spaced applications and targeted ablation index (AI) values has translated into robust acute and long-term success rates for PVI, typically with the power delivery of up to 35 W, and more recently with 40 to 50 W, in power and temperature-controlled mode. Contiguous ablation using very high-power, short-duration ablation at 90 W over 4 seconds is expected to shorten procedure time. However, changes in lesion geometry and the altered impact of catheter stability on lesion quality may influence procedural efficiency, safety, and effectiveness. The Q-FFICIENCY trial showed that the vHPSD (90 W, 4 sec), temperature-controlled radiofrequency ablation (25/50 W) has comparable efficacy to conventional-power temperature-controlled ablation. However, the efficacy of vHPSD ablation may depend on PV thickness due to its lesion characteristics. Therefore, AI-guided ablation may have merits over vHPSD ablation in thickened PV segments. According to the POWER PLUS trial, the proportion of 1st-pass PVI with vHPSD ablation was numerically lower than that of the conventional ablation, although there was marginal significance; 83.9% vs. 90.0%, p-value =0.085. According to the OPTIMUM trial, a study conducted by our group, roof and anterior walls of the left atrium often require higher AI targets due to their thickness. Therefore, a hybrid approach that combines both vHPSD and AI-guided ablations according to PV segments may achieve both high efficacy and short ablation time for PVI. The investigators of the POWER PLUS trial also speculated that the hybrid approach based on tissue thickness might offer the optimal balance of procedural efficacy. However, up to date, no studies have investigated the efficacy and safety of the hybrid approach for PVI. More data is needed to suggest that the hybrid approach could be useful for PVI. Therefore, this study aims to investigate the effect of reducing ablation time for a hybrid approach of vHPSD and AI-guided ablation using the QDOT Micro catheter in PVI among patients with PAF.

    6. Conditions and Keywords

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

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    150 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    vHPSD ablation only for PVI
    Arm Type
    Experimental
    Arm Description
    Pulmonary vein encirclement is achieved using contiguous applications of very high power and short duration (90 W over 4 seconds). The inter-lesion distance is set at 3-4mm for the roofs and anterior segments, and 5-6mm for other segments. If the esophageal temperature rises > 38 for segments near the esophagus, encirclement will be applied at 25 W for 15 seconds.
    Arm Title
    vHPSD and AI-guided ablation for PVI
    Arm Type
    Experimental
    Arm Description
    At the anterior segments, pulmonary vein encirclement is achieved through contiguous applications using AI-guided ablation (40-50 W, AI target 500, and an inter-lesion distance of 4mm). In the other segments, pulmonary vein encirclement is achieved through contiguous applications using very high-power and short-duration techniques (90 W over 4 seconds, inter-lesion distance of 3-4mm; if the segments are near the esophagus, encirclement will be applied at 25 W for 15 seconds).
    Arm Title
    AI-guided ablation only for PVI
    Arm Type
    Experimental
    Arm Description
    Pulmonary vein encirclement is achieved through contiguous applications using AI-guided ablation (40-50 W, AI target 500 for anterior segments and 400 for other segments, with an inter-lesion distance of 4mm; if the segments are near the esophagus, encirclement will be applied at 25 W for 15 seconds)
    Intervention Type
    Device
    Intervention Name(s)
    QDOT MicroTM catheter
    Intervention Description
    Novel high power-short duration ablation catheter for atrial fibrillation
    Intervention Type
    Device
    Intervention Name(s)
    AI-guided ablation only for PVI
    Intervention Description
    Ablation is the removal or destruction of something from an object by vaporization, chipping, erosive processes, or by other means.
    Primary Outcome Measure Information:
    Title
    Time for AF ablation
    Description
    Including total PVI time, total ablation time, fluoroscopic time, and total procedure time.
    Time Frame
    up to 12 months
    Secondary Outcome Measure Information:
    Title
    Acute PV reconnection rate
    Description
    Including residual PV potential and early reconnection after 1st pass PVI.
    Time Frame
    up to 12 months
    Title
    The segment of residual PV potential
    Description
    Descript as RSPV roof/anterior/posterior, RIPV anterior/posterior/inferior, Rt carina, LSPV roof/anterior(ridge)/posterior, LIPV anterior(ridge)/posterior/inferior, Lt carina.
    Time Frame
    up to 12 months
    Title
    The segment of early reconnection
    Description
    Descript as RSPV roof/anterior/posterior, RIPV anterior/posterior/inferior, Rt carina, LSPV roof/anterior(ridge)/posterior, LIPV anterior(ridge)/posterior/inferior, Lt carina.
    Time Frame
    up to 12 months
    Title
    1-year AF recurrence
    Description
    Using single lead 3-day holter monitoring.
    Time Frame
    up to 12 months
    Title
    30-day complication associated with procedure
    Description
    Including puncture site hematoma, puncture site pseudoaneurysm, puncture site AV fistula, stroke, TIA, thromboembolism, and others.
    Time Frame
    up to 12 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    19 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Patients undergoing PVI for PAF Exclusion Criteria: Aged less than 19 years Patients with persistent AF Patients with previous ablation or surgery for AF Patients with intracardiac thrombus or thromboembolic events within the previous 90 days Patients with cardiac surgery or acute coronary syndrome within the previous 90 days Patients with contraindication(s) for using oral anticoagulants Patients with LA anteroposterior diameter of more than 55 mm Patients with left ventricular ejection fraction less than 35% Pregnants or those who plan to become pregnant during the study Life expectancy less than a year

    12. IPD Sharing Statement

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    Pulmonary Vein Isolation Strategy of Very High Power Short Duration in Patients With Paroxysmal Atrial Fibrillation

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