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Post-ablation Alcohol Impacts Arrhythmia Recurrence, Quality of Life and Cognition in AF (PLATINUM)

Primary Purpose

Atrial Fibrillation

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Study arm
Sponsored by
Texas Cardiac Arrhythmia Research Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Atrial Fibrillation focused on measuring Alcohol, AF, catheter ablation, recurrence

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • AF patients that regularly consume >5 alcoholic drink (*12 g of pure alcohol/drink)/week
  • Paroxysmal or persistent AF
  • First catheter ablation History of alcohol-induced arrhythmia
  • Willing to sign the written informed consent

Exclusion Criteria:

  • Binge drinkers (alcohol dependence)
  • Non-drinkers
  • LVEF <35%
  • Psychiatric conditions
  • MoCA score ≤ 17 on Montreal Cognitive Assessment (MoCA)
  • Patients with established dementia
  • Medically unstable patients (acute/unstable or poorly controlled problems that would demand focused, relatively urgent or emergent medical attention)
  • Unwilling for alcohol-abstinence
  • Long-standing persistence AF
  • Patient under legal protection
  • Pregnancy

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Active Comparator

    Active Comparator

    Arm Label

    Study

    Control

    Arm Description

    Complete abstinence or ≤2 drinks/week in group 1 during the study period

    Allowed to continue their pre-ablation drinking habit

    Outcomes

    Primary Outcome Measures

    Arrhythmia recurrence
    Arrhythmia recurrence across all AF types at 8 months after the ablation procedure, off- or on-antiarrhythmic drug (AAD)

    Secondary Outcome Measures

    Change in QoL
    Change in QoL measured by AFEQT survey at baseline and 6 months
    Change in cognitive function
    Change in cognitive function measured by MoCA survey
    Arrhythmia burden
    Arrhythmia burden at follow-up

    Full Information

    First Posted
    August 15, 2022
    Last Updated
    August 18, 2022
    Sponsor
    Texas Cardiac Arrhythmia Research Foundation
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    1. Study Identification

    Unique Protocol Identification Number
    NCT05510167
    Brief Title
    Post-ablation Alcohol Impacts Arrhythmia Recurrence, Quality of Life and Cognition in AF
    Acronym
    PLATINUM
    Official Title
    Impact of Post-ablation Alcohol Intake on Arrhythmia Recurrence, Quality of Life and Cognition in Patients With Atrial Fibrillation
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2022
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    August 22, 2022 (Anticipated)
    Primary Completion Date
    August 2024 (Anticipated)
    Study Completion Date
    August 2025 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Texas Cardiac Arrhythmia Research Foundation

    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
    Earlier studies have shown a dose-dependent relationship between alcohol intake and incident atrial fibrillation (AF) as well as a causal link with several risk factors for AF such as hypertension, obesity and sleep apnea. However, the effect of drinking (alcohol) on post-ablation outcome such as arrhythmia recurrence, quality of life (QoL) and cognitive function in AF patients is unclear. Therefore, we aim to find the answer for a very frequently asked question, "is it safe to continue drinking alcohol (at the pre-ablation level) following catheter ablation OR should the intake be reduced for better outcome?", in this randomized trial.
    Detailed Description
    BACKGROUND Earlier studies have not only reported alcohol-abstinence to be associated with lower recurrence of AF in patients receiving non-ablative antiarrhythmic therapy, but also unfavorable outcome among regular drinkers (high frequency and quantity) compared to non-drinkers undergoing AF ablation (1-3). In a meta-analysis of 14 studies, where the effect measures for AF associated with highest vs lowest alcohol intake were pooled for analysis, not consuming alcohol was observed to be the most favorable in terms of AF risk reduction (4). Larsson et al reported alcohol drinking, even in moderate quantity, to be a risk factor for incident AF, whereas Zhang et al observed moderate drinking to be associated with high AF risk in men only and not in females (5, 6). Moreover, a causal link between alcohol intake and other cardiovascular morbidities such as obesity, hypertension, left ventricular dysfunction and sleep apnea that are known risk factors for AF has been documented by several studies (1). Thus, we know that alcohol consumption, even in moderate quantity, increases the risk for AF, although may not be across genders. Observational studies also have shown unfavorable procedure outcome to be more common in drinkers compared to non-drinkers receiving AF ablation. However, there is no randomized data to support the latter statement. Additionally, there are no data on the influence of alcohol intake on the cognitive function and QoL in AF patients receiving catheter ablation. Therefore, this investigator-initiated, randomized trial has been designed to examine the impact of alcohol intake vs abstinence on arrhythmia recurrence and burden, QoL and cognitive function in regular drinkers undergoing their first catheter ablation. STUDY RATIONALE We hypothesize that alcohol-abstinence will significantly improve the procedural outcome, QoL and cognitive function in the study population compared to the non-abstinence cohort. STUDY OBJECTIVES Primary Objective Arrhythmia recurrence across all AF types at 8 months after the ablation procedure, off- or on-antiarrhythmic drug (AAD) Secondary Objective 1) Change in QoL score measured by AFEQT survey at baseline and 6 months 2) Change in cognitive function measured by MoCA survey 3) Arrhythmia burden at follow-up Study period will start from the day after the procedure and continue for 8 months (2-month blanking period+ 6 months follow-up). Group 1: Complete abstinence or ≤2 drinks/week in group 1 during the study period Group 2: Allowed to continue their pre-ablation drinking habit

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Atrial Fibrillation
    Keywords
    Alcohol, AF, catheter ablation, recurrence

    7. Study Design

    Primary Purpose
    Other
    Study Phase
    Not Applicable
    Interventional Study Model
    Parallel Assignment
    Model Description
    Paroxysmal and Persistent AF patients undergoing their first catheter ablation will be screened for eligibility and those that meet the criteria and consent to participate will be randomly assigned to group 1 or 2. Study period will start from the day after the procedure and continue for 8 months (2-month blanking period+ 6 months follow-up). Group 1: Complete abstinence or ≤2 drinks/week in group 1 during the study period Group 2: Allowed to continue their pre-ablation drinking habit
    Masking
    None (Open Label)
    Allocation
    Randomized
    Enrollment
    130 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Study
    Arm Type
    Active Comparator
    Arm Description
    Complete abstinence or ≤2 drinks/week in group 1 during the study period
    Arm Title
    Control
    Arm Type
    Active Comparator
    Arm Description
    Allowed to continue their pre-ablation drinking habit
    Intervention Type
    Behavioral
    Intervention Name(s)
    Study arm
    Intervention Description
    Participants will be asked to completely abstain from drinking or consume 2 or less drinks per week for 8 months following catheter ablation
    Primary Outcome Measure Information:
    Title
    Arrhythmia recurrence
    Description
    Arrhythmia recurrence across all AF types at 8 months after the ablation procedure, off- or on-antiarrhythmic drug (AAD)
    Time Frame
    8 months after the ablation procedure for AF
    Secondary Outcome Measure Information:
    Title
    Change in QoL
    Description
    Change in QoL measured by AFEQT survey at baseline and 6 months
    Time Frame
    6 months after the blanking period of 2 months
    Title
    Change in cognitive function
    Description
    Change in cognitive function measured by MoCA survey
    Time Frame
    6 months after the blanking period of 2 months
    Title
    Arrhythmia burden
    Description
    Arrhythmia burden at follow-up
    Time Frame
    6-8 months following ablation

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    18 Years
    Maximum Age & Unit of Time
    85 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: AF patients that regularly consume >5 alcoholic drink (*12 g of pure alcohol/drink)/week Paroxysmal or persistent AF First catheter ablation History of alcohol-induced arrhythmia Willing to sign the written informed consent Exclusion Criteria: Binge drinkers (alcohol dependence) Non-drinkers LVEF <35% Psychiatric conditions MoCA score ≤ 17 on Montreal Cognitive Assessment (MoCA) Patients with established dementia Medically unstable patients (acute/unstable or poorly controlled problems that would demand focused, relatively urgent or emergent medical attention) Unwilling for alcohol-abstinence Long-standing persistence AF Patient under legal protection Pregnancy
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Andrea Natale
    Phone
    5125448186
    Email
    dr.natale@gmail.com
    First Name & Middle Initial & Last Name or Official Title & Degree
    Sanghamitra Mohanty
    Phone
    5127842651
    Email
    mitra1989@gmail.com
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Andrea Natale
    Organizational Affiliation
    Texas Cardiac Arrhythmia Institute, St.
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

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