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Subcutaneous ICD Therapy Combined With VT Ablation for the Secondary Prevention of Sudden Cardiac Death

Primary Purpose

Sudden Cardiac Death

Status
Unknown status
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Subcutaneous ICD Therapy Combined with VT Ablation
Sponsored by
Sheba Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Sudden Cardiac Death focused on measuring Subcutaneous ICD Therapy, VT Ablation

Eligibility Criteria

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

Inclusion Criteria:

  • Any scar related sustained VT or VF
  • Class I, IIa, or IIb indication for secondary prevention ICD therapy per ESC Guidelines
  • Age ≥ 22 years on a date of consent
  • LVEF ≤ 40%
  • Positive ECG screening for S-ICD

Exclusion Criteria:

  • A requirement for antibradycardia pacing or CRTD
  • Subjects with an existing ICD, CRT, CRT-D, or pacemaker device.
  • Contraindications for S-ICD implantation
  • Contraindications for VT ablation
  • Serious known concomitant disease with a life expectancy of < 1 year
  • Elderly patients >80 years of age
  • NYHA class IV or need for mechanical LV support (ECMO)
  • Pregnancy or nursing
  • Unwilling or unable to give informed consent

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    S-ICD therapy combined with VT Ablation

    Arm Description

    To evaluate the feasibility and safety of a management approach that incorporates VT-ablation and S-ICD implantation in secondary prevention patients

    Outcomes

    Primary Outcome Measures

    arrhythmic event
    Occurrence of treated arrhythmic event (appropriate and inappropriate). The primary endpoint will be assessed by patient interview, clinical examination, and regularly scheduled SICD interrogation during follow-up

    Secondary Outcome Measures

    Appropriate ICD therapy
    Rate of appropriate ICD therapy (defined as a shock therapy for ventricular tachycardia or fibrillation). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.
    Inappropriate ICD therapy
    Rate of inappropriate therapy (defined as any ICD shock delivered for Non-VT event). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.
    Ablation success rates
    Rate of ablation success (defined as absence of Ventricular Arrhythmia). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.

    Full Information

    First Posted
    June 5, 2018
    Last Updated
    August 22, 2018
    Sponsor
    Sheba Medical Center
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    1. Study Identification

    Unique Protocol Identification Number
    NCT03622307
    Brief Title
    Subcutaneous ICD Therapy Combined With VT Ablation for the Secondary Prevention of Sudden Cardiac Death
    Official Title
    Subcutaneous ICD Therapy Combined With VT Ablation for the Secondary Prevention of Sudden Cardiac Death
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    August 2018
    Overall Recruitment Status
    Unknown status
    Study Start Date
    October 2018 (Anticipated)
    Primary Completion Date
    October 1, 2019 (Anticipated)
    Study Completion Date
    October 1, 2019 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    Sheba Medical Center

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    Yes
    Product Manufactured in and Exported from the U.S.
    Yes

    5. Study Description

    Brief Summary
    This study evaluates the feasibility and safety of a management approach that incorporates VT-ablation and S-ICD implantation in secondary prevention patients. This is a single arm prospective study with 30 patients eligible for implantation of an ICD for the secondary prevention of sudden cardiac death.
    Detailed Description
    The subcutaneous ICD (S-ICD) is a system without transvenous leads that has been proven to safely provide defibrillation for patients at risk of sudden cardiac death due to ventricular tachyarrhythmias. However this system is currently not able to perform anti tachycardia pacing (ATP) which can terminate some VT, thus avoiding painful shocks. Ideally slow VT should be managed with RF ablation while fast VT causing hemodynamic consequences should be treated with ICD shocks combined with medications. Typically, ICDs in secondary prevention patients are programmed to intervene at 10 msec at least above the clinical VT. In cases of hemodynamically stable VT this can result in unnecessary therapies and lead to ICD shocks. S-ICD can safely manage fast VTs while slower hemodynamically VTs can be managed with ablation. This approach can avoid transvenous ICD related complications and unnecessary ICD interventions such as ATP which can accelerate VT to ICD shock zone. However, the benefit of this management strategy compared to conventional transvenous ICD programming has not been studied in patients who receive the device for the secondary prevention of sudden cardiac death.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Sudden Cardiac Death
    Keywords
    Subcutaneous ICD Therapy, VT Ablation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    30 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    S-ICD therapy combined with VT Ablation
    Arm Type
    Experimental
    Arm Description
    To evaluate the feasibility and safety of a management approach that incorporates VT-ablation and S-ICD implantation in secondary prevention patients
    Intervention Type
    Device
    Intervention Name(s)
    Subcutaneous ICD Therapy Combined with VT Ablation
    Intervention Description
    S-ICD implantation and VT ablation/substrate modification among patients with a secondary prevention indication for an ICD
    Primary Outcome Measure Information:
    Title
    arrhythmic event
    Description
    Occurrence of treated arrhythmic event (appropriate and inappropriate). The primary endpoint will be assessed by patient interview, clinical examination, and regularly scheduled SICD interrogation during follow-up
    Time Frame
    24 months
    Secondary Outcome Measure Information:
    Title
    Appropriate ICD therapy
    Description
    Rate of appropriate ICD therapy (defined as a shock therapy for ventricular tachycardia or fibrillation). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.
    Time Frame
    24 months
    Title
    Inappropriate ICD therapy
    Description
    Rate of inappropriate therapy (defined as any ICD shock delivered for Non-VT event). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.
    Time Frame
    24 months
    Title
    Ablation success rates
    Description
    Rate of ablation success (defined as absence of Ventricular Arrhythmia). This will be assessed by patient interview and regularly scheduled ICD interrogation during follow-up.
    Time Frame
    24 months
    Other Pre-specified Outcome Measures:
    Title
    All cause mortality
    Description
    Rate of all cause mortality. This will be assessed during patient follow up.
    Time Frame
    24 months
    Title
    Cardiac mortality
    Description
    Rate of all cardiac mortality. This will be assessed during patient follow up.
    Time Frame
    24 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    22 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Any scar related sustained VT or VF Class I, IIa, or IIb indication for secondary prevention ICD therapy per ESC Guidelines Age ≥ 22 years on a date of consent LVEF ≤ 40% Positive ECG screening for S-ICD Exclusion Criteria: A requirement for antibradycardia pacing or CRTD Subjects with an existing ICD, CRT, CRT-D, or pacemaker device. Contraindications for S-ICD implantation Contraindications for VT ablation Serious known concomitant disease with a life expectancy of < 1 year Elderly patients >80 years of age NYHA class IV or need for mechanical LV support (ECMO) Pregnancy or nursing Unwilling or unable to give informed consent

    12. IPD Sharing Statement

    Learn more about this trial

    Subcutaneous ICD Therapy Combined With VT Ablation for the Secondary Prevention of Sudden Cardiac Death

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