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