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Efficacy and Safety of Epicardial VT Ablation Using Contact Force Irrigated Tip Catheter - Pilot Study

Primary Purpose

Tachycardia, Ventricular

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Epicardial VT ablation
Endocardial VT Ablation
Sponsored by
University of Sao Paulo General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Tachycardia, Ventricular focused on measuring Ventricular Tachycardia, RF ablation, Epicardial Access, Contact Sensor Irrigated tip catheter

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with ischemic and non-ischemic cardiomyopathy and recurrent sustained monomorphic VT requiring cardioversion or antiarrhythmic drug administration with ≥4 episodes in the previous 6 months despite an ICD or antiarrhythmic drug therapy.
  • Patients without ICD were eligible after 2 episodes of sustained VT.

Exclusion Criteria:

  • Creatinine level >2.5mg/dL
  • LV ejection fraction <10%
  • NYHA Class IV
  • Mobile thrombus on LV
  • Absence of vascular access to the LV
  • Life-expectancy of less than 12 months
  • Previous open-chest cardiac surgical procedure
  • Unstable angina; myocardial infarction in the last 2 months
  • Severe aortic stenosis
  • Severe mitral regurgitation secondary to leaflet or chordae rupture
  • Pregnancy and age of less than 18 years old.

Sites / Locations

  • Arrhythmia Clinical Unit - Instituto do Coração - HCFMUSP

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Epicardial VT ablation

Endocardial VT Ablation

Arm Description

Patients will underwent combined epicardial and endocardial mapping and ablation

Patients will underwent endocardial only VT mapping and ablation

Outcomes

Primary Outcome Measures

Efficacy of epicardial ablation
We will evaluate if the procedure was succeeded according to reinducibility of ventricular tachycardia. We consider success as follows: (1) Complete Success: prevention of induction of any VT following ablation; (2) Partial Success: prevention of induction of the clinical VT, remaining the induction of at least one non-clinical faster VT; (3) Failure: Remaining the induction of the clinical or initially induced VT.

Secondary Outcome Measures

Safety of epicardial access
We will evaluate the rate of complications related to the epicardial access.
Safety of epicardial ablation using irrigated contact sensor catheter
We will evaluate the rate of complications related to irrigated tip catheter use on epicardial surface.

Full Information

First Posted
February 20, 2014
Last Updated
April 19, 2020
Sponsor
University of Sao Paulo General Hospital
Collaborators
Biosense Webster, Inc.
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1. Study Identification

Unique Protocol Identification Number
NCT02072707
Brief Title
Efficacy and Safety of Epicardial VT Ablation Using Contact Force Irrigated Tip Catheter - Pilot Study
Official Title
Prospective and Randomized Study to Evaluate Efficacy and Safety of Epicardial Ventricular Tachycardia Ablation Using Contact Force Sensor Irrigated Tip Catheter - Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Completed
Study Start Date
April 2014 (undefined)
Primary Completion Date
July 21, 2017 (Actual)
Study Completion Date
July 21, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Sao Paulo General Hospital
Collaborators
Biosense Webster, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators hypothesized that combined endocardial and epicardial VT ablation using contact sensor irrigated catheter is safe and achieves a lower recurrence rate than endocardial only ablation in ischemic and non-ischemic patients, for this the investigators will randomize 20 patients in two groups, one with endocardial only ablation and other with combined endocardial and epicardial ablation.
Detailed Description
Pilot Study Design The investigators will select 20 ischemic or non-ischemic cardiomyopathy patients with scar related Ventricular tachycardia with indication of VT ablation. After informed consent, these patients will be randomized to endocardial only (Control Group) or combined endocardial and epicardial ablation (Treatment Group). Inclusion Criteria Patients with ischemic and non-ischemic cardiomyopathy and recurrent sustained monomorphic VT requiring cardioversion or antiarrhythmic drug administration with ≥4 episodes in the previous 6 months despite an ICD or antiarrhythmic drug therapy. Patients without ICD were eligible after 2 episodes of sustained VT. Exclusion Criteria Creatinine level >2.5mg/dL; LV ejection fraction <10%; NYHA Class IV; mobile thrombus on LV; absence of vascular access to the LV; life-expectancy of less than 12 months; previous open-chest cardiac surgical procedure; unstable angina; myocardial infarction in the last 2 months; severe aortic stenosis; severe mitral regurgitation secondary to leaflet or chordae rupture; pregnancy and age of less than 18 years old. Ablation Technique In the patients randomized for combined epicardial and endocardial ablation, subxyphoid puncture will be performed according to previously described technique. Following successful epicardial access on the combined epi and endocardial ablation and following the venous puncture on the endocardial only group, a puncture of femoral artery will be performed. If the patient has peripheral artery disease, the catheter will be positioned on the left ventricle through transeptal puncture. Electroanatomic voltage map will be constructed of the endocardial and epicardial surface. After map construction, programmed ventricular stimulation of the apex of the RV with S4 extrastimuli will be performed aiming for VT inducibility. If the induced VT is well tolerated, activation mapping of the VT will be constructed in addition to entrainment mapping. If the VT is not hemodynamically tolerated, it will be reverted either by Burst or electrical cardioversion, than substrate modification in the scar combined with pace-mapping and local abnormal electrograms (late potentials) ablation will be performed. In the patients in the endocardial only group, only the endocardial surface of the right or left ventricle will be ablated. In the combined epicardial and endocardial group, the choice of the surface to be ablated will be guided by the tachycardia mapping (mesodiastolic and pre-systolic potentials), extension of the scar, pace-mapping in both surfaces. ECG criteria suggesting epicardial surface will also be considered to define the epi or endo surface to be ablated. Following ablation, a repeated programmed ventricular stimulation with S4 will be performed to evaluated reinducibility of the VT. Additional RF applications can be performed according to clinical criteria, and the procedure will be considered terminate when no VT is inducible or by clinical criteria. In the endo only group that endocardial scar could not be observed or following extensive endocardial ablation the clinical VT still remain inducible, and the ECG criteria suggests epicardial VT will underwent epicardial mapping and ablation and this will be considered as a Cross-over. Outcomes Primary Outcome: Safety: The investigators will evaluate the rate of complications related to irrigated tip catheter use on epicardial surface. It is expected that the combined epicardial and endocardial ablation group do not present an increase in the rate of catheter-related complications. Efficacy: The investigators will evaluate if the procedure was succeeded. The investigators consider success as follows: (1) Complete Success: prevention of induction of any VT following ablation; (2) Partial Success: prevention of induction of the clinical VT, remaining the induction of at least one non-clinical faster VT; (3) Failure: Remaining the induction of the clinical or initially induced VT. Secondary Outcome: Safety: The investigators will evaluate the rate of complications related to the epicardial access. It is expected a rate of hemopericardium of no more than 20%, with less than 5% rate of major complications as procedure related death, cardiac surgery due to cardiac perforation or blood cell transfusion.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tachycardia, Ventricular
Keywords
Ventricular Tachycardia, RF ablation, Epicardial Access, Contact Sensor Irrigated tip catheter

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Epicardial VT ablation
Arm Type
Active Comparator
Arm Description
Patients will underwent combined epicardial and endocardial mapping and ablation
Arm Title
Endocardial VT Ablation
Arm Type
Active Comparator
Arm Description
Patients will underwent endocardial only VT mapping and ablation
Intervention Type
Procedure
Intervention Name(s)
Epicardial VT ablation
Intervention Description
Combined Epicardial and Endocardial VT Ablation
Intervention Type
Procedure
Intervention Name(s)
Endocardial VT Ablation
Intervention Description
Endocardial Only VT ablation
Primary Outcome Measure Information:
Title
Efficacy of epicardial ablation
Description
We will evaluate if the procedure was succeeded according to reinducibility of ventricular tachycardia. We consider success as follows: (1) Complete Success: prevention of induction of any VT following ablation; (2) Partial Success: prevention of induction of the clinical VT, remaining the induction of at least one non-clinical faster VT; (3) Failure: Remaining the induction of the clinical or initially induced VT.
Time Frame
Programed ventricular stimulation performed 5 minutes after complete ablation
Secondary Outcome Measure Information:
Title
Safety of epicardial access
Description
We will evaluate the rate of complications related to the epicardial access.
Time Frame
24 hours after the procedure
Title
Safety of epicardial ablation using irrigated contact sensor catheter
Description
We will evaluate the rate of complications related to irrigated tip catheter use on epicardial surface.
Time Frame
At the end of the procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with ischemic and non-ischemic cardiomyopathy and recurrent sustained monomorphic VT requiring cardioversion or antiarrhythmic drug administration with ≥4 episodes in the previous 6 months despite an ICD or antiarrhythmic drug therapy. Patients without ICD were eligible after 2 episodes of sustained VT. Exclusion Criteria: Creatinine level >2.5mg/dL LV ejection fraction <10% NYHA Class IV Mobile thrombus on LV Absence of vascular access to the LV Life-expectancy of less than 12 months Previous open-chest cardiac surgical procedure Unstable angina; myocardial infarction in the last 2 months Severe aortic stenosis Severe mitral regurgitation secondary to leaflet or chordae rupture Pregnancy and age of less than 18 years old.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Maurício Scanavacca, MD, PhD
Organizational Affiliation
Instituto do coração - HC/FMUSP
Official's Role
Principal Investigator
Facility Information:
Facility Name
Arrhythmia Clinical Unit - Instituto do Coração - HCFMUSP
City
Sao Paulo
State/Province
SP
ZIP/Postal Code
05403-000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
32087356
Citation
Pisani CF, Romero J, Lara S, Hardy C, Chokr M, Sacilotto L, Wu TC, Darrieux F, Hachul D, Kalil-Filho R, Di Biase L, Scanavacca M. Efficacy and safety of combined endocardial/epicardial catheter ablation for ventricular tachycardia in Chagas disease: A randomized controlled study. Heart Rhythm. 2020 Sep;17(9):1510-1518. doi: 10.1016/j.hrthm.2020.02.009. Epub 2020 Feb 20.
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Efficacy and Safety of Epicardial VT Ablation Using Contact Force Irrigated Tip Catheter - Pilot Study

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