R Wave Sensing After VT Ablation

Tachycardia, Ventricular Clinical Trial

— RASA-VT  

Official title:

R Wave Sensing After Radiofrequency Ablation of Ventricular Tachycardia Substrate in Patients With Structural Heart Disease

Clinical Trial Details — Status: Not yet recruiting

Administrative data

• NCT number: NCT03779165
• Other study ID #: ZAPSA01
• Secondary ID: UTN U1111-1223-2
• Status: Not yet recruiting
• Start date: December 2018
• Est. completion date: December 2020

Study information

• Verified date: December 2018
• Source: University Hospital "Sestre Milosrdnice"
• Contact: Ivan Zeljkovic, MD
• Phone: 0038513787733
• Email: ivanzeljkov[@]gmail.com
• Is FDA regulated: No
• Study type: Observational [Patient Registry]

Clinical Trial Summary

Sustained, monomorphic ventricular tachycardia (VT) is most commonly encountered in patients with structural heart disease, usually with ischemic aetiology. It has been proven that repeated episodes of sustained VT contribute to the mortality of patients with structural heart disease. These patients are usually implanted with implantable cardioverter defibrillator without (ICD) or with cardiac resynchronisation therapy (CRT-D). According to the current guidelines 3D mapping with radiofrequency (RF) ablation of the tachycardia substrate is an established therapeutic option. As part of the clinical follow-up of patients implanted with cardiac implantable electronic devices (CIED), CIED function parameters are monitored every 6 months, which is always done before and after any procedure involving RF ablation. Furthermore, a transient drop of R wave sensing has been demonstrated after the atrioventricular (AV) node ablation in patients with single-chamber pacemakers and fast atrial fibrillation. The aim of this study is to assess the change in R wave sensing after the RF ablation of VT substrate.

This study will be performed as a clinical, prospective, multi-centre, observational cohort study with a structured follow-up period of 12 months. All consecutive patients with sustained VT implanted with ICD or CRT-D undergoing RF ablation procedure of myocardial substrate, who are able to understand and sign informed consent, will be enrolled. Primary objective is a R wave sensing drop > 30% after VT substrate ablation procedure. Recruiting should not exceed 12 months with the minimal follow-up period of 12 months (24 months in total). Standardized statistical methods and test will be done using SPSS Software Version 22.0 or newer.

This unique study offers the possibility to show the impact of RF ablation on short-term and long-term R wave sensing change assessed by ICD or CRT-D's ventricle electrode in patients with sustained VT and structural heart disease undergoing ablation procedure. This observational data is needed to further refine the treatment of these patients and to prevent possible ICD/CRT-D dysfunction which could endanger this patient population.

Description:

Sustained, monomorphic ventricular tachycardia (VT) is most commonly encountered in patients with structural heart disease, usually with ischemic aetiology. It has been proven that repeated episodes of sustained VT contribute to the mortality of patients with structural heart disease. These patients are usually implanted with implantable cardioverter defibrillator without (ICD) or with cardiac resynchronisation therapy (CRT-D) as part of sudden cardiac death (SCD) prevention and have had activation of the device due to the sustained VT episodes. According to the current guidelines 3D mapping with radiofrequency (RF) ablation of the tachycardia substrate is an established therapeutic option. As part of the clinical follow-up of patients implanted with cardiac implantable electronic devices (CIED), including ICDs and CRT-Ds, function parameters are monitored every 6 months. The same check-up is done before and after any procedure involving RF ablation. Furthermore, a transient drop of R wave sensing has been demonstrated after the RF ablation of the atrioventricular (AV) node in patients with uncontrollable fast atrial fibrillation implanted with single-chamber pacemakers. The above mentioned have not been studied yet in patients ablated due to sustained VT. Hence, the aim of this study is to assess the change in R wave sensing after the RF ablation of VT substrate in patients with structural heart disease.

This study will be performed as a clinical, prospective, multi-centre, observational (analytic, longitudinal) cohort study with patient enrolment in 4 electrophysiology centres in Croatia and Switzerland and a structured follow-up period of 12 months.

All consecutive patients with sustained VT implanted with ICD or CRT-D undergoing RF ablation procedure of myocardial substrate, who are able to understand and sign informed consent, will be enrolled.

Exclusion criteria:

• Patients with combined mechanical aortic and mitral valve prostheses

• Patients with RF ablation of VT done in the last 12 months

• Patients with known damaged ICD/CRT-D electrode or battery

• Patients undergoing VT ablation who have not been implanted with ICD or CRT-D

• Patients not willing or able to undergo clinical follow-up of ICD/CRT-D device

• Patients with life expectancy < 1 year

• Not able to understand or willing to sign informed consent

• Age < 18 years Primary objective is a R wave sensing drop > 30% after VT substrate ablation procedure.

Specific (secondary) end-points:

• incidence of VT recurrence after the ablation procedure;

• risk factors for R wave sensing drop (> 30%) after the RF ablation of VT substrate;

• time needed for R wave sensing recovery after the RF ablation procedure. Recruiting should not exceed 12 months with the minimal follow-up period of 12 months (24 months in total).

The risk categorisation of the study was done and the study was awarded a risk category A.

Sample size was chosen according to annual procedure volumes in Croatia and Switzerland. In addition, it is confirmed by power test (number needed to recruit: 52). Recruiting should not exceed 12 months. Categorical variables will be presented by contingency tables in absolute values and percentages. Categorical variables will be compared by the chi-square with Yates corrections or Fisher`s exact test. Continuous data will be expressed as means and standard deviations or median with corresponding interquartile range. The differences in quantitative variables will be tested by Mann-Whitney U-test (non-parametric test for independent samples). Logistic regression will be used to analyse the association between all variables of interest and the R wave sensing drop. Multivariate logistic regression will be used to adjust for confounding factors. Predictors of the R wave sensing drop will be assessed in a univariate and multivariate Cox proportional hazards model. The statistical analysis will be done using SPSS Software Version 22.0 or newer (IBM SPSS Statistics, New York, USA).

This unique study offers the possibility to show the impact of RF ablation on short-term and long-term R wave sensing change assessed by ICD or CRT-D's ventricle electrode in patients with sustained VT and structural heart disease undergoing ablation procedure. This observational data is needed to further refine the treatment of these patients and to prevent possible ICD/CRT-D dysfunction which could endanger this patient population. Despite a high number of cohort registries for cardiovascular diseases (e.g. Danish heart registry, ORBIT-AF, GARFIELD AF registry, Swiss AF registry), there are scarce data on patients with structural VT and no data regarding R wave sensing changes influenced by RF energy application in ventricles. In addition, this could influence obligatory rhythm-monitoring duration and consequently hospitalization duration of patients with VT undergoing RF ablation procedures. Apart from the above mentioned, in those patients with non-optimal preprocedural R wave sensing, this could mean contraindication for procedure or having the need to do postprocedural defibrillation testing. It is likely, that data from our study will lead to future changes in periprocedural planning and modalities.

This study will be conducted in compliance with the current version of the Declaration of Helsinki, the ICH-GCP or ISO EN 14155 (as far as applicable) as well as all national legal and regulatory requirements. According to ethical regulations, the study plan with the proposed participant information and consent form as well as other project-specific documents will be submitted to Ethic committee of the participating centres.

Recruitment information / eligibility

• Status: Not yet recruiting
• Enrollment: 100
• Est. completion date: December 2020
• Est. primary completion date: December 2019
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• patients with recurrent, sustained ventricular tachycardia

• patients implanted with implantable cardioverter defibrillator (ICD) or cardiac resynchronization therapy cardioverter defibrillator (CRT-D)

• patients planned for 3D mapping and radiofrequency ablation of ventricular tachycardia myocardial substrate

• patients who are able to understand and sign informed consent

Exclusion Criteria:

• Patients with combined mechanical aortic and mitral valve prostheses

• Patients with RF ablation of VT done in the last 12 months

• Patients with known damaged ICD/CRT-D electrode or battery

• Patients undergoing VT ablation who have not been implanted with ICD or CRT-D

• Patients not willing or able to undergo clinical follow-up of ICD/CRT-D device

• Patients with life expectancy < 1 year

• Not able to understand or willing to sign informed consent

• Age < 18 years

Related Conditions & MeSH terms

• Catheter Ablation
• Electrodes
• Follow-Up Studies
• Tachycardia
• Tachycardia, Ventricular

Locations

Country	Name	City	State
Croatia	University Hospital Rijeka	Rijeka
Croatia	University Hospital Sestre milosrdnice	Zagreb
Switzerland	University Hospital Basel	Basel
Switzerland	University Hospital Bern	Bern

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital "Sestre Milosrdnice"

Countries where clinical trial is conducted

Croatia,  Switzerland, 

References & Publications (2)

Darrat YH, Agarwal A, Morales GX, Thompson J, Abdel-Latif A, Waespe K, DI Biase L, Natale A, Patwardan A, Elayi CS. Radiofrequency and Cryo-Ablation Effect on Transvenous Pacing and Defibrillatory Lead Integrity: An In Vitro Study. J Cardiovasc Electrophy — View Citation

Priori SG, Blomström-Lundqvist C, Mazzanti A, Blom N, Borggrefe M, Camm J, Elliott PM, Fitzsimons D, Hatala R, Hindricks G, Kirchhof P, Kjeldsen K, Kuck KH, Hernandez-Madrid A, Nikolaou N, Norekvål TM, Spaulding C, Van Veldhuisen DJ; Task Force for the Ma — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	R wave sensing change	R wave sensing drop > 30% after RF ablation of VT substrate in left and/or right ventricle assessed by ventricular electrode of the CIED	immediately after the ablation procedure
Secondary	R wave sensing change 24h follow-up	R wave sensing drop > 30% after RF ablation of VT substrate in left and/or right ventricle assessed by ventricular electrode of the CIED	24 hours after ablation procedure
Secondary	R wave sensing change 3-6 month follow-up	R wave sensing drop > 30% after RF ablation of VT substrate in left and/or right ventricle assessed by ventricular electrode of the CIED	3-6 months after ablation procedure
Secondary	R wave sensing change 9-12 month follow-up	R wave sensing drop > 30% after RF ablation of VT substrate in left and/or right ventricle assessed by ventricular electrode of the CIED	9-12 months after the ablation procedure
Secondary	Incidence of VT recurrence after the ablation procedure	Assessing the VT recurrence after the ablation procedure by ICD or CRT-D interrogation adn function testing	12 months after the ablation procedure
Secondary	Risk factors for R wave sensing change after the RF ablation of VT substrate	assessing risk factors for R wave sensing drop after the RF ablation of VT substrate	12 months