Improving Patient Reported Outcome Measures in Catheter Ablation
Ventricular Tachycardia, ICD, Quality of Life
About this trial
This is an interventional health services research trial for Ventricular Tachycardia focused on measuring Catheter ablation, Patient reported outcome measure, Incremental cost effectiveness ratio
Eligibility Criteria
Inclusion Criteria:
Adults (>18 years) With an Implantable Cardioverter Defibrillator (ICD) implanted >3 months from time of recruitment and a previous episode of documented VT requiring therapy from the ICD.
And impaired LV/RV function Willing and able to give written informed consent
Exclusion Criteria:
Patients who are planning to move away from study site within 12 months of enrolment who wished to use postal method to complete their HRQL Patients who are unable to give informed consent
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Intervention
Comparator
Patients undergoing catheter ablation of VT
Patients undergoing AAD therapy for VT