Westmead Hospital
Westmead, Australia
Location status: Recruiting
NCT Number: NCT06360939
The goal of this randomized clinical trial is to test the efficacy of stereotactic body radiation therapy (SBRT) in treating ventricular tachycardia (VT) in patients with advanced structural heart disease. The main questions it aims to answer are:
* What is the efficacy of SBRT compared to catheter ablation (CA) in achieving a ≥ 75% reduction in VT burden at 6 months * What is the comparable safety profile of SBRT vs CA Researchers will compare SBRT and CA (standard of care).
Interested in participating?
Request Info18 year and older
All sexes
Interventional
Not applicable
Westmead, Australia
Location status: Recruiting
Hypothesis
We hypothesise that in an open label randomised controlled trial of patients with advanced structural heart disease and ventricular tachycardia (VT) that stereotactic body radiation therapy (SBRT) will be superior in reducing VT burden compared to standard care comprising of catheter ablation (CA) and routine medical care with acceptable safety and adverse events.
Aims
This is a trial to examine if in an open label randomised trial of 60 patients with structural heart disease and VT followed for 3 years with a minimum follow up of 1 year of SBRT compared CA results in:
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Delivery of 25Gy in a single dose fraction to target area within 6 weeks of randomization
CA (endocardial and/or epicardial at operator discretion) within 6 weeks of randomization.
Time frame: 6 months
Change in proportion of patients with a ≥75% reduction in VT burden at 6 months (number of VT episodes in 6 months post treatment compared to the number of VT episodes in the 6 months prior to randomisation excluding a 6-week blanking period after treatment initiation)
Time frame: 6, 12, 24 and 36 months
Recurrent sustained VT ascertained by implanted cardioverter defibrillator (ICD) (VT identified and treated by the ICD with anti-tachycardia pacing (ATP) and/or internal ICD delivered shock or ≥30 seconds of VT if untreated by ICD
Time frame: 6, 12, 24 and 36 months
VT storm (three or more documented episodes of VT within 24 hours or incessant VT)
Time frame: 6, 12, 24 and 36 months
Absolute percentage reduction in VT burden compared to pre-ablation
Time frame: At all time points up to 36 months
Time frame: 6, 12, 24 and 36 months
Implantable Cardioverter Defibrillator shocks
Time frame: 6, 12, 24 and 36 months
Cardiovascular as well as specifically heart failure and arrhythmia
Time frame: 6,12, 24 and 36 months
All cause mortality
Time frame: 6,12, 24 and 36 months
Cardiovascular mortality
Time frame: 6,12, 24 and 36 months
Composite outcome as above
Time frame: 6,12, 24 and 36 months
As determined by echocardiography (ejection fraction, speckle tracking echocardiography)
Time frame: 6,12, 24 and 36 months
Change in quality of life at 6 and 12 months (compared to pre-intervention) as measured by Short Form- 36 (SF-36) [0-100 scale, 0 is equivalent to maximum disability and a score of 100 is equivalent to no disability].
Time frame: 6,12, 24 and 36 months
Change in quality of life at 6 and 12 months (compared to pre-intervention) as measured by Implantable Cardioverter Defibrillator Concerns Questionnaire (ICDC) score. [0-100 scale, 100 equivalent to maximum concern]
Time frame: 6,12, 24 and 36 months
Number of AADs at time points following randomization
Contact information is provided by the study sponsor or research team.
Western Sydney Local Health District
Other
Acronym: RadioAblate-VT
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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