Ventricular Tachycardia Clinical Trial
Official title:
STereotactic Ablative Radiosurgery of Recurrent Ventricular Tachycardia in Structural Heart Disease
Verified date | October 2020 |
Source | University Hospital Ostrava |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
STereotactic Ablative Radiosurgery of recurrent Ventricular Tachycardia in structural heart disease (STAR-VT).
Status | Withdrawn |
Enrollment | 0 |
Est. completion date | September 30, 2020 |
Est. primary completion date | September 30, 2020 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 30 Years and older |
Eligibility | Inclusion Criteria: - Patients with structural heart disease (ischemic and non-ischemic cardiomyopathy, previous surgery for congenital heart disease) - Implanted ICD or CRT-D (cardiac resynchronization therapy defibrillator) - Prior =1 catheter ablation procedure for monomorphic VT - VT recurrence early (<12 months) after the last ablation with at least 2 episodes of recurrent VT, including 1 episode while on amiodarone (if not contraindicated) - Age =30 years - Signed an IRB-approved (Institutional Review Board) written informed consent Exclusion Criteria: - Acute myocardial infarction or recent percutaneous coronary intervention (PCI) or cardiac surgery (<3 months) - Primary electrical disease (channelopathy) - Reversible cause of VT (e.g. drug-induced, intoxications, etc) - Pregnancy or breastfeeding - Chronic heart failure New York Heart Association (NYHA) Class IV - Serious comorbidities with presumed life expectancy less than one year - Significant peripheral artery disease precluding retrograde aortic mapping - History of chest radiotherapy |
Country | Name | City | State |
---|---|---|---|
Czechia | University Hospital Ostrava | Ostrava-Poruba | Czech Republic |
Czechia | Institute for Clinical and Experimental Medicine Prague | Prague | Central Bohemia |
Czechia | Hospital Podlesí | Trinec | Moravian-Silesian Region |
Lead Sponsor | Collaborator |
---|---|
University Hospital Ostrava | Hospital Podlesí, Institute for Clinical and Experimental Medicine |
Czechia,
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* Note: There are 20 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change of sustained VT burden in three 3-month intervals | Change of sustained VT burden in three 3-month intervals will be assessed. For all arrhythmic events, a 90-day post-radiosurgery blanking period will be applicable. | 50 months | |
Primary | Composite endpoint of (i) all-cause death, (ii) appropriate ICD therapy (both shock and antitachycardia pacing) for VT/VF (ventricular fibrillation) or (iii) sustained VT below the detection threshold | All-cause death, appropriate ICD therapy (both shock and antitachycardia pacing) for VT/VF (ventricular fibrillation) or sustained VT below the detection threshold will be observed for up to 50 months. For all arrhythmic events, a 90-day post-radiosurgery blanking period will be applicable. | 50 months | |
Primary | 3. Rate of acute (<3 months) and late radiation-induced events according to CTCAE 4.0. | The rate of acute (<3 months) and late radiation-induced events according to CTCAE 4.0 will be observed. | 53 months | |
Secondary | Composite endpoint of all-cause death and appropriate ICD shock | The composite endpoint of all-cause death and appropriate ICD shock will be observed for the period of up to 50 months. For all arrhythmic events, a 90-day post-radiosurgery blanking period will be applicable. | 50 months | |
Secondary | Electric storm recurrence | The recurrence of electric storm will be observed. For all arrhythmic events, a 90-day post-radiosurgery blanking period will be applicable. | 53 months | |
Secondary | Cardiovascular hospitalisations | The hospitalisations due to cardiovascular indications will be observed. | 53 months | |
Secondary | Change in quality of life | Change in quality of life will be observed using the standardised EQ-5D (5-dimension) questionnaire. EQ-5D is a standardised instrument in the form of a questionnaire developed by the EuroQol Group as a measure of health-related quality of life that can be used in a wide range of health conditions and treatments. The quality of life is assessed in five dimensions, with three levels in each dimension. The higher score the patient achieves, the better the quality of life. | 53 months |
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