Ventricular Tachycardia Clinical Trial
Official title:
Phase I/II Study of 4-D Navigated Non-invasive Radiosurgical Ablation of Ventricular Tachycardia
Verified date | December 2022 |
Source | University Hospital Ostrava |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Phase I/II study of 4-D Navigated Non-invasive radiosurgical ablation of ventricular tachycardia (NIRA-VT).
Status | Completed |
Enrollment | 10 |
Est. completion date | January 31, 2020 |
Est. primary completion date | December 31, 2019 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - history of sustained monomorphic VT or termination of monomorphic VT by ICD (appropriate therapy) during previous 6 months prior to enrollment - implantation ICD - inducibility at least one of monomorphic ventricular tachycardia by ICD during EP study with programmed ventricular stimulation - history of myocardial infarction (MI) - left ventricular scar and decreased systolic function of the left ventricle (ejection fraction of left ventricle less than 40%) based on transthoracic ultrasound - stable chronic heart failure (NYHA II-III) - older than 18 years - signed an IRB approved written informed consent document. - failed at least one invasive catheter ablation procedure or have a contraindication to a catheter ablation procedure Exclusion Criteria: - acute myocardial infarction - chronic heart failure NYHA IV - channelopathy - reversible cause of VT (e.g. ionic dysbalance, intoxications) - pregnancy or breastfeeding - history of chest radiotherapy - arrhythmic substrate larger than 100 ccm |
Country | Name | City | State |
---|---|---|---|
Czechia | Hospital Nový Jicín, Nuclear Medicine - PET/CT | Nový Jicín | Moravian-Silesian Region |
Czechia | University Hospital Ostrava | Ostrava | Moravian-Silesian Region |
Czechia | Hospital Podlesí | Trinec | Moravian-Silesian Region |
Lead Sponsor | Collaborator |
---|---|
University Hospital Ostrava | Hospital Nový Jicín, Hospital Podlesi, University of Ostrava |
Czechia,
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* Note: There are 14 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Composite of death | Composite of death occurring at any time after treatment or arrhythmic storm (three or more documented episodes of VT within 24 hours) or appropriate ICD therapy (both shock and pacing) after a 90-day treatment period. 90-day treatment period was imposed to exclude nonfatal outcomes that might occur during acute radiation reaction. Moreover, functional radiosurgery has 90% success rate after 3 months. | 90 days | |
Primary | Acute radiation-induced events | Acute radiation-induced events (within 3 months after treatment) according to CTCAE 4.0. Major concern will be on radiation myocarditis, pericarditis and pneumonitis/fibrosis. Needs of antiemetic drugs will be recorded. | 18 months | |
Primary | Late radiation-induced effects | Late radiation-induced effects (after 3 months after treatment) according to CTCAE 4.0. Major concern will be on radiation myocarditis, pericarditis and pneumonitis/fibrosis. Needs of antiemetic drugs will be recorded. | 18 months | |
Secondary | Time to death at any time | 18 months | ||
Secondary | Time to arrhythmic storm | Time to arrhythmic storm (three or more documented episodes of VT within 24 hours) at any time and after 90-day treatment period. | 90 days | |
Secondary | Time to appropriate ICD shock | Time to appropriate ICD shock at any time and after 90-day treatment period. | 90 days | |
Secondary | Time to appropriate antitachycardial pacing by ICD | Time to appropriate antitachycardial pacing by ICD at any time and after 90-day treatment period. | 90 days | |
Secondary | Hospitalization due to VT | 18 months | ||
Secondary | Hospitalization due to chronic heart failure | 18 months | ||
Secondary | Quality of life measured with EQ-5D questionnaire | Quality of life measurement using a standardised tool named EQ-5D. 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 EQ-5D instrument consists of a descriptive system and the EuroQol-visual analogue scales (EQ VAS). The quality of life is measured in 5 dimensions (mobility, self-care, usual activities, pain/discomfort and anxiety/depression. Each dimension has 3 levels: no problems, some problems, extreme problems. The higher the score achieved, the higher the quality of life of the patient. | 18 months |
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