An observational study in Ventricular Tachycardia, Ventricular Fibrillation and Sudden Cardiac Death, sponsored by Universitätsmedizin Mannheim. Status unknown at 1 site in Germany. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2020-08-27.
Sponsored by Universitätsmedizin Mannheim · Observational
The "Registry of Malignant Arrhythmias and Sudden Cardiac Death - Influence of Diagnostics and Interventions (RACE-IT)" represents a mono-centric registry of patients being hospitalized suffering from malignant arrythmias (ventricular tachycardia or fibrillation) and sudden cardiac death (SCD).
Detailed findings of patients' clinical outcome regarding mortality and co-morbidities related to the presence of invasive diagnostics or therapies including coronary angiography, percutaneous coronary intervention (PCI), electrophysiological testing (EP), catheter ablation and implanted cardiac devices (e.g. implantable cardioverter-defibrillators) will be documented. Patients will be included when being hospitalized from the year 2004 until today.
623 studies on the registry are indexed under Tachycardia; 81 are open to participants now.
This study's planned enrollment of 3,200 is above the median of 149 across 208 observational studies indexed under Tachycardia.
Browse Tachycardia studies →Universitätsmedizin Mannheim is the lead sponsor of 75 studies on the registry; 2 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Patients being hospitalized with diagnoses of ventricular tachycardia, ventricular fibrillation and/or sudden cardiac death at the First Department of Medicine, University Medical Centre Mannheim, Germany.
Hospitalization due to:
Exclusion Criteria:
Incidence of ventricular arrythmias (i.e. ventricular fibrillation, ventricular tachykardia, asystole, SCD)
Time frame: Through study completion, potentially up to 12 years, depending on patient inclusion/first event and patients lifetime
Incidence of coronary artery disease (CAD) and PCI in patients with VF/VT/SCD
Time frame: Through study completion, potentially up to 12 years, depending on patient inclusion/first event and patients lifetime
Incidence of invasive electrophysiologic testing (EP) and catheter ablation
Time frame: Through study completion, potentially up to 12 years, depending on patient inclusion/first event and patients lifetime
Incidence of treatment with cardiac devices (i.e. ICD, CCM, CRT-D)
Time frame: Through study completion, potentially up to 12 years, depending on patient inclusion/first event and patients lifetime
Incidences of recurrent malignant tachycardias, all-cause mortality, arrhythmia-related death, re-PCI/ACVB, re-ablation, further therapy with cardiac devices
Time frame: Through study completion, potentially up to 12 years, depending on patient inclusion/first event and patients lifetime
Plan to share: No
This study is status unknown, as verified in Aug 2020. You cannot join it, but the record below documents what was studied.
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Universitätsmedizin Mannheim