About this trial
The purpose of this study is to show that Electrocardiogram Ambulatory Monitoring-guided strategy is superior to ElectroPhysiological Study on the rate of alive patients with an appropriate Pacemaker implantation/non-implantation, at 12 months after randomization, in patients with New Onset Persistent Left Bundle Branch Block after Transcatheter Aortic Valve Implantation.
Eligibility criteria
Qualifiers
Presenting with New Onset Persistent Left Bundle Branch Block, defined as a new Left Bundle Branch Block >150 ms that persists at least two days after Transcatheter Aortic Valve Implantation and is stable
With an anticipated life expectancy >1 year
Who consent to participate to the study
Disqualifiers
Documented high grade Atrio Ventricular block (Atrio Ventricular block of a degree higher than Mobitz I)
Persistent PR interval prolongation > 240 ms
Occurrence of syncope or sudden cardiac death,
Identification of any indisputable criteria for Pacemaker implantation
Trial design
Treatments tested in this trial
- Transcatheter Aortic Valve Implantation