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Left Bundle Branch Block after Transcatheter Aortic Valve Implantation (TAVI)

Left Bundle Branch Block after Transcatheter Aortic Valve Implantation (TAVI) - LBBB-TAVI

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON34321
Enrollment
40
Registered
2010-09-02
Start date
2010-09-06
Completion date
Unknown
Last updated
2024-06-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

conduction disorder of het heart left bundle branch block

Interventions

None listed

Sponsors

Catharina-ziekenhuis
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: patients planned/accepted for transcatheter aortic valve implantation

Exclusion criteria

Exclusion criteria: inability to give informed consent

Design outcomes

Primary

MeasureTime frame
1. To compare the extent of reversal of left ventricular remodelling at 3 months and 1 year after a TAVI procedure between patients with a TAVI-induced LBBB and TAVI patients without LBBB. Left ventricular remodelling will be defined using echocardiographic parameters (left ventricular endsystolic diameter, left ventricular ejection fraction, left ventricular mass, global longitudinal and circumferential 2D-strain). 2. To evaluate and compare the immediate and long-term effects of a TAVI-induced and non-TAVI-induced LBBB on the ECG, regional and global 2D-strain profile of the left ventricle in a circumferential and longitudinal direction. 2D-Strain will be measured by post-processing of B-mode echocardiographic images (speckle tracking).

Secondary

MeasureTime frame
1. To compare the TAVI-induced LBBB ECG profile and 2D-strain pattern to that of patients with spontaneous LBBB in order to discriminate a proximal from distal LBBB. 2. To correlate the ECG profile and 2D-strain of TAVI-induced LBBB with that of CRT patients with LBBB and indicate whether a dyssynchrony caused by TAVI-induced LBBB is likely to respond to CRT. 3. To evaluate the feasibility of 3D-TOE in guiding placement of the aortic tissue valve during TAVI procedure

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)