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A study of an abnormal heart rhythm occurring after transcatheter aortic valve implantation and its effect on survival - a United Kingdom experience.

New left bundle branch block following transcatheter aortic valve implantation and its effect on survival - a United Kingdom experience.

Status
Unknown
Phases
Unknown
Study type
Observational
Source
ISRCTN
Registry ID
ISRCTN11188205
Enrollment
400
Registered
2015-04-30
Start date
2015-02-18
Completion date
Unknown
Last updated
2021-07-26

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

Conditions

Transcatheter aortic valve implantation for the percutaneous treatment of calcific degenerative aortic valve stenosis. Circulatory System

Interventions

Left bundle branch block (LBBB) is the most common conduction abnormality following transcatheter aortic valve implantation (TAVI). Whilst LBBB in the post surgical and heart failure population is kno

Sponsors

King's College London
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: All patients undergoing successful transcatheter aortic valve implantation (TAVI), irrespective of device manufacturer, from the inception of the TAVI programme at the participating institution until the 31st December 2013

Exclusion criteria

Exclusion criteria: 1. Previous/pre-existing permanent pacemaker in situ 2. Unsuccessful transcatheter aortic valve implantation procedure

Design outcomes

Primary

MeasureTime frame
All-cause mortality at 1 year following transcatheter aortic valve implantation.

Secondary

MeasureTime frame
1. Cardiovascular mortality at 1 year following transcatheter aortic valve implantation 2. Need for permanent pacemaker implantation following transcatheter aortic valve implantation 3. Left ventricular ejection fraction at 30 days and at 1 year following transcatheter aortic valve implantation

Countries

United Kingdom

Contacts

Public ContactSatpal;Aung Arri;Myat

;

satpal.arri@gmail.com;aung.myat@nhs.net+44 (0)207 188 1008;+44 (0)207 188 1008

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 4, 2026