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Direct Aortic vs Subclavian Access for TAVI: a Review of the Outcomes in the UK

Conditions
Aortic Stenosis
Registration Number
NCT02695147
Lead Sponsor
Royal Sussex County Hospital
Brief Summary

A retrospective analysis of outcomes of all patients who received TAVI via the subclavian or direct aortic approach between January 2011 and January 2016

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
400
Inclusion Criteria
  • Recieve TAVI via subclavian or direct aortic apporach in the UK
Exclusion Criteria
  • Nil

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
MACEUp to 5 years (average 3 years)
Secondary Outcome Measures
NameTimeMethod
Procedural Complications30 dyas post procedure

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