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

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

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02695147
Enrollment
400
Registered
2016-03-01
Start date
2016-02-29
Completion date
2016-06-30
Last updated
2016-03-01

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

Conditions

Aortic Stenosis

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

Interventions

PROCEDURETAVI

Sponsors

National Institute for Cardiovascular Outcomes Research
CollaboratorOTHER
Royal Sussex County Hospital
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Recieve TAVI via subclavian or direct aortic apporach in the UK

Exclusion criteria

* Nil

Design outcomes

Primary

MeasureTime frame
MACEUp to 5 years (average 3 years)

Secondary

MeasureTime frame
Procedural Complications30 dyas post procedure

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026