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

NCT ID: NCT02695147

Last Updated: 2016-03-01

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

UNKNOWN

Total Enrollment

400 participants

Study Classification

OBSERVATIONAL

Study Start Date

2016-02-29

Study Completion Date

2016-06-30

Brief Summary

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

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Detailed Description

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Conditions

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Aortic Stenosis

Study Design

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Observational Model Type

COHORT

Study Time Perspective

RETROSPECTIVE

Study Groups

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TAVI via Subclavian approach

Any TAVI procedure using any valve type performed via the subclavian approach

TAVI

Intervention Type PROCEDURE

TAVI via Direct Aortic approach

Any TAVI procedure using any valve type performed via the direct aortic approach

TAVI

Intervention Type PROCEDURE

Interventions

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TAVI

Intervention Type PROCEDURE

Eligibility Criteria

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Inclusion Criteria

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

Exclusion Criteria

* Nil
Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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National Institute for Cardiovascular Outcomes Research

OTHER

Sponsor Role collaborator

Royal Sussex County Hospital

OTHER

Sponsor Role lead

Responsible Party

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David Hildick-Smith

Consultant Cardiologist

Responsibility Role PRINCIPAL_INVESTIGATOR

Other Identifiers

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RoyalSussexTAVISCvsDA

Identifier Type: -

Identifier Source: org_study_id

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