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

• Conditions: Aortic Stenosis
• Interventions: Procedure: TAVI

• 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

Study Timeline

• Status Verified: 2016-02
• Study Start: 2016-02
• Study First Submitted: 2016-02-24
• Study First Submitted QC: 2016-02-24
• Last Update Submitted: 2016-02-24
• Study First Posted: 2016-03-01
• Last Update Posted: 2016-03-01
• Primary Completion: 2016-06
• Study Completion: 2016-06

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

Arm && Interventions

Group	Intervention	Description
TAVI via Subclavian approach	TAVI	Any TAVI procedure using any valve type performed via the subclavian approach
TAVI via Direct Aortic approach	TAVI	Any TAVI procedure using any valve type performed via the direct aortic approach

Primary Outcome Measures

Name	Time	Method
MACE	Up to 5 years (average 3 years)

Secondary Outcome Measures

Name	Time	Method
Procedural Complications	30 dyas post procedure