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Surgical Replacement and Transcatheter Aortic Valve Implantation Trial 10 Year Follow-up

Recruiting
Conditions
severe aortic valve stenosis
10046973
Registration Number
NL-OMON45149
Lead Sponsor
Medtronic B.V.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
160
Inclusion Criteria

All subjects currently enrolled in the randomized cohort of the SURTAVI trial
are eligible to consent to 10 year follow-up.

Exclusion Criteria

None

Study & Design

Study Type
Observational non invasive
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
<p>The primary objective of the 10 Year follow-up study is prospectively evaluate<br /><br>all-cause mortality or disabling stroke annually up to 10 years between TAVI<br /><br>(Transcatheter Aortic Valve Implantation) and SAVR (Surgical Aortic Valve<br /><br>Replacement).</p><br>
Secondary Outcome Measures
NameTimeMethod
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