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Invent The Future - UC Davis Health System

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TAVI<br />

Trans<br />

femoral<br />

High Risk TF<br />

1:1 Randomization<br />

VS<br />

PARTNER Study Design<br />

ASSESSMENT:<br />

Transfemoral Access<br />

Surgical<br />

AVR<br />

Symptomatic Severe Aortic Stenosis<br />

TAVI<br />

Trans<br />

femoral<br />

ASSESSMENT: High Risk AVR Candidate<br />

3105 Total Patients Screened<br />

High Risk TA<br />

1:1 Randomization<br />

Surgical<br />

AVR<br />

Primary Endpoint: All Cause Mortality<br />

(1 yr) (Non-inferiority)<br />

VS<br />

Total = 1058 patients<br />

n= 700 High Risk 2 Parallel Trials:<br />

Inoperable n=358<br />

Individually Powered<br />

TAVI<br />

Trans<br />

femoral<br />

1:1 Randomization<br />

VS<br />

ASSESSMENT:<br />

Transfemoral Access<br />

Standard<br />

<strong>The</strong>rapy<br />

(usually BAV)<br />

Not In Study<br />

Primary Endpoint: All Cause Mortality<br />

over length of trial (Superiority)

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