Transcatheter aortic valve implantation (TAVi)

Medtronic real-world results

The CoreValve™/Evolut™ platform provides reproducible results from clinical trial to the real world.

Explore our STS/ACC TVT Registry™* data that supports the excellent clinical performance seen in our trials.

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FORWARD Study¹

This multicenter, prospective, single-arm, observational post-market study evaluated the safety and performance of the Evolut™ R system in a routine hospital setting.

Study Status/Duration: 12-month outcomes reported/3-year follow-up
Sample Size: N = 1040
Devices: Evolut™ R TAV

1 year hemodynamic data
Valve Performance

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30-day procedural outcomes
All Cause Rates

ADVANCE Study²

ADVANCE is a multicenter, prospective, single-arm, observational study to evaluate safety and performance of the CoreValve™ system in a routine clinical setting.

Study Status/Duration: 5-year outcomes reported/5-year follow-up
Sample Size: N = 1,015
Devices: CoreValve, TAV

SEE STUDY DATA

Graph showing effective orifice area and mean gradient over 5 years.
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Key Medtronic trials

Review the latest data supporting the Evolut™ platform.

Explore the data

Procedure and performance

Discover our procedural guidance and outcomes you can expect from the Evolut™ platform.

Explore the technique

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References

Harvey JE. Decreasing Permanent Pacemaker Implantation Rates in the STS/ACC TVT Registry with a Supra-annular Self-expanding Transcatheter Heart Valve. Presented at TVT2022; June 9, 2022; Chicago, IL.

Bajwa T, Rammohan C, Puri R, et al. The next-generation self-expanding transcatheter device: 30-day outcomes from the TVT-Registry. Presented at EuroPCR2021; May 2021.

DISCLAIMER

The material on this website should not be considered the exclusive source of information, it does not replace or supersede information contained in the device manual(s). Please note that the intended use of a product may vary depending on geographical approvals.

See the device manual(s) for detailed information regarding the intended use, the implant procedure, indications, contraindications, warnings, precautions, and potential adverse events.

For a MRI compatible device(s), consult the MRI information in the device manual(s) before performing a MRI. If a device is eligible for eIFU usage, instructions for use can be found at Medtronic’s website manuals.medtronic.com.

Manuals can be viewed using a current version of any major internet browser. For best results, use Adobe Acrobat® Reader with the browser.

Medtronic products placed on European markets bear the CE mark and the UKCA mark (if applicable). For any further information, contact your local Medtronic representative.

™*Third party brands are trademarks of their respective owners. All other brands are trademarks of a Medtronic company.