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Medtronic Cardiac Surgery PMCF Registry

Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry

Who can join

All ages · All sexes

Inclusion Criteria:

1. Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
2. Patient has or is intended to receive or be treated with an eligible product
3. Patient is within enrollment window of treatment/therapy received at the time of their initial Registry enrollment, or meets criteria for retrospective enrollment

Exclusion Criteria:

1. Patient who is, or is expected to be, inaccessible for follow-up
2. Patient prohibited from participation by local law
3. Patient is currently enrolled in or plans to enroll in any concurrent investigational drug and/or device study that may confound results

About the study

This registry is being conducted to support ongoing post-market surveillance activities.

What is being tested

• Surgical Heart Valve Repair Products (device)
• Surgical Heart Valve Replacement Products (device)

Sponsor: Medtronic Cardiac Surgery · Participants: 2,700 · Started: Dec 2, 2019

Contact the study team

• Franceen Maroney · Phone: 1-800-328-2518
• Jessica Halverson · Phone: 1-800-328-2518

Official record on ClinicalTrials.gov — NCT04073420

Locations in the U.S.

Conditions

• Heart Valve Diseases

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.