Purpose of this Study
We are doing this study to learn more about the safety and performance of heart valve repair and replacement products made by Medtronic.
Who Can Participate?
Eligibility
Adults who have or will be treated with a Medtronic heart device.
What is Involved?
If you agree to be in this study we will collect information about your heart condition and surgery from your medical records.
This information will be collected before your surgery through 10 years after your surgery.
This information will be collected before your surgery through 10 years after your surgery.
Study Details
Full Title
Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry Base Protocol
Principal Investigator
Donald
Glower
Protocol Number
PRO00104466
Phase
N/A
Enrollment Status
OPEN TO ACCRUAL