Medtronic Cardiac Device Registry - Clinical Trial

What is the 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.

What is the Condition Being Studied?

Heart Disease

Who Can Participate in the Study?

Adults who have or will be treated with a Medtronic heart device.

Age Group
Adults

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.

Study Details

Full Title
Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry Base Protocol
Principal Investigator
Protocol Number
IRB: PRO00104466
Phase
Phase N/A
Enrollment Status
Open for Enrollment
Participate
Contact the Duke Recruitment Innovation Center
MyResearchPartners@duke.edu
or
919-681-5698