Medtronic Cardiac Device Registry - Clinical Trial

Email to Participate

¿Cuál es el Propósito de este estudio?

We are doing this study to learn more about the safety and performance of heart valve repair and replacement products made by Medtronic.

¿Cuál es la Condición que se está estudiando?

Enfermedad cardíaca

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

Grupo etario

Adultos

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.

Título Completo

Medtronic Cardiac Surgery Post Market Clinical Follow-up Registry Base Protocol

Investigador Principal

Brittany Anne Zwischenberger, MD

Especialista en cirugía cardíaca

Número de Protocolo

IRB: PRO00104466

Fase

Fase N/A

Estado de inscripción

Abierto para inscripción

Participate

Email hillary.hood@duke.edu

O bien,

919-681-5698