Resumen

The purpose of the Registry is to provide continuing evaluation and periodic reporting of safety and effectiveness of Medtronic market-released products. The Registry data is intended to benefit and support interests of patients, hospitals, clinicians, regulatory bodies, payers, and industry by streamlining the clinical surveillance process and facilitating leading edge performance assessment via the least burdensome approach.

Elegibilidad

Sexo: ALL

Criterios de inclusión

Patient or legally authorized representative provides written authorization and/or consent per institution and geographical requirements
Patient has or is intended to receive or be treated with an eligible Medtronic product
Patient within enrollment window relative to therapy initiation or meets criteria for retrospective enrollment

Criterios de exclusión

Patient who is, or will be, inaccessible for follow-up
Patient is currently enrolled in or plans to enroll in any concurrent drug and/or device study that may confound results

Ubicaciones

Buenos Aires, Argentina

RECRUITING

Patrocinadores

PrincipalMedtronic

Contactos

Medtronic Product Surveillance Registry

CONTACT

rs.productsurveillanceregistry@medtronic.com