Lutonix® Global AV Registry

Mise à jour : Il y a 5 ans
Référence : NCT02746159

Femme et Homme

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Extrait

The purpose of this Registry is to enroll patients presenting with clinical and hemodynamic abnormalities in native or synthetic (grafts) arteriovenous (AV) fistulae located in the arm. Subjects will be treated with the Lutonix DCB carrying the CE Mark per current IFU and followed clinically for a minimum of 12 months.


Critère d'inclusion

  • Arteriovenous Fistula

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