Safety of Primovist / Eovist in Renally Impaired patients

Mise à jour : Il y a 4 ans
Référence : EUCTR2008-005867-33

Femme et Homme

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Extrait

The primary objective is to assess the magnitude of potential risk of developing NSF with the administration of Primovist/Eovist in patients with moderate to severe renal impairment for the development of NSF, based on diagnostically specific clinical and histopathological information.


Critère d'inclusion

  • Patients with moderate (eGFR 30 – 59 mL/min/1.73 m2) to severe renal impairment (eGFR < 30 mL/min/1.73 m2) scheduled to undergo contrast-enhanced MRI with Primovist/Eovist