A Randomized, Prospective, Double-Blind, Comparative Placebo-Controlled Study of Intravenous Iron Isomaltoside 1000 (Monofer®) administered by Infusions to Iron-Deficient Blood Donors

Mise à jour : Il y a 4 ans
Référence : EUCTR2012-001529-28

Femme Homme

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Extrait

The primary efficacy objective of the study is to evaluate the effect of IV iron isomaltoside 1000 compared with placebo in first-time female donors with p-ferritin below 60 µg/L. The safety objective of the study is to evaluate the safety of IV iron isomaltoside 1000 compared to placebo.


Critère d'inclusion

  • Female first-time bloddonors with iron deficiency

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