152
Participants
Start Date
June 2, 2022
Primary Completion Date
May 31, 2025
Study Completion Date
May 31, 2025
Ferrous fumarate
Patients randomized in the oral group, will all be prescribed ferrous fumarate 200 mg d.d. for the first 4 weeks. Then, depending on their iron status, 100 mg d.d. for the following 12 weeks or 4 more weeks 200 mg d.d. followed by 4 weeks 100 mg d.d.. If iron levels are still too low after 12 weeks, the intervention has failed.
MonoFer
Study patients will be treated with intravenous iron. The brand name of the iv iron is dependent on the hospital policy and the doses will be according to recommended guidelines (weight of patient). Iv iron is intramural medication without add-on status and needs infusion at daycare.
RECRUITING
Leiden University Medical Centre, Leiden
Collaborators (1)
University Medical Center Groningen
OTHER
UMC Utrecht
OTHER
Rijnstate Hospital
OTHER
Erasmus Medical Center
OTHER
Sint Franciscus Gasthuis
OTHER
Adrz, Goes
UNKNOWN
Medical Center Haaglanden
OTHER
Leiden University Medical Center
OTHER