The primary purpose of this study is to evaluate the safety and efficacy of preoperative intravenous ferric carboxymaltose in patients with anemia undergoing hip or knee replacement
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
3
iv administration of max. 50 ml (Dilution: 20 ml in 30 ml NaCl 0.9%) in 30 minutes
iv administration of max. 50 ml in 30 minutes
Charité Universitätsmedizin Berlin
Berlin, Germany
University Hospital Muenster
Münster, Germany
Number of RBC units
Time frame: Until postoperative day 7
Blood transfusion rate
Number of patients with blood transfusions
Time frame: Until postoperative day 7
Frequency of postoperative complications
Number of postoperative complications from baseline until postoperative day 7
Time frame: Until postoperative day 7
Frequency of postoperative complications
Number of postoperative complication from baseline until 6 weeks after surgical intervention
Time frame: Until 6 weeks after surgical intervention
Length of hospital stay
Time frame: 6 weeks after surgical intervention
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