Study to evaluate the efficacy of intravenous iron supplementation in the prevention of anemia in patients receiving (neo)adjuvant breast cancer regimens.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
100
single dose of 200 mg (2 ampoules), 24-48 hours after administration of chemotherapy for a total of four doses
Instituto Do Cancer Do Estado de São Paulo
São Paulo, São Paulo, Brazil
RECRUITINGHospital Sirio Libanes
São Paulo, São Paulo, Brazil
RECRUITINGEvaluate the efficacy of intravenous iron supplementation in the prevention of anemia in patients receiving (neo)adjuvant breast cancer regimens
Anemia prevention defined by hemoglobin levels
Time frame: 18 weeks
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