Anemia Clinical Trial
Official title:
Heme Iron Polypeptide for the Treatment of Iron Deficiency Anemia in Pre-Dialysis Patients: A Pilot Randomized Controlled Study
The purpose of this study is to determine if oral Heme Iron Polypeptide is as effective as intravenous (IV) iron sucrose in the treatment of iron-deficiency anemia for patients with chronic kidney disease.
Iron deficiency anemia is common in patients with pre-dialysis chronic kidney disease, and
is associated with significant morbidity. Conventional treatment with oral iron salts or IV
iron formulations are costly and are associated with side effects. Heme iron polypeptide is
a newly available formulation of oral iron which can be administered orally, is well
absorbed by uremic patients, and has potentially fewer side effects.
Comparison: Iron deficient anemic patients will be randomized to either oral heme iron
polypeptide or IV iron sucrose for six months.
;
Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator), Primary Purpose: Treatment
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