Anemia Clinical Trial
Official title:
The Effect of Intra Venus Ferric Carboxymaltose Preoperative on Hemoglobin and Blood Transfusion Post Cardiac Surgery
Anemia after cardiac surgery is a vast phenomena. More than 70% of the patients who under
went surgery represented with hemoglobin less than 8 mg/dl (the cutoff for blood
transfusion) and more than 80% of the patients receives at least one unit of red blood cell
transfusion.
There were number of attempts to prevent the postoperative anemia by giving erythropoietin,
Iron per os and intra venus iron. non of the above have shown increase in Hemoglobin after
the cardiac surgery.
Research Objectives
The study objectives are:
1. Determine hemoglobin values in non-anemic patients given ferric Carboxymaltose prior to
and post heart surgery.
2. Determine the effect of ferric Carboxymaltose in non-anemic patients prior to surgery
on the number of blood units administer postoperation.
Research Methods Prospective, randomized, double-blind, placebo-controlled research. All
patients who are in the cardiac surgery department for bypass surgery, valve replacement
surgery or combined surgery will be eligible to participate in the study. The study will be
presented and explained to all patients and, if they consent, patients will be divided into
two random groups. One group will receive Ferinject IV 24-48 hours prior to surgery. The
second group will receive a placebo drug in the same time period as when the drug Ferinject
is administered.
The Population Studied All patients aged 18 or older hospitalized at the Rambam Medical
Center and are candidates for open-heart surgery (coronary artery bypass, valve, combined).
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment
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