Clinical Evaluation of Iron Treatment Efficiency Among Non-anemic But Iron-deficient Female Blood Donors
Status:
Completed
Trial end date:
2011-04-01
Target enrollment:
Participant gender:
Summary
The purpose of this study is to determine the subjective response of iron substitution
(Tardyferon®) on fatigue in women blood donors with a mean serum ferritin < 30ng/ml and to
assess variation of ferritin and hemoglobin after a blood donation.