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Sucrosomial Iron and Iron Sulphate to Blood Donors

Blood Donation Clinical Trial

Official title:
Randomized Open Comparative Trial of Oral Sucrosomial Iron (SiderAl Forte®) and Oral Iron Sulphate (Duroferon®) to Blood Donors.

Clinical Trial Summary

2 different oral iron supplementations after blood donation are compared.

Clinical Trial Description

Iron depletion is common in regular blood donors. During a blood donation the donor loses 200-250 mg iron. The routine at our donor sites is to give donors 20 tablets of iron sulphate (Duroferon®) 100 mg after blood donation. In this study we will compare two different iron supplementations given after blood donation. 60 donors are given oral sucrosomial Iron (SiderAl Forte®) and 60 donors are given oral iron sulphate (Duroferon®) after 4 successive blood donation. The primary purpose of this study is to compare the side effects of sucrosomial Iron and iron sulphate and to investigate if the iron balance can be maintained with sucrosomial iron. After each blood donation the donors are asked to answer a questionary with questions about side effects and symptoms of Restless legs syndrome/Willis-Ekbom (symptoms associated with iron deficiency). ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT05678647
Study type Interventional
Source Uppsala University Hospital
Contact Karin Schneider, MD
Phone +46186114159
Email Karin.Schneider@akademiska.se
Status Recruiting
Phase N/A
Start date January 31, 2023
Completion date January 1, 2025
View Details
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