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Iron Supplementation in Upper Non-variceal Gastrointestinal Bleeding
Sponsor: University of Pecs
Summary
Anemia is a frequent complication of gastrointestinal bleeding, affecting 61% of the patients. Currently, anemia caused by gastrointestinal bleeding can be treated with iron supplementation. However, the dose and route of the administration are still a question. The FIERCE clinical trial aims to compare the effect of intravenous iron supplementation and oral iron replacement on mortality, unplanned emergency visits, and hospital readmissions in multimorbid patients with acute nonvariceal gastrointestinal bleeding.
Official title: Intravenous Ferric Carboxymaltose Versus Oral Ferrous Sulfate Replacement in Anaemia Due to Acute Nonvariceal Gastrointestinal Bleeding (FIERCE): Protocol of a Multicentre Randomised Controlled Trial
Key Details
Gender
All
Age Range
65 Years - Any
Study Type
INTERVENTIONAL
Enrollment
570
Start Date
2025-09-01
Completion Date
2028-02-01
Last Updated
2025-03-30
Healthy Volunteers
No
Conditions
Interventions
Oral iron supplementation
Ca. 200-300 mg of ferrous sulfate will be administered orally every day for 3 months.
Intravenous iron supplementation
One dose of intravenous 1000 mg ferric carboxymaltose will be administered on the day of randomization.
Locations (1)
Institute for Translational Medicine, University of Pécs
Pécs, Hungary