Tundra Space

Tundra Space

Clinical Research Directory

Browse clinical research sites, groups, and studies.

Back to Studies
NOT YET RECRUITING
NCT05060731
PHASE4

Iron Supplementation in Upper Non-variceal Gastrointestinal Bleeding

Sponsor: University of Pecs

View on ClinicalTrials.gov

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

Interventions

DRUG

Oral iron supplementation

Ca. 200-300 mg of ferrous sulfate will be administered orally every day for 3 months.

DRUG

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