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Optimizing Dosing Strategies in Oral Iron Supplementation — OPTIDOSE  

Iron Deficiency Anemia Clinical Trial

Official title:
Optimizing Dosing Strategies in Oral Iron Supplementation

Clinical Trial Summary

The goal of this clinical trial is to evaluate, if a change in dosing strategy in oral iron supplementation from leads to an improvement of iron absorption and consequently a faster therapy in patients with iron deficiency anemia. The main question the study aims to answer is: Does a treatment effect (measured by change in hemoglobin after 12 weeks of treatment) exist between daily oral iron supplementation and interval administration (every second day)? Participants will receive oral iron supplementation every second day with double the standard dose (intervention group). Researchers will compare this group with the active control group, that receives oral iron supplementation every day with the standard dose. Participants will present for three patient visits (at baseline, after 6 and after 12 weeks of treatment).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT06238895
Study type Interventional
Source Luzerner Kantonsspital
Contact Meyer
Phone +41 41 205 11 11
Email eisenstudie@luks.ch
Status Recruiting
Phase Phase 4
Start date March 1, 2024
Completion date March 31, 2026
View Details
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