Clinical Trial

Measuring Iron Bioavailability From Oral Iron Supplements in Healthy Pre-menopausal Women Using Stable Isotopes

Study acronym: BOIs
Completed
View on ClinicalTrials.gov →
Summary
In this study the investigators will compare iron absorption from 3 doses of iron (5, 10, 15 mg, given as either Spatone™ or ferrous sulphate). Our primary objective is to determine iron absorption from each preparation by measuring stable isotope (57Fe) incorporation into haemoglobin.
Trial Details
NCT Number NCT07563686
Lead Sponsor King's College London
Conditions Iron Deficiency Anaemia Due to Dietary Causes
Enrollment 14 participants
Start Date 2024-01-13
Primary Completion 2025-03-31 (estimated)
Study Completion 2026-01-31 (estimated)
Updated on ClinicalTrials.gov 2026-05-04