Clinical Trials Directory

Trials / Completed

CompletedNCT02175888

The Optimization of Bioavailability From Iron Supplements: Study 1

The Optimization of Bioavailability From Iron Supplements: Examinations of Different Supplementation Regimens Including Hepcidin Profiles

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
20 (actual)
Sponsor
Swiss Federal Institute of Technology · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Iron deficiency (ID) with or without anaemia (IDA) is a major public health problem worldwide, especially in women of reproductive age and young children. Iron supplementation is an effective strategy to prevent and treat ID and IDA. There is a lack of data on iron bioavailability from different supplementation regimens and how to optimize bioavailability in a cost-effective and patient-friendly way. The present study will test whether the fractional and total iron absorption from iron supplements (60 mg) administered daily for 14 days differs from that of iron supplements (60 mg) administered every second day for 28 days. The prevailing serum hepcidin concentration (SHep) is the major determinant of iron absorption and erythrocyte iron utilization. Therefore we will monitor SHep during the whole supplementation period. We hypothesize that the fractional and total iron absorption from the daily administration of 60 mg is lower than that from the administration on every second day due to increased SHep levels when supplements are administered daily. The study will provide important insights about the optimization of iron bioavailability from different supplementation regimens including the performance of SHep, a key regulator of human iron metabolism.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTDaily administration of 60 mg iron in form of ferrous sulphate capsules for 14 consecutive days
DIETARY_SUPPLEMENTAdministrations of 60 mg iron in form of ferrous sulphate capsules on every second day for 28 days

Timeline

Start date
2015-10-01
Primary completion
2015-12-01
Completion
2016-01-01
First posted
2014-06-26
Last updated
2017-11-07

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT02175888. Inclusion in this directory is not an endorsement.