Clinical Trials Directory

Trials / Completed

CompletedNCT05105438

Alternate Day vs. Daily Iron Supplementation in Iron Depleted Women

Comparing Oral Iron Supplementation Using Alternate-day Dosing to the Standard of Care Consecutive-day Dosing in Iron-depleted Women With or Without Mild Anemia

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
150 (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 anemia is a major public health problem worldwide, especially in women of reproductive age. Iron supplementation can be an effective strategy to prevent and treat ID and iron deficiency anemia (IDA). Recent studies suggests that giving oral iron every other day would be an optimized dosing regimen with maximized absorption and a lower incidence of gastrointestinal side effects compared to consecutive day dosing. Long-term trials in which participants and investigators are blinded to the dosing interval with iron status and gastrointestinal side effects as study outcomes are needed.

Conditions

Interventions

TypeNameDescription
DIETARY_SUPPLEMENTConsecutive Day Dosing100 mg iron as FeSO4 daily for 3 months, followed by matched placebo daily for 3 months.
DIETARY_SUPPLEMENTAlternate Day Dosing100 mg iron as FeSO4 and matched placebo on alternating days for 6 months.

Timeline

Start date
2021-12-16
Primary completion
2022-08-10
Completion
2022-12-08
First posted
2021-11-03
Last updated
2024-01-24

Locations

1 site across 1 country: Switzerland

Source: ClinicalTrials.gov record NCT05105438. Inclusion in this directory is not an endorsement.