Could iron pills make vaccines work better?
NCT ID NCT05919472
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study looked at whether giving oral iron supplements to iron-deficient women in Kenya before or at the same time as vaccination improves their immune response. 180 women received iron either before or with three vaccines (COVID-19, meningitis, and typhoid), or a placebo. The goal was to see if iron timing affects antibody levels. Results are not yet available, but the study aims to find a simple way to help vaccines work better in undernourished populations.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- oral iron supplements (ferrous sulfate)
- What this could lead to
- If it works, this could point toward a simple way to improve vaccine effectiveness in iron-deficient populations.
- What could go wrong
- This is a small, completed study focused on immune markers, not disease prevention. Results may not apply broadly or lead to immediate changes in practice.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
-
180 people
The number who actually took part.
- Started
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Jul 2023
- Finished
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Jul 2024
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 49 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Willing and able to give informed consent for participation in the trial * Female aged 18-49 years * Moderate anemia (Hb \<110 g/L, but not severely anemic with Hb \<80 g/L) • Iron deficient (ZnPP \>40 mmol/mol haem) * Anticipated residence in the study area for the study duration Exclusion Criteria: * Major chronic infectious disease (e.g., HIV infection); * Major chronic non-infectious disease (e.g., Type 2 diabetes, cancer); * Chronic medications; * Use of iron-containing mineral and vitamin supplementation 2 weeks prior to study start; * COVID-19 vaccine or confirmed COVID-19 infection within the past 2 years * MenACWY vaccine in the past * Typhoid vaccine in the past * Pregnant (confirmed by rapid test during screening) or lactating. * Malaria (confirmed by rapid test) à study start will be postponed
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Msambweni County Referral Hospital
Msambweni, 80404, Kenya
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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