Iron deficiency may blunt vaccine protection, study suggests
NCT ID NCT04915820
First seen Jun 26, 2026 · Last updated Jun 26, 2026
Summary
This study looked at whether iron deficiency anemia makes COVID-19 vaccines less effective in young women. Researchers gave intravenous iron to 121 participants and measured their immune responses. The goal was to see if correcting iron deficiency could boost vaccine protection.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- intravenous iron (ferric carboxymaltose)
- What this could lead to
- If iron deficiency is shown to weaken vaccine response, treating it could improve vaccine effectiveness in vulnerable populations.
- What could go wrong
- This is a small, completed observational study without a control group. Results may not apply broadly, and iron treatment carries rare risks like allergic reactions.
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
-
121 people
The number who actually took part.
- Started
-
May 2021
- Finished
-
Sep 2021
- Lead sponsor
-
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
-
18 to 55 years
- Sex
-
Female participants only
- Healthy volunteers
-
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: 18-55 years old Zinc protoporphyrin \> or equal 40 mmol/mol heme hemoglobin \< or equal 109 g/L no malaria no known HIV infection no medical condition that precludes study involvement no iron supplementation 1 week prior to study start no recent tuberculosis infection no vaccination of yellow fever or influenza prior to enrolment not pregnant Exclusion Criteria: \-
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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, Kwale County, Kenya
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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- Can starting iron sooner protect preterm babies on donor milk?
- When the immune system Can't fight back: tracking three respiratory viruses