Can IV iron boost blood levels and daily energy for mothers before and after delivery?
NCT ID NCT07814378
First seen Sep 11, 2026 · Last updated Sep 11, 2026
Summary
Anemia from iron deficiency is common in pregnancy and after childbirth, affecting many women. This trial tests whether iron given through a vein can raise hemoglobin levels and improve how women feel and function in everyday life before and after delivery. Researchers will compare blood measurements and quality-of-life reports in 800 pregnant women with iron deficiency. The study excludes women with certain blood disorders or other conditions that cause anemia.
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 supplementation
- What this could lead to
- If it works, intravenous iron could become a routine way to treat anemia in pregnancy and after birth, helping women feel stronger and function better during a demanding time.
- What could go wrong
- This is a large but still experimental comparison, and not every woman responds to iron the same way. Some may have side effects from the infusion, and the trial may not show a clear benefit for quality of life even if hemoglobin rises.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 800 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Oct 2026
An estimate. Start dates often move.
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- 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.
Who is studied
anemia walk-in clinic
- Ages
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18 years and older
- Sex
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Female participants only
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Pregnancy Exclusion Criteria: * Thalassemia * Sickle cell disease * Aplastic anemia * Hemochromatosis * Chronic inflammatory diseases associated with anemia of chronic disease * Severe renal insufficiency * Intravenous iron administration within 3 months prior to enrollment
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital Frankfurt, Department for Anaesthesiolgy, Intensive Care, and Pain Therapy
Frankfurt, Germany
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University Hospital Würzburg, Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine
Würzburg, Germany
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