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Can IV iron boost blood levels and daily energy for mothers before and after delivery?

NCT ID NCT07814378

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

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.

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.

Participants

About 800 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Oct 2026

An estimate. Start dates often move.

Expected to finish

Dec 2028

An estimate. End dates often move.

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.

Who is studied

anemia walk-in clinic

Ages

18 years and older

Sex

Female participants only

Healthy volunteers

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

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.

  1. The places running it

    2 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • University Hospital Frankfurt, Department for Anaesthesiolgy, Intensive Care, and Pain Therapy

    Frankfurt, Germany

  • University Hospital Würzburg, Department of Anaesthesiology, Intensive Care, Emergency and Pain Medicine

    Würzburg, Germany

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