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Iron boost after heart valve procedure shows promise in small trial

NCT ID NCT04206228

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looked at whether a single intravenous iron dose could improve exercise capacity in people with severe aortic stenosis and iron deficiency who were scheduled for a valve replacement. About 100 participants received either iron or a placebo. The main goal was to see if the iron group could walk farther on a 6-minute walk test 6 months later.

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

Phase 2

Tests whether the treatment actually works, and watches for side effects, in a larger group.

Participants

149 people

The number who actually took part.

Started

Jan 2020

Finished

Feb 2022

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 years and older

Sex

Anyone

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: * Aortic stenosis patients with peak flow velocity (\>3.5 m/s) scheduled for aortic valve replacement with TAVI * Iron deficiency defined as serum ferritin \< 100 µg/l or ferritin between 100 and 300 µg/l in combination with a transferrin saturation \< 20 %. * Age \> 18 years. * Signed informed consent and expected compliance with protocol. Exclusion Criteria: Patients will be excluded from the study if they meet any of the following criteria: * Anaemia (Haemoglobin \< 100 mg/l) * Haemochromatosis * Haemosiderosis * Porphyria cutanea tarda * Blood dyscrasias or any disorders causing haemolysis or unstable red blood cells * Decompensated liver disease (Child-Pugh score 7 or higher) * End-stage renal failure, i.e. eGFR \< 15 ml/min or on renal replacement therapy * Planned major surgery within 6 months * Unresolved cancer predisposing to chronic bleeding or associated with life expectancy \< 2 years * On erythropoietin analogues * Known sensitivity or intolerance to iron isomaltoside or other parenteral iron preparations * Intravenous iron supplement within 6 months prior to inclusion * A clear indication for intravenous iron supplement * On oral iron substitution (unless the subject agrees to stop treatment prior to randomisation) * Alcohol or drug abuse within 3 months of informed consent that would interfere with trial participation or any ongoing condition leading to decreased compliance with study procedures or study drug intake * Intake of an investigational drug in another trial within 30 days prior to intake of study medication in this trial or participating in another trial involving an investigational drug and/or follow-up * Failure to obtain written informed consent * Inability to walk at least 100 meters over 6 minutes * Women of child-bearing potential (1) 1. A woman is considered of childbearing potential, i.e. fertile, following menarche and until becoming post-menopausal unless permanently sterile. Permanent sterilisation methods include hysterectomy, bilateral salpingectomy and bilateral oophorectomy. Menopause is defined as 12 months continuous amenorrhea without an alternative medical cause in a female ≥ 55 years old or 12 months of spontaneous and continuous amenorrhea with a follicle stimulating hormone (FSH) level \> 40 IU/L (or according to the definition of "postmenopausal range" for the laboratory involved) in a female \< 55 years old unless the subject has undergone bilateral oophorectomy.

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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

  • Rikshospitalet University Hospital

    Oslo, Norway

More trials for these conditions

Other studies related to the condition(s) this trial covers.