Iron boost after heart valve procedure shows promise in small trial
NCT ID NCT04206228
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.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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149 people
The number who actually took part.
- Started
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Jan 2020
- Finished
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Feb 2022
- 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 years and older
- Sex
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Anyone
- 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.
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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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Genom att skicka in godkänner du våra Användarvillkor
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.
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- A new heart valve without Open-Heart surgery: can it help High-Risk patients?
- Could a common blood pressure pill protect the heart after valve replacement?
- Iron infusions put to the test for heart failure stamina