Phase 2
N=149
Intravenous Iron Supplement for Iron Deficiency in Patients With Severe Aortic Stenosis
Severe Aortic Stenosis · Iron-deficiency
Bottom Line
View on ClinicalTrials.gov: NCT04206228 ↗Enrolled (actual)
149
Serious AEs
58.1%
Results posted
Apr 2026
Primary outcome: Primary: Submaximal Exercise Test — 375; 384 meters
Study Design & Population
- Study type
- Interventional
- Phase
- Phase 2
- Interventions
- Intravenous iron isomaltoside (Drug); Placebo (Drug)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Oslo University Hospital
- Primary completion
- Feb 2022
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Submaximal Exercise Test |
375; 384 | — |
| SECONDARY Iron Deficiency |
12; 46 | — |
| SECONDARY Muscle Strength |
28; 32 | — |
| SECONDARY The 36-item Short Health Survey Questionnaire (SF-36) Summary PCS |
45; 43 | — |
| SECONDARY The 3-level Version of EQ-5D (EQ-5D-3L) Questionnaire |
0.91; 0.91 | — |
| SECONDARY EuroQol-visual Analogue Scales (EQ-VAS) |
70; 75 | — |
| SECONDARY The Kansas City Cardiomyopathy Questionnaire (KCCQ) Overall Summary Score |
88; 82 | — |
| SECONDARY N-terminal Pro-B-type Natriuretic Peptide (NT-proBNP) |
611; 873 | — |
| SECONDARY Cardiac Troponin T (TnT) |
19; 22 | — |
| SECONDARY New York Heart Association Functional Class |
35; 30; 15; 20; 1; 3 | — |
Summary
Iron deficiency is a prevalent nutritional deficiency and a common cause of anemia. Although iron deficiency is traditionally linked to anemia, iron deficiency is prevalent even in the absence of anaemia and in itself limits function and survival. Iron deficiency is a common feature of various chronic diseases, and up to 50% of patients with heart failure have iron deficiency. Iron deficiency is more prevalent the more advanced the disease is and occurs more frequently in women. Iron deficiency comprises absolute iron deficiency (usually defined as ferritin < 100 ng/ml) as well as functional iron deficiency, in which iron supply is inadequate to meet the demand for the production of red blood cells and other cellular functions despite normal or abundant body iron stores. Iron deficiency is associated with poor exercise capacity, lethargy and reduced quality of life. Results from our studies have shown that iron deficiency is prevalent in patients with aortic stenosis. Some of the symptoms associated with aortic stenosis, such as fatigue, reduced exercise capacity, dyspnoea and cognitive dysfunction, have traditionally been thought to be caused by the haemodynamic derangements precipitated by the valvular stenosis. However, similar symptoms can be brought about by iron deficiency, and the investigators hypothesize that intravenous iron supplement will improve exercise capacity, muscle strength, cognition, health-related quality of life and myocardial function in patients with severe aortic stenosis and iron deficiency. This is a phase 2, double blind, randomised, placebo-controlled trial. Participants will be randomised in a 1:1 fashion to receive a single intravenous dose of iron isomaltoside (50 patients) or matching placebo (50 patients). The study is designed to show superiority with regard to the primary endpoint in patients assigned to active treatment versus patients allocated to the placebo arm. The main goal is to evaluate the effect of a single dose of intravenous iron isomaltoside on exercise capacity after transcatheter aortic valve implantation in patients with severe aortic stenosis and iron deficiency. For this study, the investigators have defined as serum ferritin < 100 µg/l or ferritin between 100 and 300 µg/l in combination with a transferrin saturation < 20 %.
Eligibility Criteria
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 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 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.
Data sourced from ClinicalTrials.gov (NCT04206228). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.