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Phase 2 N=149 Randomized Triple-blind Treatment

Intravenous Iron Supplement for Iron Deficiency in Patients With Severe Aortic Stenosis

Severe Aortic Stenosis · Iron-deficiency

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

OutcomeResultp-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.
View full record on ClinicalTrials.gov →

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.

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