IRONHEART: Intravenous Iron in Non-ischaemic Heart Failure

Recruiting Observational Study
Heart Failure Iron Deficiencies
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 and older
Sex
Any
Study type
Observational
Participants needed
16 (estimated)
Sponsor
University Hospital Southampton NHS Foundation Trust · Other
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About This Trial
The aim of this study is to observe the effect of intravenous ferric derisomaltose in participants with non-ischaemic heart failure (LVEF\<40%), iron deficiency (TSATS\<20%) and established on heart failure therapy including Sodium-glucose cotransporter 2 inhibitors (SGLT2i). Participants will undergo baseline laboratory blood tests, cardiac magnetic resonance imaging (cMRI), six-minute walk test,…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Participants capable of giving informed consent. * Aged 18yrs and above. * Diagnosed with heart failure and a reduction of their ejection fraction \< 40% by any modality. * Non ischaemic cardiomyopathy as determined by baseline cardiac magnetic resonance imaging. * Iron defici…
Contacts

Flett

+442381205906

andrew.flett@uhs.nhs.uk

CONTACT

Rachael Pulham

+442381205044

sponsor@uhs.nhs.uk

CONTACT