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Imaging Intravenous Iron

Sponsor: University of Oxford

NCT ID: NCT05609318

View on ClinicalTrials.gov ↗

At a glance

What the study gets you
Health checks and monitoring — no treatment given
Type of study
Observational (no treatment given)
Time in hospital
In-person visits at study sites — visit count not specified by the sponsor
Drug or intervention
Not specified by the sponsor
How long the study runs
Study runs about 50 months (dates as stated)
About the drug or intervention
Not specified by the sponsor
Patient visit burden
Not specified by the sponsor
Type of study
Observing health over time
Ages
18 Years and over
Who
All
Number of participants
12
Started
2022-10-29
Last checked
2026-05

Plain English Summary

What is this study?

  • • Testing a new treatment for iron-deficiency
  • • Clinical study - 12 participants
  • • The aim of this study is to track where the iron goes in different tissues in the hours, days and weeks after an intravenous iron infusion

Who can take part?

  • • Ages 18 Years and over
  • • Diagnosed with iron-deficiency

Where?

  • • Oxford - Oxford Centre for Clinical Magnetic Resonance Research (OCMR)

This is a simplified summary. Always discuss with your doctor before making any decisions.

About This Trial

The aim of this study is to track where the iron goes in different tissues in the hours, days and weeks after an intravenous iron infusion. We will track iron in tissues using MRI relaxometry parameters R1/R2/R2\* which are well established as accurate indicators of tissue iron content.

More detail

This is a prospective, observational, study exploring the kinetics of tissue iron uptake following intravenous iron infusion (Ferinject), received as part of standard clinical care in a group of iron-deficient patients. Participants will be recruited through the Iron Deficiency Management Service, part of the Oxford University Hospitals NHS Foundation Trust (OUHFT) . Participants will receive their intravenous iron infusion (Ferinject) as part of their standard clinical care by an NHS clinician. They will undergo all the study MRI scans and additional study procedures at the Oxford Centre for Clinical Magnetic Resonance Research (OCMR), which is based at the John Radcliffe Hospital and is part of the Division of Cardiovascular Medicine within the Radcliffe Department of Medicine at the University of Oxford. Each participant will undergo 4 MRI scans; baseline, 3hours, 14 days and 42 days post intravenous iron infusion. Blood samples will also be collected at those timepoints for assessment of relevant heamatological and iron parameters.

Iron-deficiency

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What we know so far

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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.

Eligibility at a Glance

Key info

  • Age: 18 Years and over
  • Who can join: All genders

What the study is looking for

  • ✓Participant is willing and able to give agreement to take part for participation in the study.
  • ✓Aged 18 years or above.
  • ✓Anaemia (haemoglobin less than 120g/L for women and less than 130g/L for men) and/or confirmed iron deficiency...
  • ✓Scheduled to receive intravenous iron for correction of iron deficiency.

Who cannot take part

  • ✗Any MRI incompatible implants (e.g. heart, neuro, ocular implants, surgical clips, aneurysm clips, shrapnel/bullets)
  • ✗Pregnant or lactating participant
  • ✗Acute decompensated heart failure
  • ✗Unstable clinical status
  • ✗Any other medical conditions which would influence the reliability of the study results determined by the investigators.
See the full criteria
Inclusion Criteria: * Participant is willing and able to give informed consent for participation in the study. * Aged 18 years or above. * Anaemia (haemoglobin less than 120g/L for women and less than 130g/L for men) and/or confirmed iron deficiency (ferritin less than 100mcg/L and/or transferrin saturation less than 20%). * Scheduled to receive intravenous iron for correction of iron deficiency. Exclusion Criteria: * Any MRI incompatible implants (e.g. cardiac, neuro, ocular implants, surgical clips, aneurysm clips, shrapnel/bullets) * Pregnant or lactating participant * Acute decompensated heart failure * Unstable clinical status * Any other medical conditions which would influence the reliability of the study results determined by the investigators. * Any other contraindication to MRI to be confirmed by the qualified MRI operator, e.g. tattoos containing traces of metal.

Where Is This Study? (1 UK site)

Oxford Centre for Clinical Magnetic Resonance Research (OCMR)

Oxford OX3 9DU, United Kingdom

Recruiting
Site contact (verified)
Data sourced from ClinicalTrials.gov · Last verified: 2026-05