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Intravenous iron in adults with cystic fibrosis


Therapeutic category
the type of treatment or therapy being studied. A therapy could range from a medication addressing a particular characteristic of CF to a device or activity e.g. exercise


Trial status

Closed to recruitment

Participating Centres
the different stages involved in the development of a new medication. Phase I focuses on initial safety in people. Phase 2 evaluates safety, correct dose and early signs of whether the medication works. Phase 3 is the stage before medication licensing and looks at safety and medication effectiveness. Phase 4 evaluates longer term use of a medication after it has been licensed for use

Phase IV

Full title

A pilot trial of intravenous iron for the treatment of iron deficiency in adult patients with cystic fibrosis

Adults with cystic fibrosis often have low iron levels (iron deficiency). This is partly due to poor absorption of iron from the gut, and partly to the trapping of iron within cells of the immune system during periods of infection. Unfortunately, iron tablets are often ineffective in this setting, and may cause significant side effects in patients with cystic fibrosis. In other patient groups, intravenous iron is used routinely to correct iron deficiency. In these patients it has been shown to be safe, and to improve energy levels, exercise tolerance, cognitive function and quality of life, even in the absence of anaemia. Recent research suggests that iron may be particularly beneficial in patients with heart and lung disease. Despite these possible benefits, IV iron is rarely used in patients with CF, due in part to concerns about encouraging the growth of bacterial in the lungs. Iron deficiency therefore often goes untreated. However, since no clinical trials have examined the use of IV iron in CF patients to date, the risks and benefits remain uncertain. We plan to undertake a small pilot study examining the effects of IV iron in 20 adults with CF and low iron levels. We will primarily assess whether intravenous iron is safe and effective at treating iron deficiency in this group, but will also study various other clinical parameters, to guide the design of future larger studies.

Trial Reference Number


Trial type


the name of the treatment or therapy being researched

Intravenous Iron

Recruitment target
the number of participants who need to be recruited for the trial in the UK


Last edited date

14 August 2018

CF sponsor

University of Oxford

CF sponsor type


Who can take part?



Top inclusion criteria
  • Age > = 18 years
  • Iron deficiency
Top exclusion criteria
  • Urgent need for iron supplementation (within 6 weeks of trial)
  • Active infection (currently requiring IV antibiotics)
  • Previous intravenous iron supplementation (within last 4 months)

CF centres running this trial


John Radcliffe Hospital


HeadingtonHeadley WayOxfordHeadley WayOxfordshire OX3 9DU



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