Intravenous Iron in Adults With Cystic Fibrosis

Status Completed

Clinical Trial Summary

This pilot interventional cohort study will examine the effects of intravenous iron in adults with cystic fibrosis and iron deficiency.

Clinical Trial Description

Iron deficiency is common in adults with cystic fibrosis, and is associated with adverse outcomes. Oral iron supplementation is poorly tolerated and may be ineffective. In some centres, intravenous iron is used to correct iron deficiency, but concerns have been raised about the safety of this treatment in the setting of chronic airways infection. The investigators are therefore planning a pilot interventional cohort study examining the effects of intravenous iron in a group of adults with cystic fibrosis. Patients will be recruited in Oxford and studied prospectively over 16 weeks, with iron given at week 4. The primary focus of this single-centre pilot/feasibility study is safety, specifically in relation to infection. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT03632525
Study type	Interventional
Source	University of Oxford
Contact
Status	Completed
Phase	Phase 4
Start date	February 22, 2019
Completion date	October 26, 2021

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