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NCT04735848

Plasma Hepcidin Response to Differently Dosed Iron Supplements

Completed NA Last updated 8 October 2021
What this trial tests

NA trial testing Iron-supplement application in Iron Deficiency (Without Anemia) in 15 participants. Completed in 31 August 2021.

Timeline
1 June 2021
Primary endpoint
31 August 2021
31 August 2021

Quick facts

Lead sponsorPierre-Alexandre Krayenbuehl
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationnon randomized
Designcrossover
Maskingnone
Primary purposebasic science
Enrollment15
Start date1 June 2021
Primary completion31 August 2021
Estimated completion31 August 2021
Sites1 location across Switzerland

Drugs / interventions tested

Conditions studied

Sponsor

Pierre-Alexandre Krayenbuehl

Who can join

18 and older, female only, with Iron Deficiency (Without Anemia). Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The study participants will take 3 different doses of iron supplements at 8 am, on 3 different days. By taking blood samples in the morning and afternoon, the investigators will determine the effects of the iron supplements on plasma hepcidin and compare them to baseline plasma hepcidin values.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. The magnitude of the plasma hepcidin response to oral iron supplements depends on the iron dosage.
    Karczewski M, Simic S, Saleh L, Nowak A, et al · · 2024 · cited 1× · PMID 38579297 · DOI 10.57187/s.3635

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Other recruiting trials for Iron Deficiency (Without Anemia)

Currently open trials in the same condition.

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