Hepcidin After Intravenous Iron Treatment

NCT06264687 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 10

Last updated 2024-02-20

No results posted yet for this study

Summary

The aim of this study is to investigate the hepcidin hormone response after intravenous iron administration.

Conditions

  • Iron Deficiency (Without Anemia)

Sponsors & Collaborators

  • Pierre-Alexandre Krayenbühl

    lead OTHER

Eligibility

Min Age
18 Years
Max Age
50 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-03-01
Primary Completion
2024-05-31
Completion
2024-05-31

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06264687 on ClinicalTrials.gov