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Iron Therapy in Erythropoietic Protoporphyria

Completed
Conditions
Erythropoietic Protoporphyria
Iron-deficiency
Registration Number
NCT05572125
Lead Sponsor
Bispebjerg Hospital
Brief Summary

Giving oral iron to patients with erythropoietic protoporphyria (EPP) who is iron deficient is thought to be beneficial. This is, however, not well documented. The purpose of this study is to investigate the effect and safety of oral iron in patients with EPP who is taking iron tablets due to iron deficiency.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
10
Inclusion Criteria
  • Diagnosed with EPP
  • Taking standard dose of iron tablets due to iron deficiency
Exclusion Criteria
  • Pregnant
  • Lactating

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change in erythrocyte protoporphyrin concentrationBefore treatment and after 6-8 weeks of treatment
Secondary Outcome Measures
NameTimeMethod
Change in hemoglobin and iron parametersBefore treatment and after 6-8 weeks of treatment
Adverse event6-8 weeks of treatment

Trial Locations

Locations (1)

Bispebjerg Hospital

🇩🇰

Copenhagen, Denmark

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