Iron Therapy in Erythropoietic Protoporphyria
Completed
- Conditions
- Erythropoietic ProtoporphyriaIron-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
Name Time Method Change in erythrocyte protoporphyrin concentration Before treatment and after 6-8 weeks of treatment
- Secondary Outcome Measures
Name Time Method Change in hemoglobin and iron parameters Before treatment and after 6-8 weeks of treatment Adverse event 6-8 weeks of treatment
Trial Locations
- Locations (1)
Bispebjerg Hospital
🇩🇰Copenhagen, Denmark