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OpenTrials
Completed

NCT Number: NCT05572125

Iron Therapy in Erythropoietic Protoporphyria

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.

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Key information

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosed with EPP
  • Taking standard dose of iron tablets due to iron deficiency

Exclusion criteria

  • Pregnant
  • Lactating

Treatment and study plan

Primary outcomes

  1. Change in erythrocyte protoporphyrin concentration

    Time frame: Before treatment and after 6-8 weeks of treatment

Secondary outcomes

  1. Change in hemoglobin and iron parameters

    Time frame: Before treatment and after 6-8 weeks of treatment

  2. Adverse event

    Time frame: 6-8 weeks of treatment

Sponsors and collaborators

Lead sponsor

Bispebjerg Hospital

Other

Collaborators

  • Alfred Benzon Foundation

Registry information

Official study title

Oral Iron Therapy in Erythropoietic Protoporphyria

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Oct 7, 2022
Registry last updated
Feb 23, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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