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Clinical Trial Summary

Hypophosphatemia induced by treatments with injectable iron is a frequent side effect already reported during marketing. Situations of osteomalacia secondary to these hypophosphatemias are rarer and reported in the form of case reports in the literature. Hypophosphatemia in this context is attributed to an excess of FGF-23 (defect of degradation linked to carbohydrates in martial preparations) with renal leakage of phosphate. Rendu-Osler disease (ROM) is an autosomal dominant genetic disease, favoring the formation of vascular malformations, including nasal and digestive telangiectasias causing repeated bleeding, even hemorrhages. Iron deficiency is frequent and profound there, and oral martial treatments are often insufficient to compensate for these losses. Regular iron infusions, to avoid transfusions, are often necessary.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms

  • Telangiectasia, Hereditary Hemorrhagic

NCT number NCT05544669
Study type Observational
Source University Hospital, Strasbourg, France
Contact Murielle RONDEAU-LUTZ, MD
Phone 33 3 69 55 10 13
Email murielle.rondeau-lutz@chru-strasbourg.fr
Status Recruiting
Phase
Start date August 1, 2022
Completion date July 21, 2024