Functional Impairment in Albinism
Functional Impairment in Albinism
Recruiting · NCT06345976 · Registry updated 2025-02-13Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Functional Impairment in Albinism | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, eye disorder, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, metabolic disease, ocular albinism, skin disorder, skin pigmentation disorder | Recruiting | Not stated | 2025-02-13 | NCT06345976 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Fondation Ophtalmologique Adolphe de Rothschild | 81 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Hôpital Fondation A. de Rothschild | Paris | France | 11 |