Peripheral Serotonin and Albinism
Peripheral Serotonin and Albinism
Recruiting · NCT06138509 · Registry updated 2025-09-12Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Peripheral Serotonin and Albinism | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Hemic and Lymphatic Diseases, Iron Deficiencies, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, anemia, eye disorder, hematologic disorder, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, iron metabolism disease, metabolic disease, oculocutaneous albinism, skin disorder, skin pigmentation disorder | Recruiting | Not stated | 2025-09-12 | NCT06138509 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Assistance Publique - Hôpitaux de Paris | 985 |
| URC-CIC Paris Descartes Necker Cochin | 154 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Hôpital Necker-Enfants Malades | Paris | France | 35 |