Circadian Variation of Urinary Copper Excretion in Wilson Disease Patients
Circadian Variation of Urinary Copper Excretion in Wilson Disease Patients
Recruiting · NCT06430359 · Registry updated 2026-01-15Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Circadian Variation of Urinary Copper Excretion in Wilson Disease Patients | Brain Diseases, Metabolic, Brain Diseases, Metabolic, Inborn, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Digestive System Diseases, Nutritional and Metabolic Diseases, Wilson disease, basal ganglia disorder, brain disorder, central nervous system disorder, hereditary disease, inborn errors of metabolism, inborn metal metabolism disorder, inherited neurodegenerative disorder, liver disorder, metabolic disease, movement disorder, nervous system disorder, neurodegenerative disease | Recruiting | Not stated | 2026-01-15 | NCT06430359 |
1 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Hospices Civils de Lyon | 429 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Service de Gastroentérologie, Hépatologie et Nutrition Pédiatriques - Hôpital Femme Mère Enfant | Bron | France | 1 |