SLC13A5 Deficiency Natural History Study - Remote Only
SLC13A5 Deficiency Natural History Study - Remote Only
Enrolling by invitation · NCT04681781 · Registry updated 2024-11-22Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| SLC13A5 Deficiency Natural History Study - Remote Only | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Disease Attributes, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Rare Diseases, amelocerebrohypohidrotic syndrome, brain disorder, central nervous system disorder, developmental and epileptic encephalopathy, 25, epilepsy, hereditary disease, movement disorder, nervous system disorder | Enrolling by invitation | Not stated | 2024-11-22 | NCT04681781 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Stanford University | 620 |
| TESS Research Foundation | 3 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Lucille Packard Children's Hospital, Stanford University | Palo Alto | United States | 2 |