Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)
Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1)
Recruiting · NCT06593951 · Registry updated 2026-03-18Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Registry and Natural History Study for Progressive Myoclonus Epilepsy Type 1 (EPM1) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dyskinesias, Epilepsies, Myoclonic, Epilepsy, Generalized, Epileptic Syndromes, Myoclonus, Neurologic Manifestations, Pathological Conditions, Signs and Symptoms, Signs and Symptoms, Unverricht-Lundborg syndrome, brain disorder, central nervous system disorder, epilepsy, hereditary disease, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, progressive myoclonus epilepsy | Recruiting | Not stated | 2026-03-18 | NCT06593951 |
2 results · Page 1 of 1
Organizations
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| Organizations | Linked trials |
|---|---|
| Boston Children's Hospital | 238 |
| Epilepsy Foundation | 2 |
1 results · Page 1 of 1
Research sites
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| Research sites | City | Country | Linked trials |
|---|---|---|---|
| Boston Childrens Hospital | Boston | United States | 15 |