Hereditary Autosomal Dominant Spastic Paraplegia
Hereditary Autosomal Dominant Spastic Paraplegia
Explore linked clinical trials. Standard reference: MESH:M03367341 results ยท Page 1 of 1
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| The preSPG4 Study - Studying the Prodromal and Early Phase of SPG4 | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hereditary Autosomal Dominant Spastic Paraplegia, central nervous system malformation, hereditary disease, hereditary motor and sensory neuropathy, hereditary spastic paraplegia, inherited neurodegenerative disorder, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, polyneuropathy | Recruiting | Not applicable | 2022-08-23 | NCT03206190 |