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Spastic paraplegia 3, autosomal dominant

Clinical trial condition

Spastic paraplegia 3, autosomal dominant

Explore clinical trials studying Spastic paraplegia 3, autosomal dominant. Study availability and eligibility vary by location and protocol.

3 public trials 2 recruiting studies

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Spastic paraplegia 3, autosomal dominant trial results

Recruiting

Registry and Natural History Study for Early Onset Hereditary Spastic Paraplegia

NCT04712812

Conditions: AP4-related Hereditary Spastic Paraplegia, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +26 more
Locations: Boston Children's Hospital Boston, Massachusetts, United States

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Recruiting

Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq)

NCT05354622

Conditions: Central Nervous System Diseases, Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, +27 more
Locations: Boston Children's Hospital Boston, Massachusetts, United States

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Completed

Improving Gait Adaptability in Hereditary Spastic Paraplegia

NCT04180098

Conditions: Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Genetic Diseases, Inborn, +12 more
Locations: Radboud universitair medisch centrum Nijmegen, Netherlands

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