RecruitingNCT07798674
Rare condition
Infantile-onset ascending hereditary spastic paralysis
17
studies recruiting now
as of 7 Sept 2026
43
studies registered in total
as of 7 Sept 2026
10
countries with a recruiting site
as of 7 Sept 2026
1 Sept 2026
most recent study posted
among recruiting studies
Recruiting trials
RecruitingNot applicableNCT07417943
Neuromodulation to Enhance Motor Function in HSP
RecruitingPhase 3NCT06692712
Phase 3 Efficacy Study With Concurrent Control of IT MELPIDA in SPG50.Concurrent Controls.
RecruitingNCT06572046
STOP-HSP.Net: a Registry for Hereditary Spastic Paraplegia as an Integration Tool for Future Therapeutic Strategies
RecruitingNCT05354622
Hereditary Spastic Paraplegia Genomic Sequencing Initiative (HSPseq)
Showing the 5 most recently updated recruiting studies, as recorded 7 Sept 2026. Live status on each study page.
See all 17 recruiting studiesWhere recruiting studies are running
Countries with at least one recruiting site among the studies above, 7 Sept 2026. Tap a country to search trials there.
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Patient organisations
We do not yet list a dedicated organisation for this condition. The directories below are the best route.
About Infantile-onset ascending hereditary spastic paralysis
RareTrial does not yet hold a plain-language description of this condition. The most reliable starting point is Orphanet’s expert page, which lists specialist centres, registries and patient organisations, and the gene involved (ALS2).
Related conditions
Information, not medical advice. Trial listings are shown as recorded on ClinicalTrials.gov; whether any study is right for you is a decision for you and your clinicians, and eligibility is decided by each research team. Disease information from Orphanet (CC BY 4.0).