Hereditary, Spastic Paraplegia, Autosomal Dominant

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Review clinical trials related to Hereditary, Spastic Paraplegia, Autosomal Dominant. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

The preSPG4 Study - Studying the Prodromal and Early Phase of SPG4

Study goals 1. Prospective longitudinal data on progression in the natural course of SPG4 in presymptomatic mutation carriers prior to clinical disease onset and in early stages of disease 2. Biomarkers providing objective measures of disease activity

Participants needed: 200
Trial details
Age: 18-70Biological sex: AllType: InterventionalSponsor: University Hospital TuebingenUpdated: Aug 23, 2022Locations: 1
Eligibility criteria

First degree relatives (parents, offspring, and sibs) of SPG4 patients or sympto... [+2]

No known SPAST-mutation within the family [+2]