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Clinical trial

Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations

NCT00136630 is registered in ClinicalTrials.gov with Institut National de la Santé Et de la Recherche Médicale, France as lead sponsor.

NCT NCT00136630
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Registry record

As filed in ClinicalTrials.gov.

Title
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations
Lead sponsor
Institut National de la Santé Et de la Recherche Médicale, France
Phase
Observational
Overall status
Completed
Start date
May 31, 2005
Completion date
May 31, 2020
Enrollment
175 (actual)
Sites
8

Conditions

As the registry lists them; a condition with its own page is linked.

spastic paraplegias, spinocerebellar ataxias