Status:
COMPLETED
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
Collaborating Sponsors:
Assistance Publique - Hôpitaux de Paris
Conditions:
Spinocerebellar Ataxias
Spastic Paraplegias
Eligibility:
All Genders
18-80 years
Brief Summary
The autosomal dominant spinocerebellar degenerations are a highly heterogeneous, clinically and genetically, group of rare diseases and of severe evolution. So far, the responsible genes for less than...
Eligibility Criteria
Inclusion
- Progressive ataxia or paraplegia,
- Familial history of the disease (patients),
- Over 18 years of age
- No presentation of neurological or osteoarticular disorders
Exclusion
- Refusal to participate in the protocol,
- An unknown familial history,
- Presenting with an interrecurrent disorder making the evaluation of the disease (stroke, dementia) impossible
Key Trial Info
Start Date :
May 1 2005
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
May 1 2020
Estimated Enrollment :
175 Patients enrolled
Trial Details
Trial ID
NCT00136630
Start Date
May 1 2005
End Date
May 1 2020
Last Update
August 25 2021
Active Locations (8)
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1
Hôpital Pellegrin
Bordeaux, France, 33000
2
CHU de Grenoble
Grenoble, France, 38000
3
Hôpital Neurologique Pierre Wertheimer
Lyon, France, 69003
4
Hôpital La Timone
Marseille, France, 13005