Clinical trial
Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal…
NCT00136630 · Institut National de la Santé Et de la Recherche Médicale, France, Other · Completed
Key facts
| NCT number | NCT00136630 |
|---|---|
| Title | Natural History, Genetic Bases and Phenotype-genotype Correlations in Autosomal Dominant Spinocerebellar Degenerations |
| Official 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, Other |
| Collaborators | Assistance Publique - Hôpitaux de Paris |
| Status | Completed |
| Study type | Observational |
| Conditions | Spinocerebellar Ataxias, Spastic Paraplegias |
| Enrollment | 175 |
| Start date | May 1, 2005 |
| Primary completion | May 1, 2016 |
| Completion | May 1, 2020 |
| First posted | Aug 29, 2005 |
| Last update posted | Aug 25, 2021 |
| Countries | France |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: