Clinical trial
SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic…
NCT00140829 · Institut National de la Santé Et de la Recherche Médicale, France, Other · Completed
Key facts
| NCT number | NCT00140829 |
|---|---|
| Title | SPATAX: Clinical and Genetic Analysis of Cerebellar Ataxias and Spastic Paraplegias |
| Official title | Clinical and Genetic Analysis of Autosomal Recessive Forms of Cerebellar Ataxias and Spastic Paraplegias |
| Acronym | Spatax |
| Lead sponsor | Institut National de la Santé Et de la Recherche Médicale, France, Other |
| Collaborators | Institut des Maladies Rares National Research Agency, France Paris Brain Institute (ICM) |
| Status | Completed |
| Study type | Observational |
| Conditions | Cerebellar Ataxias, Spastic Paraplegias |
| Enrollment | 6,000 |
| Start date | Feb 10, 2004 |
| Primary completion | Dec 1, 2020 |
| Completion | Dec 30, 2020 |
| First posted | Sep 1, 2005 |
| Last update posted | Feb 4, 2025 |
| Countries | Algeria, Belgium, Denmark, France, Israel, Italy, Lebanon, Morocco, Netherlands, Norway, Portugal, Saudi Arabia and 3 more |
At a glance
- 10–99 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: