Clinical trial
Genotype/Phenotype Correlation of Movement Disorders and Other Neurological…
NCT00001667 · National Institute of Neurological Disorders and Stroke (NINDS), NIH · Completed
Key facts
| NCT number | NCT00001667 |
|---|---|
| Title | Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases |
| Official title | Genotype/Phenotype Correlation of Movement Disorders and Other Neurological Diseases |
| Lead sponsor | National Institute of Neurological Disorders and Stroke (NINDS), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Movement Disorders, Myoclonus, Nervous System Diseases, Tic Disorders, Tremor |
| Enrollment | 300 |
| Start date | Mar 1, 1997 |
| Completion | Apr 1, 2000 |
| First posted | Dec 10, 2002 |
| Last update posted | Mar 4, 2008 |
| Countries | United States |
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: