Clinical trial
Genetic Analysis of the Chiari I Malformation
NCT00004738 · National Institute of Neurological Disorders and Stroke (NINDS), NIH · Completed
Key facts
| NCT number | NCT00004738 |
|---|---|
| Title | Genetic Analysis of the Chiari I Malformation |
| Official title | Genetic Analysis of the Chiari I Malformation |
| Lead sponsor | National Institute of Neurological Disorders and Stroke (NINDS), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Syringomyelia, Type I Arnold Chiari Malformation |
| Enrollment | 152 |
| Start date | Jun 4, 2001 |
| First posted | Feb 28, 2000 |
| Last update posted | Jan 26, 2026 |
| Countries | Russia, 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: