Clinical trial
Phenotype/Genotype Correlations in Neuromuscular Disorders
NCT00017745 · National Institute of Neurological Disorders and Stroke (NINDS), NIH · Completed
Key facts
| NCT number | NCT00017745 |
|---|---|
| Title | Phenotype/Genotype Correlations in Neuromuscular Disorders |
| Official title | Phenotype/Genotype Correlations in Inherited Myopathies |
| Lead sponsor | National Institute of Neurological Disorders and Stroke (NINDS), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Neuromuscular Disease |
| Enrollment | 1,000 |
| Start date | Jun 1, 2001 |
| Completion | May 10, 2007 |
| First posted | Jun 11, 2001 |
| Last update posted | Jul 2, 2017 |
| 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: