Clinical trial
Natural History and Genetic Studies of Usher Syndrome
NCT00106743 · National Eye Institute (NEI), NIH · Completed
Key facts
| NCT number | NCT00106743 |
|---|---|
| Title | Natural History and Genetic Studies of Usher Syndrome |
| Official title | Natural History and Genetic Studies of Usher Syndrome |
| Lead sponsor | National Eye Institute (NEI), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Retinitis Pigmentosa Syndromic, Congenital Deafness, Usher Syndrome, Retinitis Pigmentosa and Deafness, Retinitis Pigmentosa |
| Enrollment | 249 |
| Start date | Mar 21, 2005 |
| Completion | Apr 30, 2019 |
| First posted | Mar 30, 2005 |
| Last update posted | Dec 12, 2019 |
| 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: