Clinical trial
A Genetic Analysis of Usher Syndrome in Ashkenazi Jews
NCT00016471 · National Center for Research Resources (NCRR), NIH · Completed
Key facts
| NCT number | NCT00016471 |
|---|---|
| Title | A Genetic Analysis of Usher Syndrome in Ashkenazi Jews |
| Official title | A Genetic Analysis of Usher Syndrome in Ashkenazi Jews |
| Lead sponsor | National Center for Research Resources (NCRR), NIH |
| Status | Completed |
| Study type | Observational |
| Conditions | Usher Syndrome, Retinitis Pigmentosa, Congenital Hearing Impairment |
| Intervention type | Procedure |
| Interventions | Audiogram, Electroretinogram |
| Start date | Mar 1, 2001 |
| Completion | Feb 1, 2002 |
| First posted | May 9, 2001 |
| Last update posted | Jun 24, 2005 |
| 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: