Clinical trial
Genetic Analysis of Human Hereditary Hearing Impairment
NCT00001606 · National Institute on Deafness and Other Communication Disorders (NIDCD), NIH · Terminated
Key facts
| NCT number | NCT00001606 |
|---|---|
| Title | Genetic Analysis of Human Hereditary Hearing Impairment |
| Official title | Genetic Analysis of Human Hereditary Hearing Impairment |
| Lead sponsor | National Institute on Deafness and Other Communication Disorders (NIDCD), NIH |
| Status | Terminated |
| Study type | Observational |
| Conditions | Partial Hearing Loss |
| Enrollment | 404 |
| Start date | Sep 8, 1997 |
| Completion | Apr 7, 2015 |
| First posted | Nov 4, 1999 |
| Last update posted | Dec 17, 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: