Clinical trial
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan
NCT00341874 · National Institute on Deafness and Other Communication Disorders (NIDCD), NIH · Enrolling by invitation
Key facts
| NCT number | NCT00341874 |
|---|---|
| Title | Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan |
| Official title | Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan |
| Lead sponsor | National Institute on Deafness and Other Communication Disorders (NIDCD), NIH |
| Status | Enrolling by invitation |
| Study type | Observational |
| Conditions | Hearing Disorder |
| Enrollment | 24,000 |
| Start date | Mar 16, 2000 |
| First posted | Jun 21, 2006 |
| Last update posted | Jan 16, 2026 |
| Countries | Pakistan |
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: