Congenital deafness
Information
- Disease name
- Congenital deafness
- Disease ID
- Description
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00106743 | Completed | Natural History and Genetic Studies of Usher Syndrome | March 21, 2005 | April 30, 2019 | |
| NCT00400413 | Completed | N/A | Neuroanatomy of Reading in Congenital Deafness. | November 2003 | August 2011 |
| NCT03319524 | Completed | Clinical and Genetic Testing of Patients With Usher Syndrome | May 17, 2017 | June 1, 2018 | |
| NCT06370351 | Not yet recruiting | Phase 1/Phase 2 | A Phase I/II Clinical Trial With SENS-501 in Children Suffering From Severe to Profound Hearing Loss Due to Otoferlin (OTOF) Mutations | April 30, 2024 | April 2031 |
| NCT06365749 | Not yet recruiting | Genetic Feature of Congenital Hearing Loss in Chinese Population | April 23, 2024 | November 23, 2026 | |
| NCT05402813 | Recruiting | Natural History in Children up to 10 Years With Moderate to Profound Hearing Loss Due to Mutations in GJB2 / OTOF Genes | November 18, 2022 | November 18, 2026 | |
| NCT03866850 | Terminated | Degenerative Consequences of Congenital Deafness | August 1, 2019 | April 4, 2023 | |
| NCT04350619 | Unknown status | NGS Assessment of Congenitally Deafned Children and Neonatal Deafness Screnning | April 30, 2020 | April 2021 |