Ignite Creation Date:
2024-05-06 @ 8:24 PM
Last Modification Date:
2024-10-26 @ 3:26 PM
Study NCT ID:
NCT06365749
Status:
NOT_YET_RECRUITING
Last Update Posted:
2024-04-15
First Post:
2023-11-21
Brief Title:
Genetic Feature of Congenital Hearing Loss in Chinese Population
Sponsor:
Dan Bing
Organization:
Tongji Hospital
Study Overview
Official Title:
Exome Sequencing Explored the Genetic Characteristics Congenital Hearing Loss in Chinese Population
Status:
NOT_YET_RECRUITING
Status Verified Date:
2024-04
Last Known Status:
None
Delayed Posting:
No
If Stopped, Why?:
Not Stopped
Has Expanded Access:
False
If Expanded Access, NCT#:
N/A
Has Expanded Access, NCT# Status:
N/A
Acronym:
None
Brief Summary:
Congenital hearing loss as well as hearing loss present at birth is one of the most common chronic conditions in children with a prevalence of permanent bilateral hearing loss of 283 per 1000 children of primary school age which is mainly caused by genetic factors The goal of this observational study is to learn about novel causative genes in infants with hearing loss in the Chinese population The main problem it aims to deal with are
to present the genetic characteristics of the infant with hearing loss in the Chinese population
to build up a prognostic model base on diverse data
Participants will be asked to receive audiological tests and collection of the peripheral blood sample
to present the genetic characteristics of the infant with hearing loss in the Chinese population
to build up a prognostic model base on diverse data
Participants will be asked to receive audiological tests and collection of the peripheral blood sample
Detailed Description:
None
Study Oversight
Has Oversight DMC:
None
Is a FDA Regulated Drug?:
False
Is a FDA Regulated Device?:
False
Is an Unapproved Device?:
None
Is a PPSD?:
None
Is a US Export?:
None
Is an FDA AA801 Violation?:
None