Viewing Study NCT06507007



Ignite Creation Date: 2024-10-26 @ 3:35 PM
Last Modification Date: 2024-10-26 @ 3:35 PM
Study NCT ID: NCT06507007
Status: NOT_YET_RECRUITING
Last Update Posted: None
First Post: 2024-06-24

Brief Title: Genetic and Epigenetic Background of Inner Ear Dysfunction in Turner Syndrome
Sponsor: None
Organization: None

Study Overview

Official Title: Genetic and Epigenetic Background of Inner Ear Dysfunction in Turner Syndrome
Status: NOT_YET_RECRUITING
Status Verified Date: 2024-07
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of this case-control study is to pave the way for new revolutionary treatment measures within hearing loss that could either replace or delay the need for hearing aids The study focuses on people with Turner syndrome TS

The aim is to find out if there are specific DNA methylation patterns andor RNA expression profiles linked to sensorineural hearing loss SNHL in people with TS Additionally the structure and function of the inner ear in these individuals will be examined to see if there is a connection to their epigenetic profile

The main question it aims to answer is Does epigenetics constitute a common denominator for some of the unexplained SNHL cases

Turner Syndrome TS represents an ideal model for studying epigenetics related to sensorineural hearing loss SNHL

Participants will undergo the following tests

Ear examinations
Hearing tests
Balance tests
Blood tests
MRI scans
CBCT cone-beam computed tomography scans
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None