LeállítvaFázis nélkül
Cross-sectional and Prospective Study to Characterize Early-onset Presbycusis
Megadott ok: Sponsor decision
A legfontosabb adatok
- Hol
- Tampa (Egyesült Államok)A helyszín megnézése
Helyszínek itt: Egyesült Államok
- The University of South Florida Board of TrusteesTampa, Egyesült ÁllamokNo longer taking part
A vizsgálat adatai
- Ki végzi
- Sensorion
- Azonosító
- NCT06354010
- A regiszteradat frissítve
- 2026. október 26.
- Eredeti leírás
The purpose of this study is to characterize and assess the evolution of hearing impairment of patients with adulthood-onset bilateral sensorineural hearing loss carrying mutations on GJB2 gene.A teljes eredeti leírásKevesebb
The purpose of this study is to characterize and assess the evolution of hearing impairment of patients with adulthood-onset bilateral sensorineural hearing loss carrying mutations on GJB2 gene.
Bevonási feltételek: Female or Male patients ≥30 and ≤55 years old; Bilateral hearing loss first noticed after the age of 16 years old; Documented genotyping results showing mutations in GJB2 gene.
Kizáró feltételek: Deafness with a known, non-genetic cause; To the opinion of the investigator, unable and/or unwilling to comply with all the protocol requirements and/or study procedures.