Viewing Study NCT05946057



Ignite Creation Date: 2024-05-06 @ 7:15 PM
Last Modification Date: 2024-10-26 @ 3:03 PM
Study NCT ID: NCT05946057
Status: RECRUITING
Last Update Posted: 2024-06-25
First Post: 2023-06-05

Brief Title: Otoferlin Patient Registry and Natural History Study
Sponsor: Tobias Moser
Organization: University Medical Center Goettingen

Study Overview

Official Title: Patient Registry for Individuals With Otoferlin-Associated Hearing Loss
Status: RECRUITING
Status Verified Date: 2024-09
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: This registry is designed to collect comprehensive information about the molecular genetic diagnoses of individuals with otoferlin-associated hearing impairment and clinical information to support a natural history study
Detailed Description: A patient registry in both German and English languages has been established for patients with hereditary hearing impairment due to variants in otoferlin OTOF The study is conducted in accordance with the current version of the Declaration of Helsinki The study protocol and database structure have been approved by the Ethics Committee of the University Medical Center Göttingen

Main objective criterion

To increase understanding of natural history types of genetic variants and to facilitate clinical and basic research on otoferlin-associated hearing impairment

Secondary objective criterion

To improve knowledge to better characterize individuals with otoferlin-associated hearing impairment in the long term and create prerequisites for improved patient tailored therapy and care

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