Viewing Study NCT05898659



Ignite Creation Date: 2024-05-06 @ 7:07 PM
Last Modification Date: 2024-10-26 @ 3:00 PM
Study NCT ID: NCT05898659
Status: RECRUITING
Last Update Posted: 2023-11-01
First Post: 2023-06-02

Brief Title: Comparison in New Cochlear Implanted Subjects of a Tonotopy-based Bimodal Fitting With or Without Synchronization
Sponsor: MED-EL Elektromedizinische Geräte GesmbH
Organization: MED-EL Elektromedizinische Geräte GesmbH

Study Overview

Official Title: Comparison of a Bimodal Fitting With Synchronization and a Conventional Bimodal Fitting in Newly Implanted Cochlear Patient Prospective Monocentric Randomized Double-blind Crossover Study
Status: RECRUITING
Status Verified Date: 2023-10
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: Main objective

For a bimodal fitting hearing aid HA cochlear implant CI Comparison of a tonotopy based fitting strategy with synchronization between HA and CI ABFS to a tonotopy based fitting strategy without synchronization ABFnoS for the accuracy of sound localization

Secondary objectives

Comparison of ABFS to ABFnoS for the bias of sound localization Comparison of ABFS to ABFnoS for speech perception in noise Comparison of ABFS to ABFnoS for the auditory skills experienced by the subject
Detailed Description: Introduction Cochlear implantation allows the rehabilitation of profound bilateral deafness restoring speech perception and verbal communication when the traditional hearing aid no longer provides satisfactory hearing gain

A cochlear implant includes an electrode array and its functioning is based on the principle of cochlear tonotopy Each electrode encodes a frequency spectrum according to its position in the cochlea high frequencies are assigned to the basal electrodes and low frequencies to the apical electrodes The cochlear implant thus breaks down the frequency spectrum into a number of frequency bands via bandpass filters corresponding to the number of electrodes in the implant During the fitting these bands can be modified by the audiologist

MED-EL has developed a fitting strategy ABF that allows from a post-operative scanner to calculate the theoretical characteristic frequency of neurons stimulated by each electrode contact and to transmit this information to the fitting software of the CI

Bimodal hearing refers to the use of a CI in one ear with a HA on the contralateral side

This association allows for adults and children a better perception of speech in quiet and in noise a better perception of music hearing comfort better sound quality better localization of sound and consequently a better quality of life compared to unilateral CI alone However there is great variability in the integration process while some bimodal users show substantial benefits others receive little or no benefit

This variability could be due to different processing times between CI and contralateral HA

Recently MED-EL Austria has developed a new approach to synchronize the treatment time of the CI with that of the contralateral HA via the fitting software This new approach takes into account the different treatment times between CI and contralateral HA and allows synchronization between the 2 systems CI and HA

This strategy ABFS could therefore allow a better integration of information in bimodal hearing and in particular improve the sound localization compare to a strategy without synchronization ABFnoS

Main objective

For a bimodal fitting hearing aid HA cochlear implant CI Comparison of a tonotopy based fitting strategy with synchronization between HA and CI ABFS to a tonotopy based fitting strategy without synchronization ABFnoS for the accuracy of sound localization

Secondary objectives

Comparison of ABFS to ABFnoS for the bias of sound localization Comparison of ABFS to ABFnoS for speech perception in noise Comparison of ABFS to ABFnoS for the auditory skills experienced by the subject

Plan of the study

It is a prospective open monocentric randomized crossover study Measures will be done on the patient at 6 weeks and 12 weeks post-activation

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