Actively Recruiting

Phase Not Applicable
Age: 18Years +
All Genders
ID06723262

Contribution to Speech Perception of a Tonotopy-based Fitting for Patients With Cochlear Implants for 6 Months With a Conventional Setting: Prospective Cross-sectional Study

Led by MED-EL Elektromedizinische Geräte GesmbH · Updated on 2026-05-06

25

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are investigating speech recognition in noise using two different cochlear implant fitting methods: tonotopic fitting (FS4T) and conventional non-tonotopic fitting (FS4noT). The study focuses on adults who have used a MED-EL cochlear implant with the FS4noT strategy for 6 months. This research aims to understand if tonotopic fitting, which adjusts frequencies based on individual cochlear anatomy, improves speech perception compared to the standard fitting. Participants will experience a tonotopic fitting (FS4T) setting for 6 weeks after being implanted for 6 months with the conventional FS4noT setting. The FS4T fitting uses CT scan data and 3D reconstruction to tailor the cochlear implant frequencies to the patient’s specific cochlear structure. The study compares speech recognition in noise and quiet, as well as subjective auditory spatial perception, between the two fitting methods. During the study, participants’ speech recognition abilities in noise and quiet will be assessed 6 weeks after starting FS4T fitting. Subjective auditory spatial perception will be evaluated at the beginning of FS4T fitting and again after 6 weeks. The study is prospective, open, and cross-sectional, with all evaluations focusing on the effects of the tonotopic fitting compared to the conventional one. Participants will be monitored for changes in hearing performance during the 6-week FS4T period.

CONDITIONS

Brief Title

Speech Perception of a Tonotopy-based Fitting for Cochlear Implant Recipients for 6 Months With Conventional Setting

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patient (18 years or older) speaking French
  • Patient who fulfils the criteria for cochlear implantation
Not Eligible

You will not qualify if you...

  • Retro-cochlear pathology such as auditory neuropathy or vestibular schwannoma

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive a tonotopic cochlear implant fitting (FS4T) and use this setting for 6 weeks to compare speech recognition and auditory perception with their conventional cochlear implant setting.

1 visit at start of fitting and assessments 6 weeks later

Trial Site Locations

Total: 1 location

1

CHU

Limoges, France, 87000

Actively Recruiting

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Research Team

V

Vincent Péan, PhD

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

OTHER

Number of Arms

1

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