Study of Sound and Speech Perception in New Cochlear Implanted Subjects Using or Not an Anatomy-based Fitting

Sponsor
MED-EL Elektromedizinische Geräte GesmbH (Industry)
Overall Status
Recruiting
CT.gov ID
NCT05230498
Collaborator
(none)
24
1
2
17.9
1.3

Study Details

Study Description

Brief Summary

Main objective:

Compare the recognition of environmental sounds with an anatomy-based fitting and with a default fitting adult patients newly implanted with a MED-EL cochlear implant.

Secondary objectives:

Compare speech recognition in quiet with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant.

Compare speech recognition in noise with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant.

Condition or Disease Intervention/Treatment Phase
  • Device: anatomy-based fitting then default fitting
  • Device: default fitting then anatomy-based fitting
N/A

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. The fitting software developed by the manufacturers proposed a default fitting with a lower limit between 100 and 250 Hz according to the brands and an upper limit of about 8500 Hz. The frequency bands assigned to each electrode follow a logarithmic scale with the high frequencies for the basal electrodes and the low frequencies for the apical electrodes. This distribution takes into account the number of active electrodes but does not take into account the anatomy and the natural cochlear tonotopy specific to each patient. Several studies have analyzed the anatomical variations of the cochlear dimensions: size of the cochlea and the ratio between the contact surfaces of the electrodes with the cochlea are variable from one patient to another. The insertion depth during surgery is also variable due to parameters related to the patients as well as to the operator, which seems to impact the understanding of speech in noise. Mathematical algorithms have recently been developed to estimate the cochlear tonotopy of each patient from a CT scan assessment. CT imaging of the implanted ear combined with 3D reconstruction software, provides cochlear length measurements Using this approach it is possible to measure the position of each electrode relative to the cochlear apex. Recently, MED-EL (Austria) has developed a new approach based on CT-scan and tuning of the frequencies associated with each electrode using anatomical information of position of the electrodes in the cochlea: this fitting is called anatomy-based fitting.

Main objective:

Compare the recognition of environmental sounds with an anatomy-based fitting and with a default fitting adult patients newly implanted with a MED-EL cochlear implant.

Secondary objectives:

Compare speech recognition in quiet with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant.

Compare speech recognition in noise with an anatomy-based fitting and with a default fitting in adult patients newly implanted with a MED-EL cochlear implant.

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 Design

Study Type:
Interventional
Anticipated Enrollment :
24 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Two arms A and B: Arm A: patient's fitting with default fitting --> 6 weeks use --> tests and patient's fitting with anatomy-based fitting --> 6 weeks use --> tests Arm B: patient's fitting with anatomy-based fitting --> 6 weeks use --> tests and patient's fitting with default fitting --> 6 weeks use --> testsTwo arms A and B:Arm A: patient's fitting with default fitting --> 6 weeks use --> tests and patient's fitting with anatomy-based fitting --> 6 weeks use --> tests Arm B: patient's fitting with anatomy-based fitting --> 6 weeks use --> tests and patient's fitting with default fitting --> 6 weeks use --> tests
Masking:
Double (Participant, Investigator)
Masking Description:
Double blind study: the patient and the investigator don't know the fitting.
Primary Purpose:
Other
Official Title:
Comparison of an Anatomy-based Fitting and a Conventional Fitting in Newly Implanted Cochlear Patients. Prospective Monocentric Randomized Double-blind Crossover Study.
Actual Study Start Date :
Feb 15, 2022
Anticipated Primary Completion Date :
Aug 15, 2023
Anticipated Study Completion Date :
Aug 15, 2023

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Cochlear Implant (CI) with default fitting then anatomy-based fitting

Cochlear Implant with default fitting first during 6 weeks then with anatomy-based fitting during 6 weeks

Device: default fitting then anatomy-based fitting
Cochlear implant with anatomy-based fitting then default fitting

Active Comparator: Cochlear Implant (CI) with anatomy-based fitting then default fitting

Cochlear Implant with anatomy-based fitting during 6 weeks then with default fitting during 6 weeks

Device: anatomy-based fitting then default fitting
Cochlear implant with anatomy-based fitting then default fitting

Outcome Measures

Primary Outcome Measures

  1. Recognition of Environmental sounds [at 6 weeks post-activation]

    The environmental sound recognition is evaluated with the Environmental Sound Identification Test (TISE, Treville-Protain et al. 2019). The patient has to recognize 24 environmental sounds. Each good answer is scored 1 yielding a total between 0 and 1 (or 0% and 100%).

  2. Recognition of Environmental sounds [at 12 weeks post-activation]

    The environmental sound recognition is evaluated with the Environmental Sound Identification Test (TISE, Treville-Protain et al. 2019). The patient has to recognize 24 environmental sounds. Each good answer is scored 1 yielding a total between 0 and 1 (or 0% and 100%).

Secondary Outcome Measures

  1. Speech recognition in quiet [at 6 weeks post-activation]

    The speech recognition in quiet is evaluated with 3 lists of 10 disyllabic words. The patient has to recognize 30 words. Each good answer is scored 1 yielding a total between 0 and 1 (or 0% and 100%).

  2. Speech recognition in quiet [at 12 weeks post-activation]

    The speech recognition in quiet is evaluated with 3 lists of 10 disyllabic words. The patient has to recognize 30 words. Each good answer is scored 1 yielding a total between 0 and 1 (or 0% and 100%).

  3. Speech recognition in noise [at 6 weeks post-activation]

    The speech recognition in noise is evaluated with the French-language "Rapid speech in noise" (VRB) test (Leclerc et al. 2018). The speech level is at 65 dB SPL. The patient has to recognize 3 target words by sentence. The 8 sentences are played with signal-to-noise ratios between +18 dB and -3 dB by steps of 3 dB. The SRT50 (threshold for 50% intelligibility in noise) is obtained by SRT50 = 19,5 - R, with R = number of correct answers (on 24).

  4. Speech recognition in noise [at 12 weeks post-activation]

    The speech recognition in noise is evaluated with the French-language VRB test (Leclerc et al. 2018). The speech level is at 65 dB SPL. The patient has to recognize 3 target words by sentence. The 8 sentences are played with signal-to-noise ratios between +18 dB and -3 dB by steps of 3 dB. The SRT50 (threshold for 50% intelligibility in noise) is obtained by SRT50 = 19,5 - R, with R=number of correct answers (on 24).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Adult patient (>= 18 years old) speaking French

  • Patient who fulfils the criteria for cochlear implantation

Exclusion Criteria:
  • retro-cochlear pathology: auditory neuropathy, vestibular schwannoma

Contacts and Locations

Locations

Site City State Country Postal Code
1 CHU Bordeaux France 33076

Sponsors and Collaborators

  • MED-EL Elektromedizinische Geräte GesmbH

Investigators

  • Principal Investigator: Damien Bonnard, Dr, University Hospital, Bordeaux

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
MED-EL Elektromedizinische Geräte GesmbH
ClinicalTrials.gov Identifier:
NCT05230498
Other Study ID Numbers:
  • MEDEL_anatfit_Bordeaux_study
First Posted:
Feb 9, 2022
Last Update Posted:
Apr 6, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by MED-EL Elektromedizinische Geräte GesmbH
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 6, 2022