Sensorineural Hearing Loss Clinical Trial
— ABFmultiOfficial title:
Anatomy-Based Fitting in Unexperienced Cochlear Implant Users
Severe to profound hearing loss affects 0,8% of the global population. For these people, a conventional hearing aid often does not provide sufficient benefit. However, these people can benefit from a cochlear implant (CI). A CI needs to be individually programmed (fitted) for each recipient. A fitting "map" is defined as a set of electrical parameters that are individually adapted to a recipient's needs to achieve optimal sound perception. At present, most CI recipients are fitted with a default frequency allocation map that doesn't take individual variability in size and shape of the cochlea into account. In this study, a fitting strategy based on the post-operative CT scan, that will allow the audiologist to set a frequency-band distribution for CI fitting that may be more closely aligned to the natural tonotopic frequency distribution of a normal hearing cochlea, will be evaluated.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | January 2025 |
Est. primary completion date | January 2025 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - Age = 18 years - Post-lingual onset of severe to profound sensory-neural hearing loss in the implanted ear(s) - Post-operative Computed Tomography (CT) scan of the CI electrode available - Pre-operative result of pure-tone audiometry, speech test in quiet and in noise available - Subject implanted with MED-EL cochlear implant(s) - Subjects received a Flex28, FlexSoft or Standard electrode - Subject planned to receive a SONNET 2 or RONDO 3 audio processor on the newly implanted side - Audio processor not yet activated on the newly implanted side - The most apical active electrode contact has to be inserted at least 450° - Minimum of 10 active channels can be activated - Fluent in the language of the test centre - Signed and dated Informed Consent Form (ICF) before the start of any study-specific procedure Exclusion Criteria: - Lack of compliance with any inclusion criteria - Electric Acoustic Stimulation (EAS) user (user of an EAS audio processor) - Implanted with C40+, C40X and C40C - Implanted with an Auditory Brainstem Implant (ABI) or Split electrode array - Anything that, in the opinion of the Investigator, would place the subject at increased risk or pre-clude the subject's full compliance with or completion of the study |
Country | Name | City | State |
---|---|---|---|
Belgium | UZ Brussel | Brussel |
Lead Sponsor | Collaborator |
---|---|
Universitair Ziekenhuis Brussel |
Belgium,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Speech recognition test in quiet (S0): percentage correctly identified phonemes | 3 months post-activation | ||
Primary | Speech recognition test in quiet (S0): percentage correctly identified phonemes | 6 months post-activation | ||
Secondary | Speech recognition test in noise (S0N0): the speech reception threshold in dB SNR | 3 months post-activation | ||
Secondary | Speech recognition test in noise (S0N0): the speech reception threshold in dB SNR | 6 months post-activation | ||
Secondary | Result of the pitch matching test: frequency difference in semitones | 3 months post-activation | ||
Secondary | Result of the pitch matching test: frequency differences in semitones | 6 months post-activation | ||
Secondary | Result of the perception of timbre test: Score on Visual Analog Scale (VAS) | Patients have to rate the timbre on a visual analog scale (VAS) ranging from 0 to 10, where a higher score reflects a better outcome. | 3 months post-activation | |
Secondary | Result of the perception of timbre test: Score on Visual Analog Scale (VAS) | Patients have to rate the timbre on a visual analog scale (VAS) ranging from 0 to 10, where a higher score reflects a better outcome. | 6 months post-activation | |
Secondary | Result of the consonance and dissonance rating test: Plot of pleasantness over frequency interval and modulation measure | 3 months post-activation | ||
Secondary | Result of the consonance and dissonance rating test: Plot of pleasantness over frequency interval and modulation measure | 6 months post-activation | ||
Secondary | Result of the speech contrast discrimination test: Psychometric function of phoneme categorization | 3 months post-activation | ||
Secondary | Result of the speech contrast discrimination test: Psychometric function of phoneme categorization | 6 months post-activation | ||
Secondary | Patient reported outcome- Hearing Implant Sound Quality Index (HISQUI): Total score and classification of self-perceived auditory benefit | 1 day visit (At the activation of the sound processor) | ||
Secondary | Patient reported outcome- Hearing Implant Sound Quality Index (HISQUI): Total score and classification of self-perceived auditory benefit | 3 months post-activation | ||
Secondary | Patient reported outcome- Hearing Implant Sound Quality Index (HISQUI): Total score and classification of self-perceived auditory benefit | 6 months post-activation | ||
Secondary | Datalogging data: Average numbers of hours per day | 2 weeks post-activation | ||
Secondary | Datalogging data: Average numbers of hours per day | 1 months post-activation | ||
Secondary | Datalogging data: Average numbers of hours per day | 3 months post-activation | ||
Secondary | Datalogging data: Average numbers of hours per day | 6 months post-activation |
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