N/A
N=20
Innovations in Clinical Care of CE Approved Nucleus Cochlear Implant Recipients
Hearing Loss
Bottom Line
View on ClinicalTrials.gov: NCT05270876 ↗Enrolled (actual)
20
Serious AEs
0.0%
Results posted
Dec 2024
Primary outcome: Primary: Mean Difference Between Standard and Novel Fitting Method for Monosyllabic Word Scores in Quiet — 3.8 difference in percentage correct answers
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- Cochlear Implant and sound processor device fitting paradigm or diagnostic/measurement technique (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Cochlear
- Primary completion
- Mar 2023
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Mean Difference Between Standard and Novel Fitting Method for Monosyllabic Word Scores in Quiet |
3.8 | — |
Summary
This study is to evaluate new approaches to device fitting and diagnostics for cochlear implant users. The evaluation can be performed in the laboratory in an acute session or in real world environments with take-home device use to further validate their benefits. Each feature will be tested in a sub-study specific to that hearing care model. On average, each sub-study is expected to include approximately 20 subjects.
Eligibility Criteria
Inclusion Criteria
- Users of a CE approved Nucleus cochlear implant, resulting in open set speech understanding
- At least three months of experience with the cochlear implant.
- Older than 18 years when entering the study.
- Subject is fluent speaker in the language used for assessments.
- Open set speech understanding sufficient to complete the study protocol as judged by the investigator.
- Willing and able to provide written informed consent
Exclusion Criteria
- Unable or unwilling to comply with the requirements of the clinical investigation as determined by the investigator.
- Additional health factors, known to the investigator, that would prevent or restrict participation in the audiological evaluations.
- Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling.
- Cochlear employees or employees of Contract Research Organizations or contractors engaged by Cochlear for the purposes of this investigation.
- Currently participating, or participated within the last 30 days, in another interventional clinical investigation/trial involving an investigational drug or device.
Data sourced from ClinicalTrials.gov (NCT05270876). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.