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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05866770
Other study ID # AI5837
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date September 11, 2023
Est. completion date June 30, 2026

Study information

Verified date October 2023
Source Cochlear
Contact Komal Arora
Phone +61 432 218 588
Email karora@cochlear.com
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

A feasibility, prospective, multi-centre, repeated measures investigation evaluating the application of hearing aid technologies to signal processing for adult cochlear implant recipients


Description:

The Research System is comprised of several components: the processing unit, fitting software and accessories. The sound processor converts sounds into electrical signals, which it sends, via a coil, to an implant to provide hearing sensation. The application of hearing aid technologies to Cochlear Implant recipients may provide benefit through matching the signal processing technologies across ears for bimodal listeners, enhance performance for CI-alone listening, and potentially lead to efficiency in algorithm development.


Recruitment information / eligibility

Status Recruiting
Enrollment 150
Est. completion date June 30, 2026
Est. primary completion date June 30, 2026
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Eighteen years of age or older - User of CI600, CI500 or CI24RE implant - At least 3 months experience with a TGA approved Nucleus cochlear implant in at least one ear - Fluent speaker of English - A word speech recognition score of 20% or more when using the cochlear implant alone* - Willing and able to provide written informed consent *This can be based on clinical data if collected within the last 12 months Exclusion criteria: - Unable or unwilling to comply with the requirements of the clinical investigation as determined by the Investigator. - 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. - Current participation, or participation in another interventional clinical study/trial in the past 30 days, involving an investigational drug or device. (Unless the other investigation was/is a Cochlear sponsored investigation and determined by the investigator or Sponsor to not impact this investigation.

Study Design


Related Conditions & MeSH terms


Intervention

Device:
U8
The U8 Research System
N8 sound processor
Nucleus 8 sound processor

Locations

Country Name City State
Australia HEARnet Clinical Studies Carlton Victoria
Australia Cochlear Melbourne Melbourne E. Melbourne
Australia Cochlear Macquarie Sydney New South Wales

Sponsors (2)

Lead Sponsor Collaborator
Cochlear Avania

Country where clinical trial is conducted

Australia, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent correct monosyllabic word scores. To determine whether the research system provides non-inferior performance to the Nucleus 8 sound processor for monosyllabic words in quiet CNC words at 60 dB SPL (sound pressure level)
Word recognition is a score of the number of words correctly repeated, expressed as a percentage. Higher percentage scores indicate a better outcome.
3 months
Primary Adaptive sentence in noise scores (AuSTIN) To determine whether the research system provides non-inferior performance to the Nucleus 8 sound processor for sentences in noise. 3 months
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