Hearing Impairment, Sensorineural Clinical Trial
Official title:
A Pre-Marketing, Prospective, Single-Site, Open-Label, Within-Subject, Pilot, Interventional Study of Adult Cochlear Implant Speech Perception With the CP1150 Sound Processor Compared With the Next Generation of Signal Processing Technology
NCT number | NCT05286385 |
Other study ID # | CLTD5818 |
Secondary ID | |
Status | Completed |
Phase | N/A |
First received | |
Last updated | |
Start date | May 30, 2022 |
Est. completion date | June 29, 2022 |
Verified date | July 2022 |
Source | Cochlear |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
This clinical study aims to investigate speech performance in quiet with an OTE Sound Processor with modified firmware compared with the commercially available CP1150. The study also investigates CP1110 and CP1150 with Forward Focus.
Status | Completed |
Enrollment | 10 |
Est. completion date | June 29, 2022 |
Est. primary completion date | June 29, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: 1. Aged 18 years or older 2. Post lingually deafened 3. Implanted with the CI600 Series, CI500 Series or Freedom Series 4. At least 6 months experience with a cochlear implant. 5. At least 3 months experience with a CP910/920, CP950, CP1150, or CP1000 Sound Processor 6. MAP Total Stimulation Rate of 7.2kHz or greater 7. Able to score 30% or more with CI alone on a monosyllabic words in quiet test 8. Willingness to participate in and to comply with all requirements of the protocol 9. Fluent speaker in English as determined by the investigator 10. Willing and able to provide written informed consent Exclusion Criteria: 1. Additional disabilities that would prevent participation in evaluations. 2. Implant location that would result in undesirable hearing performance or discomfort with an off-the-ear sound processor, as determined by the investigator. 3. Unable or unwilling to comply with the requirements of the clinical investigation, as determined by the Investigator. 4. Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child, or sibling. 5. Cochlear employees or employees of Contract Research Organisations or contractors engaged by Cochlear for the purposes of this investigation. 6. Currently participating or participated in another interventional clinical study/trial in the past 30 days unless (if less than 30 days) the prior investigation was Cochlear sponsored and determined by the investigator to not impact clinical findings of this investigation. 7. Implanted with other active implantable medical devices (e.g. pacemaker, defibrillator). |
Country | Name | City | State |
---|---|---|---|
Australia | Cochlear Sydney | Macquarie Park | New South Wales |
Lead Sponsor | Collaborator |
---|---|
Cochlear | Avania |
Australia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Speech perception in quiet using an OTE Sound Processor | Paired difference in percentage CNC Words correct in quiet with the CP1150 Sound Processor and CP1150 Sound Processor with modified firmware. | One day | |
Secondary | Speech perception in quiet using an OTE Sound Processor using FF combined with standard microphone directionality | Paired difference in percentage CNC Words correct in quiet with the CP1150 Sound Processor and CP1150 Sound Processor with FF | One day | |
Secondary | Speech perception in quiet with CP1150 and CP1110 Sound Processors | Paired difference in percentage CNC Words correct in quiet with the CP1150 Sound Processor and CP1110 Sound Processor | One day |
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