PAS-SSD: Investigation to Evaluate the Safety and Effectiveness of Cochlear Implantation in Children and Adults With Unilateral Hearing Loss/Single-sided Deafness
Study Details
Study Description
Brief Summary
The aim of the study is to assess the continued efficacy and safety of cochlear implantation in participants aged 5 years and above with Unilateral Hearing Loss (UHL)/Single Sided Deafness (SSD) supporting a change indication for use.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
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N/A |
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Other: Children and adults with unilateral hearing loss/single-sided deafness
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Device: The Cochlear™ Nucleus® Cochlear Implant (CI) System
The Cochlear™ Nucleus® CI systems are designed to provide useful hearing. The system works by converting sound in the environment into electric pulses that stimulate the auditory nerve, allowing the brain to perceive sound. The Cochlear™ Nucleus® CI system has implanted and external components.
Implanted component:
The CI is surgically implanted under the skin behind the ear. It includes a receiver/stimulator to receive and decode the electrical signals from the sound processor and an electrode to deliver these signals to the cochlear.
External components:
The external components include a sound processor, and associated accessories and cables. The system is programmed by a Cochlear proprietary programming system, Custom Sound®.
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Outcome Measures
Primary Outcome Measures
- Change in sentence in noise scores at 12 months post-activation in the binaural (CI and normal hearing (NH)) listening condition compared to preoperatively in the best listening (NH alone or NH and hearing aid) condition in 3 speaker configurations. [pre-implantation, 12 months post-activation]
Measured with the Bamford-Kowal-Bench Sentence in Noise test (BKB-SIN). List of sentences are presented at 65 dBA with the level of noise varied stepwise at fixed signal to noise ratio to obtain a Speech Reception Threshold (SRT) where participants are able to repeat key words 50% of the time. Score range is not specified as metric is adaptive; lower scores indicate better performance. The 3 speaker configurations are: speech front/noise front; speech front/noise to NH ear; speech front/noise to poorer ear.
- Number of procedure and device related adverse events classified by type, frequency and severity. [36 months post-activation]
Secondary Outcome Measures
- Change in participant reported spatial hearing at 12 months post-activation compared to pre-operative ratings. [pre-implantation, 12 months post-activation]
Assessed via Speech, Spatial, and Qualities of Hearing Scale (SSQ) questionnaire (parent or participant version dependent on age). Rating ranges from 0 (no ability) to 10 (complete ability). Higher scores indicate greater perceived abilities.
- Change in word recognition at 12 months post-activation in the CI alone condition compared to preoperative aided condition in the poorer hearing ear alone. [pre-implantation, 12 months post-activation]
Measured via the Consonant-Nucleus-Consonant (CNC) Word Recognition Test. The score is the total number of words correct expressed as percent correct (range of 0-100); higher score is better.
Eligibility Criteria
Criteria
Inclusion Criteria:
• Individuals 18 years or older (Group A)
Ear to be Implanted:
Severe sensorineural hearing loss (HL) defined as: Pure-tone average at 0.5, 1, 2, 4 kHz
80 dB HL ; Aided Consonant-Nucleus-Consonant Test (CNC) score ≤5% and
Normal Hearing Ear:
Normal or near normal hearing defined as an average of (0.5, 1, 2, 4kHz) ≤ 30 dB HL
• Children 5 years to 17 years, 11 months (Group B)
Ear to be Implanted:
Severe sensorineural HL defined as: Pure-tone average at 0.5, 1, 2, 4 kHz >80 dB HL; Aided CNC score ≤5% and
Normal Hearing Ear:
Normal or near normal hearing defined as an average of (0.5, 1, 2, 4kHz) ≤ 30 dB HL
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Previous experience with a current conventional treatment option for unilateral [SSD] HL (HA, bone-conduction device, or CROS technology), if no previous experience a minimum trial period of two weeks is required
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English spoken as a primary language
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Willing and able to provide written informed consent
Exclusion Criteria:
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Ossification, abnormal cochlear nerve or any other cochlear anomaly that might prevent complete insertion of the electrode array
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Previous cochlear implantation
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Hearing loss of neural or central origin, including auditory neuropathy
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Duration of profound sensorineural HL >10 years per self-report
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Active / chronic middle-ear infection; conductive HL in either ear
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Medical or psychological conditions that contraindicate undergoing surgery as determined by the Investigator
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Unrealistic expectations on the part of the participant/family, regarding the possible benefits, risks, and limitations that are inherent as determined by the Investigator
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Evidence of and/or suspected cognitive or developmental concern
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Unable or unwilling to comply with the requirements of the clinical investigation as determined by the Investigator
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Investigator site personnel directly affiliated with this study and/or their immediate families; immediate family is defined as a spouse, parent, child or sibling
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Cochlear employees or employees of Contract Research Organizations (CROs) or contractors engaged by Cochlear for the purposes of this investigation
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Pregnant or breastfeeding women
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Currently participating, or participated within the last 30 days, in another interventional clinical investigation/trial involving an investigational drug or device.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | Stanford University | Palo Alto | California | United States | 94304 |
| 2 | Rocky Mountain Ear Center | Englewood | Colorado | United States | 80113 |
| 3 | University of Iowa | Iowa City | Iowa | United States | 52242 |
| 4 | New York Eye and Ear Infirmary | New York | New York | United States | 10003 |
| 5 | University of North Carolina | Chapel Hill | North Carolina | United States | 27517 |
| 6 | Nationwide Children's Hospital | Columbus | Ohio | United States | 43205 |
| 7 | University of Texas Southwestern Medical Center- Department of Otolaryngology Head and Neck Surgery | Dallas | Texas | United States | 75390 |
| 8 | Virginia Mason Medical Center | Seattle | Washington | United States | 98101 |
Sponsors and Collaborators
- Cochlear
- NAMSA
Investigators
- Study Director: Jillian Crosson, Cochlear
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- CAM5816