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NCT06169683 Clinical Trial

Lyric4 Outcomes Evaluation

Hearing Loss Clinical Trial

Official title:
Evaluation of Daily- and Extended-wear Hearing Instruments

Clinical Trial Details — Status: Active, not recruiting

Administrative data
NCT number NCT06169683
Other study ID # SRF-6569
Secondary ID
Status Active, not recruiting
Phase N/A
First received
Last updated
Start date November 10, 2023
Est. completion date January 2024

Study information
Verified date December 2023
Source Sonova AG
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical investigation is to obtain feedback on Lyric4 device updates within a cohort of experienced adult Lyric hearing instrument users. The main question it aims to answer is: • Do device updates cause a change in Lyric patient experience? Participants will be asked to complete questionnaires about their past experience with Lyric, as well as their experience with Lyric during the study period. They will also be asked to undergo aided audiometric testing with Lyric devices.

Recruitment information / eligibility
Status Active, not recruiting
Enrollment 28
Est. completion date January 2024
Est. primary completion date January 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Experience with Lyric hearing instruments - Willingness to travel to the study site and complete study procedures - Adults, age 18 or older - Fluency with English (written/spoken) Exclusion Criteria: - No Lyric hearing instrument experience - Ear health issues preventing Lyric fitting or requiring medical clearance prior to fitting - Difficulty reading when corrected for vision loss

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• Lyric4
Lyric4 Hearing instrument use

Locations
Country Name City State
United States Triangle Hearing Services Cary North Carolina
United States Sonova Silicon Valley Fremont California

Sponsors (1)
Lead Sponsor Collaborator
Sonova AG

Country where clinical trial is conducted

United States, 

Outcome
Type Measure Description Time frame Safety issue
Primary Aided Audiometric Testing From enrollment to the end of the study period, approximately one month.
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