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Lyric4 Outcomes Evaluation

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Sonova

Status

Active, not recruiting

Conditions

Hearing Loss

Treatments

Device: Lyric4

Study type

Interventional

Funder types

Industry

Identifiers

NCT06169683
SRF-6569

Details and patient eligibility

About

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.

Enrollment

28 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

28 participants in 1 patient group

Experienced Lyric Users
Experimental group
Description:
This cohort of participants is required to have Lyric hearing instrument experience, and they will be asked to wear Lyric for the duration of the study period and report on their experience.
Treatment:
Device: Lyric4

Trial contacts and locations

2

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Data sourced from clinicaltrials.gov

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