A Prospective, Open-label, Pivotal Study to Assess Spectacle Hearing Aid Safety and Efficacy

Trial statusRecruiting
Trial phasePhase 2, Phase 3
Trial typeInterventional
Biological sexAll
Age18+
SponsorNuance Hearing

About this trial

Following informed consent signature and upon verification of eligibility and execution of informed consent, subjects will be assigned a study code. The study comprises two groups. Screening visit will be conducted for both groups and include hearing test battery to assess hearing aid safety and efficacy

Eligibility criteria

Qualifiers

Adults aged 18 years and older

Perceived mild to moderate hearing loss as indicated by at least 1 positive answer to any of the signs specified by FDA: a) You have trouble hearing speech in noisy places, b) You find it hard to follow speech in groups, c) You have trouble hearing on the phone. d) Listening makes youtired, e) You need to turn up the volume on the TV or radio, and other people complain it's too loud

Wearing corrective glasses for daily use

Cognitive ability to understand and follow study instructions.

Disqualifiers

Hearing loss >55 dB HL

Prior hearing aid usages for the last 12 months

Medical history of cognitive or neurological impairment.

Active inflammatory conditions affecting the ear

Trial design

Treatments tested in this trial

  • Spectacle Hearing Aid

Treatment groups

89 Participants
are divided into 1 treatment group

Sponsors and collaborators

Nuance Hearing

Lead sponsor

Assuta Medical Center

Collaborator