Evaluation of Performances, Clinical Benefits and Safety of the 'Audiocap' Connected Hearing Rehabilitation Device for Improving Audibility in Hearing-impaired People in the Context of CE Marking - AUDIOCAP-2

Archean Technologies

Status: Enrolling

Conditions: Hearing Loss, Adult-Onset; Hearing Aid

Treatments: Device: Audiocap connected hearing aid; Device: Placebo

Study type: Interventional

Funder types: Industry

Identifiers

NCT07252492

2025-A01026-43

Details and patient eligibility

About

The goal of this clinical trial is the evaluation of performances, clinical benefits and safety of the 'Audiocap' connected hearing rehabilitation device for improving audibility in hearing-impaired people.

The main question it aims to answer is to demonstrate, after one month's use of the Audiocap connected hearing aid, that the audiological gain for the patient is better than with a placebo hearing aid.

Placebo hearing aid is a Audiocap connected hearing aid with a 'NONE' setting (flat frequency response for the patient (equivalent to not wearing hearing aid).

Participants will be first-time hearing aid users, eligible for hearing aid fitting, and adults according to French legislation (18 years and older).

Enrollment: 100 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

1. Subjects presenting one or more of the following criteria: a.Subject with mild to moderate hearing loss (20dB to 50dB average at 500, 1000, 2000, and 4000 Hz) in the better ear according to WHO standards, / b. Subject with a speech reception threshold (SRT) in quiet exceeding 30dB, corresponding to the minimum speech level required to achieve 50% recognition in silence (HAS eligibility criteria for hearing aid reimbursement), / c. Subject with significant degradation of speech intelligibility in noise, defined as a speech-to-noise ratio (SNR) deviation greater than 3dB compared to normative reference values (HAS eligibility criteria for hearing aid reimbursement), / d.Subject with high-frequency hearing loss greater than 30dB from 2000 Hz onwards, associated with a speech reception threshold exceeding 30dB in quiet and/or a significantly degraded speech intelligibility in noise (HAS eligibility criteria for hearing aid reimbursement).
2. Subjects eligible for first hearing aid.
3. Subjects over 18 years of age. French-speaking subjects.

5. Subjects affiliated with a social security scheme. 6. Subjects who are not subject to another medical option, without external pathology and excluding implants.

7. Subjects who have signed an informed consent. 8. Subjects available for the study.

Exclusion criteria

1. Subject deprived of his/her liberty by a judicial or administrative decision
2. Subject with severe psychiatric disorder
3. Subject admitted to a health or social care establishment
4. Subject not able to give consent
5. Adults under guardianship or trusteeship.
6. Subjects with disabling tinnitus that are not suitable for adaptation (THI>56).
7. Subjects eligible for a cochlear implant.
8. Subjects not able to participate in the study according to the investigator.
9. Subjects with acute and chronic suppurative otitis media, congenital ear atresia, or any type of ear discharge.
10. Subjects with congenital atresia of external ear or deformity of any part of the ear canal.
11. Subjects with deafness that is unstable and with a degree of hearing loss often fluctuating.
12. Subjects with persistent headaches, dizziness, earaches, or other symptoms that are not suitable for adaptation.
13. Subjects with sudden onset of hearing loss within the past 3 months, rapid progressive deafness, unilateral hearing loss or other acute ear disease.
14. Subjects with effusion (secretions/ discharge) in the ear and/or frequent purulence (pus).
15. Subjects with central deafness (central nervous system) or non-organic deafness.
16. Subjects with acute otitis extrema and tympanitis.
17. Subjects who are allergic to materials of the device.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Double Blind

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100 participants in 2 patient groups, including a placebo group

Interventional Arm

Active Comparator group

Description:

First period of one month: Audiocap connected hearing aid in a standard interplay path.

Treatment:

Device: Audiocap connected hearing aid

Control Arm

Placebo Comparator group

Description:

First period of one month: Audiocap connected hearing aid with a 'NONE' setting (flat frequency response for the patient (equivalent to not wearing hearing aid) in a standard interplay path.

Treatment:

Device: Placebo