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Development of a Battery of Audiological Tests for the Precision Diagnosis of Age-related Hearing Loss (AUDIOGENAGE)

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Pasteur Institute

Status

Enrolling

Conditions

Presbyacusis

Treatments

Other: Audiological and vestibular tests
Other: neurocognitive self-questionnaire
Other: Blood sampling

Study type

Interventional

Funder types

Industry
Other

Identifiers

NCT05312983
2021-A02543-38 (Other Identifier)
2021-062

Details and patient eligibility

About

Age-related hearing loss, or presbycusis, is caused by many genetic and environmental factors. Its prevalence poses a public health challenge of early identification and effective hearing aid treatment. However, the lack of screening and of a validated audiological test battery to diagnose an individual's needs and to guide hearing aid adjustments is a major obstacle.

Furthermore, monogenic forms of hearing loss affect only one functional module of hearing. The audiological test(s) dependent on the function of this module are affected, in a progressive manner, but not the others. A previous study showed that in early onset presbycusis patients, a quarter of the subjects tested were affected by monogenic presbycusis.

The collection of audiological and vestibular tests, carried out on proven monogenic presbycusis patients and compared to that of normal hearing patients, would constitute a battery of tests allowing a precision diagnosis, then developed to all forms of presbycusis in order to study if the identification of abnormal functional modules can usefully guide the diagnosis and the early fitting.

Full description

The AUDIOGENAGE project is a multi-center, non-invasive case-control study conducted by CERIAH (CEntre de Recherche et d'Innovation en Human Audiology) and LCA (Laboratory de correction auditive) in 700 volunteer participants identified in two groups:

  • 500 Patients with age-related hearing loss of anticipated onset,
  • 200 Control subjects, considered as normal hearing for their age at inclusion.

All participants will undergo 6h audiological and vestibular tests, and also neurocognitive test (self-questionnaire). These tests will be conducted over 2 to 4 visits. A 10 mL-blood sample will be collected for a genetic analysis.

Enrollment

700 estimated patients

Sex

All

Ages

18+ years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

For all participants:

  • Be over the age of 18,
  • Be affiliated to a social security system,
  • Have a good command of the French language (oral and written).

For the group of participants with anticipated presbycusis:

  • Over the age of 40, having a hearing aid recipient or coming for a first hearing aid recipient
  • Between 18 and 40, having a hearing aid recipient, coming for a first hearing aid recipient or declare a progressive genetic birth defect

For healthy volunteers:

  • Have no known hearing loss.

Exclusion criteria

  • Report having been chronically exposed to loud sounds.
  • Have a history of ototoxic substances,
  • To have sequelae of ear infections and/or a history of ENT disease that permanently affects hearing or balance,
  • Have an ethnic origin for which the Pasteur Institute does not have information on the frequency of variants of the genes studied.
  • Have type II diabetes,
  • Have a neurological or psychiatric condition that interferes with comprehension or ability to move,
  • Be under guardianship,
  • Be deprived of liberty by judicial or administrative decision, or be subject to legal protection,
  • Not being subject to a social security system,
  • Taking narcotic substances, alcohol or medication that diminishes cognitive abilities.

Trial design

Primary purpose

Diagnostic

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

700 participants in 1 patient group

people over the age of 18 who agree to participate in the research.
Experimental group
Description:
They are either people who have a hearing loss about 20 years older than their age and wear a hearing aid (or come in for a hearing aid), or people over the age of 40 with normal hearing for their age.
Treatment:
Other: Blood sampling
Other: neurocognitive self-questionnaire
Other: Audiological and vestibular tests

Trial contacts and locations

2

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Central trial contact

Paul Avan, MD; Celine Quinsac

Data sourced from clinicaltrials.gov

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