Clin2
NCT07778641Worth exploringNot yet recruiting

Genetic study for inherited auditory neuropathy hearing loss

Auditory Neuropathy Spectrum DisorderAuditory Neuropathy

Part of Brain & nervous system, Ear, nose & throat clinical trials.

This study looks at a specific genetic cause of hearing loss called OTOF-related auditory neuropathy. If you have this condition, researchers will test your DNA to learn more about it, which may help with future diagnosis and treatment.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
30 people
Ages
Any age
Study type
Observational

Who can take part

  • You have hearing loss that was present from birth or early childhood.
  • You have been diagnosed with auditory neuropathy spectrum disorder (ANSD) – a type of hearing loss where sound reaches the ear but the signal is not sent properly to the brain.
  • Your hearing test (ABR) shows missing or abnormal brain wave responses, and other tests (OAE or CM) show that the inner ear works, which points to ANSD.
  • You have no known cause for the hearing loss, such as premature birth, low oxygen, severe jaundice, or a known syndrome.
  • You have not had cochlear implants in both ears, and there is no structural problem in your inner ear or hearing nerve.

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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