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New study aims to take the guesswork out of cochlear implant adjustments

NCT ID NCT07371299

Knowledge-focused Sponsor: Assistance Publique - Hôpitaux de Paris Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether objective measurements, like the stapedius reflex, can help doctors program cochlear implants more precisely. Currently, tuning relies on patients describing what they hear, which can be subjective. Researchers will test 60 adults with severe hearing loss to see if these objective measures match the patient's preferred comfort levels. The goal is to make implant adjustments faster and more reliable.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Participants

About 60 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jan 2026

An estimate. Start dates often move.

Expected to finish

Oct 2029

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Who is studied

Adult patients who are going to receive or have received a cochlear implant.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: Incident case cohort: * Age ≥ 18 years (18 years or older) * Scheduled for first-time unilateral cochlear implantation within the next 3 months * Informed about the study and did not object (non-opposition) Cross-sectional sample of prevalent cases: * Age ≥ 18 years (18 years or older) * Underwent unilateral cochlear implantation more than 1 year ago * Has used the implant for more than 1 year (interval between implantation surgery and study inclusion \> 1 year) * Informed about the study and did not object (non-opposition) Exclusion Criteria: Exclusion Criteria - applies to both the incident case cohort and the cross-sectional sample of prevalent cases: * Prior middle or inner ear surgery * Cognitive impairment or insufficient comprehension of French that would prevent understanding of study procedures or accurate measurement of comfort thresholds during programming * Peripheral facial palsy * Bilateral cochlear implantation * Patient under legal guardianship/court-ordered protection Additional exclusion - cross-sectional sample of prevalent cases only: \- More than half of the electrodes not inserted (i.e., \<50% electrode insertion) Secondary exclusion criteria - Incident case cohort: * More than half of the electrodes not inserted (\<50% electrode insertion) * Postoperative peripheral facial nerve palsy following the implantation surgery

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Conditions

The condition(s) this trial relates to.

sensorineural hearing loss disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Severe to profound sensorineural hearing loss

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  2. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

More trials for these conditions

Other studies related to the condition(s) this trial covers.