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New bluetooth mode aims to improve sound for cochlear implant users

NCT ID NCT07028619

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
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 25, 2026 · Last updated Jun 27, 2026 · Updated 2 times

Summary

This study tested a new bimodal Bluetooth streaming feature for people who use a MED-EL cochlear implant in one ear and a Starkey hearing aid in the other. Ten participants tried the feature for one week and then completed a survey about their listening experience. The goal was to see if the new streaming option improved sound quality and user satisfaction compared to standard Bluetooth streaming.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Bimodal streaming configuration (device feature)
What this could lead to
If successful, this could offer a better wireless streaming experience for people who use both a cochlear implant and a hearing aid.
What could go wrong
This is a very small, completed study with only 10 participants, so results may not apply to everyone. The feature may not work well for all users or devices.

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.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

10 people

The number who actually took part.

Started

Jun 2025

Finished

Sep 2025

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

Who can take part

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

Ages

Children (under 18), adults (18 to 64) and older adults (65 and over)

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: * Implanted with a MED-EL cochlear implant in one ear * Using an AudioKey compatible MED-EL audio processor * Using an AudioKey compatible Starkey hearing aid * If not using a SONNET 3 audio processor, has access to a MED-EL streaming device * Using a smartphone that can support the AudioKey application * Able to complete a survey via cellphone or computer * Prior experience with Bluetooth streaming or expressed motivation to Bluetooth stream to hearing devices * Ability to complete all study procedures including provide responses to survey questions Exclusion Criteria: * Unable to provide reliable feedback * Unable to operate a smartphone with or without assistance

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

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

Contacts and locations

Locations

  • Idaho Ear Clinic

    Meridian, Idaho, 83642, United States

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