Cochlear implant boosts hearing in One-Eared hearing loss
NCT ID NCT03052920
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked at whether a cochlear implant in the poorer ear can help adults with hearing loss in one ear who already use a hearing aid in the better ear. Forty adults who had trouble with standard hearing aids received a cochlear implant. Researchers measured word understanding and sound localization before and after the implant. The goal was to see if the implant improves hearing and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- cochlear implant device
- What this could lead to
- If successful, this could show that cochlear implants improve hearing and sound localization for people with hearing loss in one ear.
- What could go wrong
- This is a small, completed study with only 40 participants, so results may not apply to everyone. There are also risks from surgery, such as infection or device failure.
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
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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
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40 people
The number who actually took part.
- Started
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Jul 2017
- Finished
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Mar 2021
- Lead sponsor
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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.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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: * 18 years of age or older * English as the native language * Have a desire for functional binaural hearing * Have failed a previous hearing aid (HA) treatment for asymmetric hearing loss (BiCROS or poor ear HA) or willing to complete a trial if necessary * Willingness to comply with all study requirements * Ability to provide informed consent * Poor ear (ear to be implanted): * Pure-tone average (PTA) at .5, 1 and 2 kilohertz (kHz) \> 70 dB HL (hereafter referred to as severe to profound hearing loss - SPHL) * Aided word recognition score (CNC Word Test) at 60 dB SPL ≤ 30% * Duration of SPHL ≥ 6 months * Onset of hearing loss ≥ 6 years of age * Better ear: * PTA at .5, 1, 2, 4 kHz of 40 to 70 dB HL * Currently using a HA * Aided word recognition score (CNC Word Test) at 60 dB SPL \> 40% * Stable hearing for the previous 1-year period. "Stable" is defined as thresholds that have not changed by more than 10 dB at 2 or more octave interval audiometric frequencies Exclusion Criteria: * Medical condition that contraindicates surgery * Actively using an implantable device in the ear to be implanted * Known cochlear malformation or obstruction that would preclude full insertion of the electrode array in the ear to be implanted * Hearing loss of neural or central origin * Unrealistic expectations related to the benefits and limitations of cochlear implantation * Unwillingness or inability to comply with all investigational requirements
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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
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House Clinic
Los Angeles, California, 90057, United States
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New York University School of Medicine
New York, New York, 10016, United States
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Saint Luke's Midwest Ear Institute
Kansas City, Missouri, 64111, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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Other studies related to the condition(s) this trial covers.
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