Pupil dilation may reveal secrets of hearing nerve
NCT ID NCT05870527
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looks at how stimulating a nerve in the ear affects pupil size during cochlear implant surgery. Researchers will measure pupil dilation in 30 adults to learn more about the vagus nerve's role in hearing. The goal is to gather knowledge, not to treat hearing loss directly.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Electrical stimulator
- What this could lead to
- If successful, this could help doctors better understand how the vagus nerve affects hearing, potentially improving cochlear implant outcomes.
- What could go wrong
- This is a very small, early study with only 30 participants, focused on measuring pupil size rather than treating hearing loss. It may not lead to any direct benefit for patients.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jul 2023
- Expected to finish
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Jun 2026
An estimate. End dates often move.
- 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: Patients undergoing cochlear implantation: * will be undergoing surgery for a cochlear implant * is over the age of 18 * is willing to participate in the study Patients undergoing vagal nerve stimulator implantation: * will be undergoing implantable vagal nerve stimulation * is over the age of 18 * is willing to participate in the study Exclusion Criteria: Patients undergoing cochlear implantation: * is under the age of 18 * has history of prior ear surgery, congenital ear malformation, or cochlear implantation * pregnant or breastfeeding patients cannot undergo the standard-of-care implantation procedures required for participation in the study. * medical comorbidities resulting in exclusion are guided by the AANS exclusion criteria for VNS and include the following: * One vagus nerve * Receiving other concurrent forms of brain stimulation * Heart arrhythmias or other heart abnormalities * Dysautonomias (abnormal functioning of the autonomic nervous system) * Lung diseases or disorders (shortness of breath, asthma, etc.) * Ulcers (gastric, duodenal, etc.) * Vasovagal syncope (fainting) * Pre-existing hoarseness Patients undergoing vagal nerve stimulator implantation: * is under the age of 18 * has history of prior ear surgery, congenital ear malformation, or cochlear implantation * pregnant or breastfeeding * medical comorbidities resulting in exclusion are guided by the AANS exclusion criteria for VNS and include the following: * One vagus nerve * Receiving other concurrent forms of brain stimulation * Heart arrhythmias or other heart abnormalities * Dysautonomias (abnormal functioning of the autonomic nervous system) * Lung diseases or disorders (shortness of breath, asthma, etc.) * Ulcers (gastric, duodenal, etc.) * Vasovagal syncope (fainting) * Pre-existing hoarseness
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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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.
Contacts and locations
Locations
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NYU Langone Health
New York, New York, 10016, United States
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