Sound waves in the ear: a new hope for tinnitus?
NCT ID NCT07291648
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether people with tinnitus can tell if they are receiving real or fake ultrasound stimulation of the vagus nerve in the ear. Twenty adults with constant tinnitus for at least six months took part. The goal was to see how well the blinding worked and what side effects occurred, not to measure tinnitus relief. The device, called ZenBud, uses focused ultrasound to stimulate the nerve, which may help normalize brain activity linked to tinnitus.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Ultrasound Vagus Nerve Stimulation (U-VNS) using the ZenBud device
- What this could lead to
- If this approach works, it could point toward a non-invasive, targeted treatment for tinnitus that avoids the side effects of electrical stimulation.
- What could go wrong
- This is a very small, early-stage study (20 people) focused on blinding and side effects, not on whether the treatment actually reduces tinnitus. The device may not prove effective in larger trials.
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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20 people
The number who actually took part.
- Started
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Sep 2025
- Finished
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Jan 2026
- 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.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Aged 18 years or over * Has experienced constant idiopathic tinnitus for at least 6 months * Participant is willing and able to give informed consent for participation in the study * Not currently taking any medication (except the contraceptive pill) * Able and willing to remove any piercings in the left ear Exclusion Criteria: * Current or past diagnosis of a neurological or psychiatric condition * Current or past diagnosis of cardiac arrhythmia * No tinnitus * Has tinnitus, but it is objective, intermittent or onset is less than 6 months ago * Use of medication or recreational drugs that affect the nervous system in the past 3 months * Currently pregnant * Allergy to aquasonic gel or any of its components (propylene glycol, glycerin, isothiazolinones) * Having taken part in a research study in the last 3 months involving invasive procedures or an inconvenience allowance (this must remain for ALL UoN FMHS UREC approved studies)
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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
-
University of Nottingham
Nottingham, United Kingdom
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Other studies related to the condition(s) this trial covers.
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