Could a brain zap and white noise silence tinnitus?
NCT ID NCT04551404
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tested whether combining mild electrical brain stimulation (tRNS) with white noise can temporarily reduce tinnitus symptoms. 35 adults with chronic tinnitus received either the combined treatment or brain stimulation alone. Researchers measured changes in tinnitus loudness and distress using rating scales and brain activity recordings.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- transcranial Random Noise Stimulation (tRNS) with acoustic stimulation (white noise)
- What this could lead to
- If it works, this could point toward a non-invasive way to temporarily reduce tinnitus loudness and distress.
- What could go wrong
- This is a small, early-stage study with only 35 people. The effects may be small or not last long, and not everyone may benefit.
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
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35 people
The number who actually took part.
- Started
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Mar 2021
- Finished
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May 2025
- 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 to 75 years
- Sex
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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 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: * Male and female patients 18 years to 75 years of age (younger age limit according to corona virus protection concepts and measures of the FOPH: Schutzkonzepte und -massnahmen (admin.ch)) * Persistent chronic tinnitus with duration of more than 3 months * Signed Informed Consent after being informed about the study * Fluent in German or English * Tinnitus with a THI Grade 2 to 4 (18-76 points) * Willing and able to attend the study visits Exclusion Criteria: * Actual neurological or psychiatric disorders * Hyperacusis * Regular intake of medication influencing the central nervous system (e.g. neuroleptics, hypnotics, sedatives, and anti-epileptics) * Implanted pacemaker * Surgical implants in the head region, such as cochlea implants * Asymmetrical hearing (more than 20dB side difference), pantonal hearing loss \> 40dB in any measured frequency up to 2kHz * Women who are pregnant or breast feeding * Intention to become pregnant during the course of the study * Known or suspected non-compliance, drug or alcohol abuse * Participation in another study with investigational drug within the 30 days preceding and during the present study, * Enrolment of the investigator, his/her family members, employees and other dependent persons
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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 Hospital Zurich, University Zurich
Zurich, Canton of Zurich, 8091, Switzerland
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