Scientists hunt for tinnitus fingerprint in the brain
NCT ID NCT06520865
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study looked for a measurable brain signal (biomarker) that could objectively diagnose chronic tinnitus. Researchers used EEG to record brain activity in 560 adults—some with constant tinnitus and some without. The goal is to replace trial-and-error diagnosis with a personalized, data-driven tool that is easy to use in clinics.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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560 people
The number who actually took part.
- Started
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Aug 2024
- Finished
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Nov 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.
Who is studied
Patients who have been diagnosed with chronic tinnitus (for at least 6 months) and control subjects who have never had (except short-term) tinnitus.
- Ages
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18 to 70 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
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: (1) for tinnitus cases: a diagnosis of chronic and constant tinnitus (for at least 6 months based on history) * (2) for controls: never experienced tinnitus * (3) age 18 -70; * (4) ability to understand and consent to the research; * (5) ability to participate (hearing ability); * (6) MoCa Test ≥ 26; * (7) hyperacusis questionnaire score \< 27; Exclusion Criteria: * (1) objective tinnitus; heartbeat-synchronous tinnitus as primary complaint; * (2) otosclerosis; acoustic neuroma or other relevant ear disorders with fluctuating hearing; * (3) acute ear nose and throat infections (acute otitis media, otitis externa, acute sinusitis); * (4) Meniere's disease or similar syndromes; * (5) vestibular migraine; * (6) serious internal, neurological or psychiatric conditions; * (7) epilepsy or other CNS disorders (brain tumor, encephalitis); * (8) clinically relevant drug, medication or alcohol abuse up to 12 weeks before study start; * (9) change in anti-depressants/drugs ≤ 2 weeks * (10) missing written informed consent * (11) severe hearing loss - inability to communicate properly in the course of the study; * (12) one deaf ear;
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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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Brai3n - Research center for Advanced, International, Innovative and Interdisciplinary Neuromodulation
Ghent, 9000, Belgium
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Center of Neuromodulation - Psychiatry und Psychotherapie der Universität Regensburg am Bezirksklinikum
Regensburg, Bavaria, 93053, Germany
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OST - Eastern Switzerland University of Applied Sciences
Sankt Gallen, 9000, Switzerland
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Trinity College Dublin
Dublin, Ireland
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University of Illinois
Champaign, Illinois, 61820, United States
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University of Texas
Austin, Texas, 78712, United States
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University of Tuebingen
Tübingen, Baden-Wurttemberg, 72074, Germany
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Other studies related to the condition(s) this trial covers.
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