Can a 40 hz burst of sound silence tinnitus?
NCT ID NCT06646302
First seen Jun 25, 2026 · Last updated Jun 26, 2026 · Updated 1 time
Summary
This study tested whether a special 40 Hz burst of sound can provide longer-lasting relief from tinnitus (ringing in the ears) compared to standard continuous sound therapy. Researchers enrolled 265 adults with chronic tinnitus and used EEG to measure brain activity changes. The goal is to find a more effective way to temporarily suppress tinnitus and understand how the brain responds.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Personalized 40 Hz broadband or pure tone acoustic stimulation
- What this could lead to
- If successful, this could lead to a more effective, personalized sound therapy for temporary tinnitus relief.
- What could go wrong
- This is a small, early-phase study with no control group, so results may not generalize. The relief is temporary and may not work for everyone.
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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265 people
The number who actually took part.
- Started
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Oct 2024
- Finished
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Jul 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 70 years
- 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: 1. Diagnosed with subjective tinnitus; 2. Chronic tinnitus: tinnitus course ≥ 1 month; 3. Normal middle ear function; 4. The average hearing threshold (defined as mean of 0.5, 1, 2, and 4 kHz) of the unaffected ear \< 60 dB; 5. Tinnitus can be heard under normal circumstances. 6. Subjects are able to understand the purpose of the study, volunteer to participate and cooperate with the instructors to complete the experiment, and be willing to sign the informed consent. Exclusion Criteria: 1. Acute phase tinnitus; 2. Fluctuating tinnitus loudness; 3. Severe psychiatric disorders; 4. Inability to complete tinnitus testing; 5. Fluctuating or retrocochlear hearing loss; 6. Conductive hearing loss; 7. Currently participating in other research projects that may affect tinnitus; 8. Subjects who are not considered suitable for this clinical trial by the researchers.
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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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Eye & ENT Hospital of Fudan University
Shanghai, Shanghai Municipality, 200031, China
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Other studies related to the condition(s) this trial covers.
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