Acupuncture needles take on tinnitus: will they silence the noise?
NCT ID NCT07522567
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study tests whether acupuncture can reduce the severity of chronic tinnitus (ringing in the ears) in adults. Researchers will compare 72 tinnitus patients with healthy volunteers, and track changes in symptoms and brain activity after 10 acupuncture sessions. The goal is to see if this ancient practice offers real relief and how it affects hearing pathways.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- acupuncture
- What this could lead to
- If it works, this could provide a safe, non-drug option to reduce tinnitus severity and improve quality of life.
- What could go wrong
- This is a small, early-stage study with no control group for the acupuncture effect, so results may not be conclusive or widely applicable.
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 72 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Dec 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2027
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 to 60 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. Aged between 18 and 60 years, inclusive, any sex; 2. No previous chronic functional or organic diseases, no head injury; 3. No history of any psychiatric or neurological family genetic disease; 4. Signed a paper version of the informed consent form and volunteered to participate in this trial. Exclusion Criteria: 1. Pregnant or breastfeeding women, and those who have a request for childbearing within the last six months; 2. History of head trauma; 3. Presence of metallic implants in the body or any other contraindication to ABR testing; 4. Current participation in any other interventional clinical trial.
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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 official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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.
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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