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Acupuncture needles take on tinnitus in 180-Patient trial

NCT ID NCT07515482

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether manual acupuncture can reduce the burden of acute tinnitus compared to sham acupuncture or usual care. Researchers will enroll 180 adults with bothersome tinnitus lasting 2 weeks to 6 months. Participants receive 10 sessions over 4 weeks, and outcomes focus on tinnitus-related handicap and function.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
manual acupuncture
What this could lead to
If it works, this could offer a non-drug option to ease tinnitus-related handicap and improve quality of life.
What could go wrong
This is an early-stage trial with no phase, so results may not be conclusive. Sham acupuncture also involves needles, making it hard to separate real from placebo effects.

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

About 180 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Jun 2026

An estimate. Start dates often move.

Expected to finish

Dec 2027

An estimate. End dates often move.

Lead sponsor

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

18 to 65 years

Sex

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

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 18-65 years, male or female; 2. Primary complaint is persistent tinnitus (unilateral or bilateral); 3. Meet the diagnostic criteria for primary tinnitus according to the 2014 Clinical Practice Guideline developed by the American Academy of Otolaryngology-Head and Neck Surgery Foundation (AAO-HNSF); 4. Had continuous tinnitus ≥2 weeks and \<6 months; 5. Tinnitus should be bothersome, with a screening THI score 28-76; 6. Acupuncture naive; 7. Able to provide written informed consent. Exclusion Criteria: 1. Objective tinnitus; 2. Pulsatile tinnitus; 3. Diagnosed as secondary tinnitus as evaluated by audiologists and clinicians(Menière's disease, temporomandibular joint disorder or other diseases); 4. Had evidence of conductive hearing loss (confirmed by abnormal otoscopy or tympanogram); 5. Had contraindications for acupuncture, including curent pregnant, severe anemia, coagulation disorders, etc; 6. Having difficulties in expressing their symptoms clearly( severe mental disorders or cognitive impairment); 7. Currently suffering from other serious acute or chronic organic diseases, such as cerebrovascular, cardiovascular, liver, kidney, hematological diseases, infectious diseases, or malignant tumors; 8. Has received intratympanic injection, postauricular injection, corticosteroids, or other medications for tinnitus treatment (includingTraditional Chinese Medicine or proprietary Chinese medicines) within the past 2 weeks or at baseline; 9. Participated in other clinical trials, particularly those closely related to tinnitus treatment, such as sound therapy; 10. have a strong desire for medication treatment.

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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

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  1. The places running it

    1 site. The list below names each one and where it is.

  2. 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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  3. A doctor treating you

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Contacts and locations

Locations

  • Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology,

    Wuhan, Hubei, 430030, China

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