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Can a gentle electrical patch ease jaw pain faster?

NCT ID NCT07744893

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting
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 This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Aug 04, 2026 · Last updated Aug 05, 2026 · Updated 1 time

Summary

This trial tests whether adding transcutaneous electrical nerve stimulation (TENS) to standard care—education, medication, and exercises—provides extra pain relief and better jaw function for people with temporomandibular disorders (TMD). About 48 adults with TMD will receive either standard care alone or standard care plus TENS. The study measures pain at rest and during jaw movement, as well as quality of life, over the short and medium term.

What this could mean

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

Active substance
Transcutaneous electrical nerve stimulation (TENS) added to standard conservative therapy (education, medication, and exercises)
What this could lead to
If effective, adding TENS to standard care could offer faster and better pain relief and improved jaw function for people with temporomandibular disorders.
What could go wrong
This is a small, early-stage trial, and the added benefit of TENS over standard care alone is uncertain. Results may not apply to all TMD patients.

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

48 people

The number who actually took part.

Started

Apr 2011

Finished

May 2013

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: * Patients aged between 18 and 65 years. * Patients diagnosed with temporomandibular disorders (TMD) according to the Research Diagnostic Criteria for Temporomandibular Disorders (RDC/TMD) Axis I. * Patients who agreed to participate and signed the informed consent form. Exclusion Criteria: * Facial pain attributable to another condition (sinusitis, migraine, tension-type headache, trigeminal neuralgia). * TMJ involvement secondary to an inflammatory systemic disease. * TMJ subluxation. * Degenerative cervical disease restricting neck movement. * Any contraindication to TENS.

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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

  • Necmettin Erbakan University

    Konya, Konya, 42090, Turkey (Türkiye)

More trials for these conditions

Other studies related to the condition(s) this trial covers.