Den här översättningen är inte klar ännu. Den här sidan är just nu på engelska.

Gå till den engelska sidan

Jaw pain study: which simple therapy works best?

NCT ID NCT05989217

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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tested five different non-surgical treatments for jaw joint (TMJ) pain in 160 adults. Treatments included a mouthguard, low-level laser therapy, laser acupuncture, or combinations of these. The goal was to see which approach best reduced pain and improved mouth opening over four weeks.

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

160 people

The number who actually took part.

Started

Mar 2023

Finished

Jan 2025

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 years and older

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: * Adults of legal age * Both sexes * Regardless of race or social class * With the main complaint of pain in the temporomandibular joint or orofacial region * With or without limitation of mouth opening, diagnosed through the DC/TMD axis1, with pain in the masticatory mm and muscular TMD * Participants must have complete permanent dentition and normal occlusion. Exclusion Criteria: * Congenital problems affecting the TMJ and/or orofacial and cervical region of the skull; * Neoplastic conditions; * History of recent trauma to the orofacial/cervical region of the skull; * Previous use of any type of TMD treatment plate; * Current use of functional orthopedic appliances or fixed and/or removable orthodontic appliances; * Cleft lip and/or palate syndromes; * Psychiatric disorders; * Severe cardiac problems; * A severely poor dental condition such as periodontitis and/or indication for endodontic treatment; * Those using topical or systemic photosensitizing drugs; * Pregnant women; * Dermatological diseases in the region where irradiation will be performed; * Patients with impaired cognitive ability; * History of head trauma related to the etiology of orofacial pain; * Migraine or intracranial disorders; * Who used medications in the last 3 months that may interfere with the effect of therapies, such as relaxants, anticonvulsants and who used medications to treat TMD or muscular pain; * Who had other causes of orofacial pain, such as caries, neuropathies and fibromyalgia; * Who had phobia about needles or bleeding disorders; * Patients who are unable to attend the clinic during the prescribed treatment period; * Patient who insists on a specific treatment (e.g. occlusal adjustments, medication); * Presence of removable full or partial dentures with distal extension.

Get updates

Get notified about this study

Sign up to get updates when this study changes or when new studies for Photobiomodulation are added.

Vår säkerhetsrekommendation!

Genom att skicka in godkänner du våra Användarvillkor

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

  • Universidade Federal de Alfenas

    Alfenas, Minas Gerais, 37130001, Brazil

More trials for these conditions

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