Can a light beam ease jaw pain? laser therapy put to the test in TMD
NCT ID NCT07840495
First seen Sep 25, 2026 ยท Last updated Sep 25, 2026
Summary
Researchers are testing whether low-level laser therapy, added to standard care, reduces jaw pain and improves movement in adults with temporomandibular disorders. Participants receive either an active laser or a sham laser on tender jaw points during six sessions over two weeks, alongside ibuprofen, muscle relaxants, moist heat, and a soft diet. The trial measures pain during muscle palpation and jaw movements, plus how wide participants can open their mouths, at baseline, after each session, and at follow-up visits.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- low-level laser therapy (LLLT)
- What this could lead to
- If it works, low-level laser therapy could become a drug-free add-on that helps people with jaw pain move and eat more comfortably.
- What could go wrong
- The trial is small, with 30 participants, and uses a sham laser for comparison. Laser therapy may add little beyond standard care, and results in this group may not apply to everyone with TMD.
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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
-
30 people
The number who actually took part.
- Started
-
Jan 2024
- Finished
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Aug 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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
-
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. Patients aged 18 and above 2. Patients diagnosed with TMD utilizing Axis I of the DC/TMD 3. Patients diagnosed with TMD irrespective of the severity as screened utilizing the Fonseca Anamnestic Index (FAI) questionnaire form (APPENDIX D) 4. American Association of Anesthesiologists (ASA) Physical Status Classification I-II 5. Class I occlusion/malocclusion 6. Natural dentition patient with at least one pair of occluding posterior teeth on each side of the mandible Exclusion Criteria: 1. Patients who refuse participation/do not consent to the study 2. Patients presenting with any lesion or pathology over the TMJ region 3. Patients presented with TMD-like signs and symptoms secondary to non-TMJ origin (pain or infection of odontogenic origin, ear origin, neuralgia, migraine, atypical facial pain, etc.) 4. Patients that are presented with active infection involving the orofacial region 5. Patients with psychiatric and neurological disorders as confirmed by medical practitioners. 6. Patients with systemic or autoimmune disorders affecting the masticatory system, bones, and joints (rheumatoid arthritis, osteoarthritis) 7. Patients that are contraindicated for the use of LLLT (malignant disease, ongoing radiotherapy, thyroid gland disease, epilepsy, light sensitivity, hemophilia, and other blood and clotting diseases, etc.) 8. TMD patients receiving physical or psychological treatment, and those who have been using muscle relaxants, anti-inflammatory agents (for at least seven days before study begins) or an occlusal appliance 9. Patients with a history of facial bone fractures 10. Patients on fixed orthodontic appliances, history of orthognathic surgery, or TMJ surgery 11. Patients with occlusal interferences, removable partial or total denture wearers, and fixed prostheses that are affecting patients' occlusion 12. Patients with an allergy to, or contraindication for, the use of NSAIDs 13. Pregnant patients
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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
-
Faculty of Dentistry, Universiti Malaya, Malaysia
Kuala Lumpur, Kuala Lumpur, 50603, Malaysia
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