Laser treatment for temporomandibular disorder: a randomized controlled clinical trial
- PMID: 40643712
- DOI: 10.1007/s10103-025-04565-x
Laser treatment for temporomandibular disorder: a randomized controlled clinical trial
Abstract
This study aimed to assess the impact of photobiomodulation therapy (PBMT) using low-level laser therapy, an occlusal splint (OS), and their combined application (OSL) on symptoms of muscular temporomandibular disorder (TMD) through a randomized clinical trial. Participants diagnosed with muscular TMD following the Diagnostic Criteria for TMD guidelines were allocated to three groups: OS, L, and OSL. The OS and OSL groups utilized the device during sleep, while PBMT (3 J/cm² per point) was applied to the L and OSL groups in 5 weekly sessions employing infrared light (808 nm). Pain levels were evaluated using the visual analogue scale (VAS), mandibular mobility was assessed via maximum unassisted mouth opening, and quality of life was measured using the Oral Health Impact Profile (OHIP-14). A total of 99 participants (OS: n = 34, L: n = 32, OSL: n = 33), including 80 women and 19 men with an average age of 31.54 ± 10.39 years, were enrolled. Significant pain reduction occurred in the L and OSL groups (p < 0.05), with the OSL group demonstrating higher effectiveness compared to the OS group within the initial two weeks (p < 0.05). Post-treatment, the L and OSL groups exhibited notable improvements in mandibular mobility, except during the final session (p < 0.05). All groups reported enhanced quality of life, with the L group achieving higher scores than the OS and OSL groups during reassessment (p < 0.05). Laser therapy effectively treated muscular TMD, both as a standalone therapy and in combination with the OS, particularly for immediate pain relief. The combination of therapies was important for maintaining stable symptom control over time.
Keywords: Conservative treatment; Low-level laser therapy; Occlusal splint; Quality of life; Temporomandibular joint disorder.
© 2025. The Author(s), under exclusive licence to Springer-Verlag London Ltd., part of Springer Nature.
Conflict of interest statement
Declarations. Ethical approval: The protocol was approved by the study institution’s Human Subjects Research Ethics Committee (opinion no. 66265922.7.0000.5142) and registered on Plataforma Brasil (CAAE: 66265922.7.0000.5142). The present study was described following the CONSORT guidelines for randomized trials (NCT05989217 Clinical Trials Protocol registration). Consent to participate: After being informed about all the research details, all participants signed the Free and Informed Consent Form, as required by the Brazilian National Board of Health. In this manuscript, no individual data or information that could identify any of the participants were reported. Conflict of interest: The authors declare that they have no conflict of interest.
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