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Laser for temporary treatment of pain in the temples, face and neck.

Low laser therapy in palliative care of temporomandibular dysfunction and orofacial and cervical cranial pain

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-9b6mnj
Enrollment
Unknown
Registered
2018-05-21
Start date
2016-10-24
Completion date
Unknown
Last updated
2025-10-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Temporomandibular joint dysfunction syndrome

Interventions

It will be admistred infrared laser (808 nm) with power of 100 mW, 3.0 J per point of irradiation, 30 seconds/point, energy density of 105 J/cm2, shall be administered, considering the beam area of ??
1 point in the middle part and one point in the posterior part
muscle masseter 3 points at the insertion (lower edge of the mandible) and 3 points at the origin (zygomatic arch)
3 points in the temporomandibular joint with 1 point in the anterior part, 1 point in the posterior part and 1 point in the upper part
6 points in the sternocleidomastoid muscle, 2 points at the origin, 2 points at the middle portion and 2 points at the insertion
1 point on the medial pterygoid muscle located internally in the mouth, behind the retro molar trigone. In the intervention group will be applied the laser as described and in the control group will b
Other
E02.594.540

Sponsors

Faculdade de odontologia da Universidade de São Paulo
Lead Sponsor
Faculdade de odontologia da Universidade de São Paulo
Collaborator

Eligibility

Age
18 Years to No maximum

Inclusion criteria

Inclusion criteria: Adult participants of all ages with primary complaint of pain in the temporomandibular joint region and or orofacial and cervical skull region and or limitation of mouth opening will be included

Exclusion criteria

Exclusion criteria: Participants with: congenital problems with Temporomanbibular joint involvement and or orofacial and cervical skull region; neoplastic conditions; history of recent trauma in the orofacial and cervical skull region; any type of temporomandibular dysfunction treatment plaques; functional orthopedic appliances or fixed and or removable orthodontic appliance; syndromes; cleft lip and or palatine; psychiatric disorders; severe heart problems; tooth in severe precarious conditions, such as periodontitis and or indication of endodontic treatment; in use of topical or systemic photo sensitizing medications, pregnant women, skin related problems in the region to be applied the laser.

Design outcomes

Primary

MeasureTime frame
To verify if the use of low level laser therapy diminishes the pain in the region of temporomandibular joint and facial and cervical immediately after the application (discomfort in the trigger points, in the masticatory muscles in static or dynamic examination in the accomplishment of the protrusion movements and right and left laterality). Measured by the visual analogue scale during palpation and mandibular movements.

Secondary

MeasureTime frame
Check if that symptoms related to TMD and facial and cervical pain improve immediately after application of LBP (mouth opening range, mouth opening trajectory range). Measured by using a caliper and ruler.;To verify the duration of the decrease of the pain in the region of temporomandibular joint, facial and cervical caused by the laser therapy, if observed. The data will be obtained by reporting the participant daily based on the visual and analog scale and marked in a standardized form provided by the researcher after the first and second sessions.;Check if there is "clicking" and / or "crackling" the decrease occurs after laser therapy. It will be measured by the researcher during the clinical examination.;Verify if laser therapy improves quality of life. It will be measured by decreasing the score obtained at the beginning and at the end of the laser therapy. This information will be obtained with the application of the OHIP-14 (Oral Health Impact Profile) questionnaire that will be applied at the beginning and after the third laser therapy session.;To verify if the laser therapy improves the perception of the quality of sleep. It will be measured by decreasing the score obtained at the beginning and at the end of the laser therapy. This information will be obtained with the application of the Epworth scale, which will be applied at the beginning and after the third laser therapy session.

Countries

Brazil

Contacts

Public ContactPatricia Freitas

Faculdade de odontologia da Universidade de São Paulo

pfreitas@usp.br+55(11) 3091-7418

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 21, 2026