Internal Photobiomodulation For Management Of Temporomandibular Joint Internal Derangement

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age20-40
SponsorNourhan M.Aly

About this trial

Aim of the study was to compare the efficacy of internal versus external photobiomodulation (PBM) in the management of patients with TMJ internal derangements (TMJ-ID).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Painful click at temporomandibular joint (TMJ) area.

Pain at the lateral pterygoid muscle.

Presence of full or nearly full complement of natural teeth with acceptable occlusion

Disqualifiers

Patients who have radiographic evidence of degenerative conditions of TMJ.

Patients under current dental or physical therapy that could affect TMD.

History of recent trauma.

The presence of systemic diseases (i.e. rheumatoid arthritis, osteoarthritis).

Trial design

Design model

Parallel

Treatments tested in this trial

  • External low level laser therapy

    Device

    Patients received 8 sessions of external diode laser (635 nm).

  • Internal low level laser therapy

    Device

    Patients received 8 diode laser (635 nm) sessions applied internally

Treatment groups

50 Participants
are divided into 2 treatment groups
Group A: External low level laser therapyExperimental treatment 1 intervention
Group B: Internal low level laser therapyActive comparator 1 intervention

Trial outcomes

Primary outcomes

1

Pain level assessment using Visual Analogue Scale

All patients will be evaluated subjectively through Visual Analogue Scale (VAS) to clinically assess the pain intensity with ratings between 0 for pain-free and 10 for maximum pain

Time frame
after one month from the last laser session
2

Oral health-related quality of life using OHIP-TMD

Oral health-related quality of life will be assessed using OHIP-TMD, a 22-item temporomandibular disorder-specific version of the Oral Health Impact Profile (OHIP). Each item in the OHIP-TMDs is scored on a Likert scale, often ranging from: 0 (Never) to 4 (Very often). For each respondent, the scores for all 22 items are summed to create a total score. The total score ranges from 0 to 88, where higher scores indicate a greater negative impact on oral health-related quality of life.

Time frame
after one month from the last laser session
3

Maximum mouth opening evaluation using the Miller index

The Miller Index is calculated as a ratio of the observed maximum interincisal distance (distance between the edges of the upper and lower incisors when the mouth is fully open) to the patient's height. This provides a normalized measure of mouth opening relative to body stature. Miller Index= Maximum Interincisal Distance (mm)/Height (cm) Normal Range: A typical Miller Index is around 1.6 to 1.7 mm/cm in healthy individuals. This means that for every centimeter of height, the expected mouth opening is about 1.6 to 1.7 mm. Deviations: * Lower than Normal: May indicate restricted mouth opening (e.g., trismus, TMDs, fibrosis, ankylosis). * Higher than Normal: May occur in conditions involving hypermobility.

Time frame
after one month from the last laser session

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Nourhan M.Aly

Lead sponsor

University of Alexandria

Sponsor institution