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Internal Photobiomodulation For Management Of Temporomandibular Joint Internal Derangement

Internal Photobiomodulation For Management Of Temporomandibular Joint Internal Derangement: A Randomized Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06763419
Enrollment
50
Registered
2025-01-08
Start date
2024-12-25
Completion date
2025-02-28
Last updated
2025-01-08

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

Conditions

Temporomandibular Joint Disorders

Brief summary

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).

Interventions

DEVICEExternal low level laser therapy

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

DEVICEInternal low level laser therapy

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

Sponsors

Nourhan M.Aly
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
20 Years to 40 Years
Healthy volunteers
No

Inclusion criteria

* 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

Exclusion criteria

* 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). * Pregnant and lactating females. * Presence of open bite.

Design outcomes

Primary

MeasureTime frameDescription
Pain level assessment using Visual Analogue Scaleafter one month from the last laser sessionAll 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
Oral health-related quality of life using OHIP-TMDafter one month from the last laser sessionOral 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.
Maximum mouth opening evaluation using the Miller indexafter one month from the last laser sessionThe 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.

Countries

Egypt

Contacts

Primary ContactMariam Bahgat, PhD
mariam.amin@alexu.edu.eg+20 12 22882107

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026