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Efficacy of Different Low Level Laser Therapy Sessions

Not Applicable
Completed
Conditions
Myofascial Pain Syndrome
Interventions
Device: 940-nm diode laser / two session
Device: 940-nm diode laser/ three session
Device: 940-nm diode laser / one session
Registration Number
NCT06327204
Lead Sponsor
October 6 University
Brief Summary

Myofascial pain dysfunction syndrome is one of the common causes of non-odontogenic pain in the head and neck region. It accounts for 40-60% of the adult population. Different treatment modalities had been reported to release the trigger point within the muscles of mastication in order to reduce pain and allow recovery of the function.

Detailed Description

Low-level laser therapy has been a research focus in past few years as it provides effective and conservative treatment modality with minimal patient discomfort. LLLT promotes the release of endogenous opioids, enhance tissue repair and cellular respiration, increase vasodilatation and pain relief Recent systematic review and meta-analysis had reported that the available evidence didn't allow clinicians to draw firm conclusions on effective dosage. This study aimed to investigate the effect of different LLLT sessions' number on pain, maximum mouth opening and quality of life in patients with masseter muscle trigger points.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
90
Inclusion Criteria
  1. definite diagnosis of myofascial pain based on the DC/TMD criteria with a referral
  2. presence of one or more trigger points in the masseter muscle
  3. no history of any invasive procedures of the related masseter muscle.
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Exclusion Criteria
  1. any painful conditions affecting the orofacial region
  2. any systemic diseases that could masticatory function (e.g., rheumatoid arthritis and epilepsy)
  3. pregnancy and lactation.
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Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
group II940-nm diode laser / two sessionpatient received two session / week
Group III940-nm diode laser/ three sessionPatient received three session / week
Group I940-nm diode laser / one sessionpatient received one session / week
Primary Outcome Measures
NameTimeMethod
pain score8 weeks

a 10-point visual analogue score

Secondary Outcome Measures
NameTimeMethod
quality of life questioner8 weeks

Oral Health Impact Profile questionnaire (OHIP-14) containing 14 questions divided into seven domains of oral health

maximum mouth opening8 weeks

measuring the interincisal distance between the upper and lower central incisors

Trial Locations

Locations (1)

Faculty of Dentistry, October 6 University

🇪🇬

Cairo, Egypt

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