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New Generation Low Level Laser Effect in Myofacial Pain Syndrome

U

University of Gaziantep

Status

Completed

Conditions

Myofascial Pain Syndrome

Treatments

Device: Nd:YAG laser
Device: GRR laser

Study type

Interventional

Funder types

Other

Identifiers

NCT06442553
KARAGOZOGLUI

Details and patient eligibility

About

Low level laser treatments have been used to treat painful trigger points in myofascial pain syndrome (MPS), but the effectiveness of the appropriate laser type and parameters is still uncertain. The aim of this study was to compare the effectiveness of different types of low level laser treatment (LLLT) in reducing pain levels, changing oxygen saturation and bite force in patients with MPS.

Full description

A total of 45 patients with MPS were randomly divided into three groups. First group received LLLT with GRR laser over massater muscle region. Patients in the second group were treated with Nd:YAG laser and the same protocol with Nd:YAG laser was performed in the placebo group using sham device. Pain was evaluated by visual analogue scale (VAS), change in oxygen concentration in the massater muscle was measured by functional near-infrared spectroscopy- fNIRS and bite force was measured with Flexiforce sensors before and after treatment.

Enrollment

45 patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

-patients with symptoms of temporomandibular disorders and diagnosed with MPS as a result of the clinical examination.

Exclusion criteria

  • Patients with internal TMJ irregularities or degenerative joint changes,
  • patients with restricted mouth opening, deviation or deflection,
  • patients with systemic diseases,
  • pregnant women,
  • patients who had received MPS treatment within the previous year

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Factorial Assignment

Masking

None (Open label)

45 participants in 3 patient groups, including a placebo group

GRR laser
Experimental group
Description:
patients received 15 sessions GRR laser treatment for 3 weeks
Treatment:
Device: GRR laser
Nd:YAG Laser
Experimental group
Description:
patients received 10 sessions Nd:YAG laser treatment for 2 weeks
Treatment:
Device: Nd:YAG laser
placebo
Placebo Comparator group
Description:
patients received 10 sessions emission-free laser treatment for 2 weeks
Treatment:
Device: Nd:YAG laser

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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