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Comparison of the effect of diode laser with transcranial direct current stimulation(TDCS) in reducing symptoms in patients with temporomandibular disorders (TMD)

Comparison of the effect of diode laser with transcranial direct current stimulation(TDCS) in reducing symptoms in patients with temporomandibular disorders (TMD)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20210321050751N3
Enrollment
34
Registered
2022-09-27
Start date
2022-11-22
Completion date
Unknown
Last updated
2022-11-21

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

Conditions

Temporomandibular joint disorders (TMD). Temporomandibular joint disorders

Interventions

Intervention 1: Intervention group: In the laser group, 9 sessions of laser therapy using diode laser ( 980 nm, 100 mW) will be performed during 3 weeks (3 times a week).The diode laser is applied in

Sponsors

Yazd University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 40 Years

Inclusion criteria

Inclusion criteria: 1) Patients 40-18 years old 2) Have vague or obvious pain in the temporomandibular joint for at least 2 months (score 4 or higher on the VAS scale). 3) Have at least one of the following two symptoms.1. Sensitivity to the touch of one or more masticatory muscles2. Mandibular restriction on opening 4) Fill in the informed consent of the patient to enter the study 5) Do not have a history of jaw trauma. 6) Do not have a history of joint disease and rheumatoid arthritis. 7) Do not currently be treated for TMD.

Exclusion criteria

Exclusion criteria: 1. Any illness or trauma that occurs after the start of the study for the samples and affects the rate of TMD symptoms. 2.Taking drugs such as cartilage-building drugs and Nsaid 3.Lack of cooperation in continuing the study to complete the treatment sessions

Design outcomes

Primary

MeasureTime frame
Pain score changes. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: VAS.;Masticatory muscle tenderness changes. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: 1?2?3?4.;Changes in the range of maximum mouth opening. Timepoint: Before treatment, 1 and 3 months after treatment. Method of measurement: mm.

Secondary

MeasureTime frame
Patient satisfaction score of treatment. Timepoint: after treatment. Method of measurement: questionnaire, Contains questions about improving function, jaw sounds, sleep disorders, etc. after treatment.

Countries

Iran (Islamic Republic of)

Contacts

Public ContactParisa Mohsenzade

Yazd University of Medical Sciences

p.mzade75tums@gmail.com+98 34 3428 4157

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026