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Efficacy of Laser on therapy of Temporomandibular Disorders in individuals with Headaches

Efficacy of Low-Level Laser on therapy of Temporomandibular Disorders in individuals diagnosed with Primary Headaches

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
REBEC
Registry ID
RBR-2n6c247
Enrollment
Unknown
Registered
2026-01-26
Start date
2026-02-02
Completion date
Unknown
Last updated
2026-02-02

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

Conditions

Temporomandibular Joint Disorders

Interventions

This is a randomized, controlled, double-blind clinical trial. A total of eighty-eight participants diagnosed with primary headaches will be randomly allocated to one of two groups, previously organiz
Group 4J will receive four Joules per square centimeter per point
Group 6J will receive six Joules per square centimeter per point
and Group 9J will receive nine Joules per square centimeter per point. Participants will be reassessed 1 month after the end of treatment by an evaluator who did not have access to any stage of the in

Sponsors

Universidade Federal do Delta do Parnaíba
Lead Sponsor
Universidade Federal do Delta do Parnaíba
Collaborator

Eligibility

Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: Individuals between the ages of 18 and 65, regardless of gender; Be Brazilian; Have a diagnosis of primary headache according to the third edition of the International Classification of Headache Disorders Agree to answer all survey questionnaires and undergo the necessary treatments for the proposed duration

Exclusion criteria

Exclusion criteria: Individuals with a history of tumors and neuronal involvement; Diagnosis of Temporomandibular disorders concomitant with pain of odontogenic, neuropathic, and/or tumoral origin; Individuals diagnosed with non-painful Temporomandibular disorder; Pregnant women; Individuals with missing front teeth or dentures, making it impossible to measure maximum mouth opening by measuring the distance between the upper and lower incisors

Design outcomes

Primary

MeasureTime frame
Improvements are expected in pain intensity (assessed by the Visual Analog Scale - VAS), maximum mouth opening (assessed by the interincisal distance in millimeters), and headache impact (assessed by the Headache Impact Test HIIT-6). Data will be collected at baseline, at the end, and four weeks after low-level laser therapy intervention

Secondary

MeasureTime frame
Intends to evaluate the degree of effectiveness of different doses of low-power laser on pain intensity and maximum mouth opening after 4 weeks of intervention

Countries

Brazil

Contacts

Public ContactCaroline do Nascimento

Universidade Federal do Delta do Parnaíba

carolinecostaodonto@yahoo.com.br+55 (86)99990-7182

Outcome results

None listed

Source: REBEC (via WHO ICTRP) · Data processed: Feb 7, 2026