Efficacy of Red and Infrared Lasers in Treatment of Temporomandibular Disorders
NCT ID: NCT01659840
Last Updated: 2012-08-08
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
116 participants
INTERVENTIONAL
2010-09-30
2010-11-30
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
TRIPLE
Study Groups
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Red laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Red laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Infrared laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Infrared laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Interventions
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Red laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Infrared laser
On the pain points of muscle, laser was applied (8J/cm ²) with an interval of 48 hours between applications. In the joints with sensitivity, a dose of 4J/cm2 laser was applied with an interval of 48 hours between applications.
Eligibility Criteria
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Inclusion Criteria
* Temporomandibular Disorder diagnosed by the Research Diagnostic Criteria for Temporomandibular Disorders questionnaire (RDC);
* pain score ≥ 5 on palpation according to a visual and numerical scale (VNS)
Exclusion Criteria
* patients with previously undergone TMD treatment, or suffered facial trauma
18 Years
60 Years
ALL
Yes
Sponsors
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Federal University of São Paulo
OTHER
Responsible Party
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Olga Flecha
Professor
Principal Investigators
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Olga D Flecha, Professor
Role: PRINCIPAL_INVESTIGATOR
Federal University of the Valleys of Jequitinhonha and Mucuri
Locations
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Periodontics Clinic, Department of Dentistry
Diamantina, Minas Gerais, Brazil
Countries
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Other Identifiers
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senhaodf
Identifier Type: -
Identifier Source: org_study_id