aser in Temporomandibular Disorders

Not Applicable

• Conditions: Temporomandibular Joint Disorders; Temporomandibular Joint Dysfunction Syndrome; C05.500.607.221.897; C05.500.607.221.897.897

• Registration Number: RBR-4wt6fw
• Lead Sponsor: niversidade Luterana do Brasil

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Study Start: 2017-11-22
• Last Update Posted: 29 May 2023

Recruitment & Eligibility

• Status: Recruitment completed
• Sex: Not specified
• Target Recruitment: Not specified

Inclusion Criteria

Patients with diagnosis of Temporomandibular Disorders.

Exclusion Criteria

Patients using drugs to control pain; conditions in which the use of laser therapy, such as infection and tumors, is contraindicated; patients using orthodontic appliance or dental prosthesis.

Study & Design

• Study Type: Intervention
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Reduction of joint pain assessed through the Visual Analog Pain Scale (VAS) from pre-post-intervention assessments

Secondary Outcome Measures

Name	Time	Method
Improvement of joint mobility assessed through biophotogrammetry from pre-post-intervention assessments.