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The effects of routine treatment and manual therapy in people with temporomandibular disorder

Not Applicable
Conditions
Temporomandibular dysfunction.
Temporomandibular joint disorders
M26.6
Registration Number
IRCT20190621043964N1
Lead Sponsor
Iran University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
All
Target Recruitment
30
Inclusion Criteria

Individuals with tunilateral or bilateral TMD according to the DC/TMD
pain more than 3 based on visual analog scale

Exclusion Criteria

traumatic injury that caused the symptoms in the temporomandibular joint and the orofacial region during the last three months
history of the orofacial surgery during the last 6 months
neurological and systemic diseases such as rheumatoid arthritis; Parkinson; multiple sclerosis, positional vertigo, pregnancy, and severe deformity in the jaw or face region

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Pain. Timepoint: At the baseline, after the end of the treatment, and after a one-month follow-up period. Method of measurement: Visual analog scale.
Secondary Outcome Measures
NameTimeMethod
Maximum mouth opening. Timepoint: At the baseline, after the end of the treatment, and after a one-month follow-up period. Method of measurement: caliper.;Cervical flexion and extension ROM. Timepoint: At the baseline, after the end of the treatment, and after a one-month follow-up period. Method of measurement: Goniometer.
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