MedPath

Oral splint and counselling for the treatment of chronic facial pai

Not Applicable
Not yet recruiting
Conditions
Temporomandibular disorder, stress psychological
C05.500.607.221.897
F01.145.126.990
F01.145.126.350
I01.800
Registration Number
RBR-795k8m
Lead Sponsor
niversidade Federal de Juiz de Fora
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
not yet recruiting
Sex
Female
Target Recruitment
Not specified
Inclusion Criteria

All subjects participated in this study volunteers by signing the consent form. Inclusion criteria are as follows:
female subjects;
aged 20 to 55 years;
irrespective of race, social status or religion;
presence of pain intensity of at least moderate (at least 4.0 on VAS), shown in the first clinical assessment;
diagnosis of myofascial pain persisting for a minimum period of six months.

Exclusion Criteria

history of psychiatric disorders or treatment for neurological or psychological disorders;
volunteers with severe intellectual or physical disability that would hinder the collection of data;
history of systemic diseases that generate joint symptoms, muscle or rheumatologic, such as rheumatoid arthritis and fibromyalgia;
pain attributed to a well-defined local cause, such as pulpitis, trigeminal neuralgia and cancer pain;
attributable to migraine pain or infection;
report of any previous treatment for TMD;
treatment with drugs affecting the central nervous system (muscle relaxants, anticonvulsants, opioids, and antidepressants) and treatment with analgesics and anti-inflammatory drugs, with or without prescription, concomitant therapies to be instituted in this research;
report of facial trauma as a possible etiology of TMD;
subject denture wearers an upper or lower;
volunteers aged under 20 or over 55 years;
male individuals.

Study & Design

Study Type
Intervention
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
© Copyright 2025. All Rights Reserved by MedPath