Temporomandibular Joint Dysfunction Syndrome
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Volunteers who have temporomandibular pain lasting more than 06 months; Who have a permanent dentition with at least 28 permanent teeth; Without periodontitis
Exclusion criteria
Exclusion criteria: Volunteers who have already suffered craniofacial trauma; who have performed previous surgery on the affected temporomandibular joint, rheumatic diseases; volunteers who use analgesics; anti-inflammatory; patients with neurological or cognitive deficits, and who have contraindications to diacutaneous fibrolysis (wounds or skin disorders in the TMJ region, vascular changes, receiving anticoagulant treatment)
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find improvement in the perceived and measured intensity of pain, range of mouth opening, functional status and muscle activation amplitude (electromyography) of women with TMD undergoing diacutaneous fibrolysis treatment | — |
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Countries
Brazil
Contacts
Universidade Federal de Juiz de Fora