Atypical Facial Pain
Conditions
Interventions
This is a two-arm, double-blind, randomized controlled clinical study. The sample will consist of volunteers who have had fixed orthodontic braces fitted, who will be randomly allocated via the websit
Sponsors
Instituto de Saúde e Biotecnologia
Instituto de Saúde e Biotecnologia
Eligibility
Age
12 Years to 45 Years
Inclusion criteria
Inclusion criteria: Volunteers starting orthodontic treatment aged between 12 and 45 years; accepting and signing the conditions of the study in accordance with the Informed Consent Form and Assent Form; good general health; absence of caries lesions or periodontal diseases
Exclusion criteria
Exclusion criteria: Use of analgesic or anti-inflammatory medication; fibromyalgia sufferers; volunteers with Temporomandibular Disorder and pregnant women
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is hoped to find an improvement in the range of movement when opening the mouth and in the perceived and measured intensity of pain with the use of diacutaneous fibrolysis in volunteers with orofacial pain following the placement of fixed orthodontic appliances who have undergone this technique. | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes expected | — |
Countries
Brazil
Contacts
Public ContactWilliam Leite
Instituto de Saúde e Biotecnologia
Outcome results
None listed