Paresis
Conditions
Interventions
The clinical trial is a single-group interventional study with thirty (30) patients undergoing oral and maxillofacial surgery who will be divided into two groups according to the type of injury/surger
E02.594.540
Sponsors
Centro Universitário Serra dos Órgãos
Universidade Federal Fluminense
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Healthy volunteers will be included in the research; both genders; age between 18 and 60 years old; indispensability of surgical treatment through oral and maxillofacial surgery; with sensory and/or motor changes in the face; patients who signed and agreed to the consent form
Exclusion criteria
Exclusion criteria: Patients who do not require a surgical approach, who refuse to participate in the research, patients with facial PAN fractures, orthognathic surgery patients and also patients with bilateral facial fractures will be excluded from the research
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| It is expected to find a significant improvement in the nerve regeneration of patients treated surgically by the oral and maxillofacial surgery team, through the visual analogue scale and the mechanoreceptor test, carried out using a soft bristle brush. It is understood that the use of laser therapy can increase the patient's neurosensory response by 20% | — |
Secondary
| Measure | Time frame |
|---|---|
| It is expected to verify which facial sensory nerve responded best to the therapy performed | — |
Countries
Brazil
Contacts
Public ContactRaissa Fares
Centro Universitário Serra dos Órgãos
Outcome results
None listed