Dysgeusia
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Tested positive for coronavirus (COVID-19) after the Reverse Transcriptase Reaction followed by Polymerase Chain Reaction (RT-PCR) examination and who complained of symptoms of dysgeusia; Patients aged 18 years or older; Patients who are not in the disease transmission phase (fifteen days after the onset of symptoms); Patients who accept to be part of the research by signing the Free and Informed Consent Term; Patients who underwent gustatory dysfunction assessment tests and dysgeusia was confirmed
Exclusion criteria
Exclusion criteria: Patients who tested negative for coronavirus (COVID-19) after the Reverse Transcriptase Reaction followed by Polymerase Chain Reaction (RT-PCR) test; No complaints of dysgeusia symptoms; Under 18 years old; Pregnant and/or lactating patients; Patients who do not accept to participate in the research or who do not sign the Free and Informed Consent Form
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| It is expected that, with the application of Laser Irradiation of Blood (ILIB) associated with photobiomodulation, there will be a faster reversal of dysgeusia symptoms in the group that will be applied laser therapy compared to the group that will only be simulated with light therapy. The time of dysgeusia reversal in both groups will also be observed. | — |
Primary
| Measure | Time frame |
|---|---|
| It is expected that, with the application of a non-invasive therapy with low intensity laser, which will consist of the systemic photoactivation of the carotid artery and the photobiomodulation of the taste buds and salivary glands, it will present results of reducing the manifestation of dysgeusia as a sequel of the coronavirus (COVID-19). | — |
Countries
Brazil
Contacts
Pontifícia Universidade Católica de Campinas