Clinical study of the application of Light Therapy in the treatment of Taste Disorders in post-COVID-19 patients
- Conditions
- DysgeusiaCOVID-19Taste disorders.
- Registration Number
- RBR-2mfbkkk
- Lead Sponsor
- Pontifícia Universidade Católica de Campinas
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot yet recruiting
- Sex
- Not specified
- Target Recruitment
- Not specified
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
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
Study & Design
- Study Type
- Intervention
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 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).
- Secondary Outcome Measures
Name Time Method 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.