tinnitus
Conditions
Interventions
The clinical procedure will be carried out in an office associated with the Biophotonics Laboratory of the USP Physics Institute of São Carlos (IFSC). Forty female and male volunteers, aged between 18
E07.632.490
D03.383.606.450
Sponsors
Universidade de São Paulo
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior
Eligibility
Age
18 Years to 60 Years
Inclusion criteria
Inclusion criteria: Will be selected 40 volunteers (female or male), aged between 18 and 60 years with tinnitus complaint.
Exclusion criteria
Exclusion criteria: Patients under 18 years old and over 60 years old will be excluded. Patients with diabetes and uncontrolled cardiovascular problems will also be excluded
Design outcomes
Secondary
| Measure | Time frame |
|---|---|
| Secondary outcomes are not expected | — |
Primary
| Measure | Time frame |
|---|---|
| The evaluations will be carried out in the pre (T=0) and post-treatment (t=1) periods, as well as after 1 month of the last application (t=2). The execution time of the practical part of the project will last approximately 3 months. After the end of the research, patients in Group A (control), who will only carry out the pre- and post-treatment evaluations, will be invited to undergo treatment with vacuum therapy and laser. The expectation is that the elimination of tinnitus will occur. This result would prove the efficacy of tinnitus treatment using laser combined with vacuum therapy | — |
Countries
Brazil
Contacts
Public ContactVitor Panhóca
Laboratório de Biofotônica - Grupo de Ótica - Universidade de São Paulo
Outcome results
None listed