Tinnitus
Conditions
Interventions
It's an open-label, two-arm, non-randomized controlled clinical study. Experimental group: 11 patients received three weekly sessions of dry needling in muscles with myofascial trigger points among th
Sponsors
Hospital Edmundo Vasconcelos / Fundação Instituto de Moléstias do Aparelho Digestivo e da Nutrição
Hospital Edmundo Vasconcelos / Fundação Instituto de Moléstias do Aparelho Digestivo e da Nutrição
Eligibility
Age
18 Years to No maximum
Inclusion criteria
Inclusion criteria: Patients over 18 years old; tinnitus for at least 3 months; trigger points on physical examination
Exclusion criteria
Exclusion criteria: Pulsatile tinnitus; coagulopathy or anticoagulant use; dermatological lesion at the needling site; pregnancy; needle phobia
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The expected outcome is a reduction in tinnitus intensity, assessed using the Tinnitus Handicap Inventory (THI) and the Visual Analog Scale (VAS) | — |
Secondary
| Measure | Time frame |
|---|---|
| No secondary outcomes are expected | — |
Countries
Brazil
Contacts
Public ContactArthur Nunes
Hospital Edmundo Vasconcelos / Fundação Instituto de Moléstias do Aparelho Digestivo e da Nutrição
Outcome results
None listed