Investigating the effect of RTMS on tinnitus patients
Not Applicable
- Conditions
- tinnitus.TinnitusH93.1
- Registration Number
- IRCT20240319061335N1
- Lead Sponsor
- By the patient and resident (There is no cost at all)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- All
- Target Recruitment
- 30
Inclusion Criteria
A woman or man with tinnitus with an average age of 30 to 65 years2) ) No simultaneous use of drug treatments3) 4) 5)
Using the Tinnitus Handicap Inventory questionnaire2
Not using other treatment methods, including surgery and medicine, in the last 6 months
Absence of other effective diseases
Sound perception without any external physical stimulus
Exclusion Criteria
Having a middle ear infection
Having a job and activity with noise pollution
Tooth and sinus infection
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Tinnitus. Timepoint: tinnitus before the start of the intervention (first day); It is measured 20 days after the start of treatment and 50 days after the start of treatment in the follow-up phase. Method of measurement: Tinnitus Handicap Inventory.
- Secondary Outcome Measures
Name Time Method