Tinnitus, Subjective Clinical Trial
Official title:
Repetitive Transcranial Magnetic Stimulation for Chronic Subjective Non-Pulsatile Primary Tinnitus Compared to Placebo and Medicament Therapy
Verified date | June 2018 |
Source | University Hospital Ostrava |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Therapy of subjective chronic primary tinnitus could be challenging. Repetitive transcranial magnetic stimulation (rTMS) is currently being tested for suppressing the symptoms. However, effect of stimulation remains controversial. The aim was to uncover real effect of rTMS stimulation for tinnitus treatment. There will be three groups, stimulation group, sham stimulation group and controlled group with medicament treatment. The investigators assume that combination of rTMS stimulation of dorsolateral prefrontal cortex and primary auditory cortex at both sides will be more efficient. The investigators considered a 10% improvement in the tinnitus questionnaire score and in the tinnitus masking to be clinically relevant.
Status | Completed |
Enrollment | 40 |
Est. completion date | March 31, 2018 |
Est. primary completion date | March 31, 2018 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years to 99 Years |
Eligibility |
Inclusion Criteria: - subjective chronic non-pulsatile tinnitus lasting more than 6 months Exclusion Criteria: - head injury or brain surgery - epilepsy - organic brain lesion - Meniere's disease or fluctuating hearing loss - cochlear or bone-anchored hearing device implantation - history of suicide - pregnancy - therapy with anticonvulsants - antipsychotic medication - heart pacemaker implantation - rTMS performed in the past - not signing of the informed consent |
Country | Name | City | State |
---|---|---|---|
Czechia | University Hospital Ostrava | Ostrava | Moravian-Silesian Region |
Lead Sponsor | Collaborator |
---|---|
University Hospital Ostrava |
Czechia,
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* Note: There are 19 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Tinnitus Reaction Questionnaire (TRQ) | This questionnaire will be used to find out what sort of effects tinnitus has had on the lifestyle and general well-being of the patients. 10% improvement will be considered clinically relevant. | 36 months | |
Primary | Tinnitus Handicap Questionnaire (THQ) | This questionnaire has 27 questions and will be used to assess the degree of handicap that the tinnitus presents for the affected patients. 10% improvement will be considered clinically relevant. | 36 months | |
Primary | Tinnitus Handicap Inventory (THI) | The purpose of this questionnaire is to identify difficulties the affected patients may be experiencing because of tinnitus. 10% improvement of the score will be considered clinically relevant. | 36 months | |
Secondary | Improvement of depression - Beck Depression Inventory | Improvement of depressive symptoms in patients will be assessed using the Beck Depression Inventory (BDI) test. | 36 months | |
Secondary | Improvement of hearing loss - Fowler scoring | Improvement of the hearing loss in patients will be assessed using the pure-tone audiometry with Fowler scoring of hearing loss (%). | 36 months |
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