Deep Brain Stimulation for Refractory Tinnitus
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Tinnitus
- Sponsor
- Maastricht University Medical Center
- Enrollment
- 6
- Locations
- 1
- Primary Endpoint
- Change over time of the score on the Tinnitus Functional Index
- Status
- Completed
- Last Updated
- 9 months ago
Overview
Brief Summary
Tinnitus is the perception of a sound in the absence of an audible source. Currently up to 15% of the general population suffers chronically from tinnitus. The most severe degree of tinnitus ís experienced by 2.4% of the population and is associated with insomnia, depression; anxiety and even suicide. Up to date there is no effective standard therapy. Current therapies mostly focus on treating the distress caused by tinnitus instead of reducing the actual phantom sound. Nevertheless, many patients do not benefit from the current approaches and become severe and chronic tinnitus sufferers. In these patients neuromodulation-based treatments can be a promising option. Tinnitus perception is associated with many complex changes in several different brain structures. The general accepted hypothesis is that neuronal changes occur in both auditory and non-auditory brain structures, most often as a compensating mechanism on reduced input from the auditory nerve caused by cochlear hair cell damage. These central neuronal changes include an increase in spontaneous firing rate, synchronized activity, bursting activity and tonotopic reorganization. In high-frequency deep brain stimulation (DBS) a reversible lesion-like effect is mimicked. From findings in Parkinson's disease patients who also had tinnitus and were treated with DBS, it is known that stimulation can alter or even completely diminish perception of tinnitus. It can be expected that modulation of specific structures within the complex tinnitus pathways can disrupt pathological neuronal activity and thereby alter tinnitus perception or distress caused by this phantom sensation. The investigators found in animal studies that DBS in the central auditory pathway can indeed significantly decrease tinnitus-like behavior. In a questionnaire study the investigators found that around one-fifth of the patients would be reasonably willing to accept invasive treatments and one-fifth would be fully willing to undergo invasive treatment like DBS. Based on preclinical studies and human case studies, the investigators expect that DBS of the central auditory pathway will inhibit tinnitus perception and distress caused by this phantom sensation. Based on studies performed within Maastricht University Medical Center (MUMC), the investigators selected the medial geniculate body of the thalamus (MGB) as the most potential target to treat tinnitus with DBS.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Medically refractory tinnitus. Patient does not respond to available tinnitus treatments (hearing aids, cognitive treatments) and is thoroughly evaluated by the multidisciplinary tinnitus team in MUMC. Thus patients do not respond to both of the following treatments (i.e. TQ is still ≥ 47):
- •Hearing aids (except if hearing is normal)
- •Evidence-based cognitive treatment in Hoensbroek (Cima et al., 2012) or a similar version of this treatment in the MUMC
- •Minimum age 18 years, maximum age 69 years.
- •Experiencing tinnitus which is:
- •Not pulsatile
- •Unilateral or bilateral
- •Severe tinnitus (based on the TQ score ≥ 47)
- •Chronic and stable (present \> 2 years and stable \> 1 year).
- •Bilateral hearing of high tone Fletcher Index \< 60 dB
Exclusion Criteria
- •Anatomic cause of tinnitus (e.g. vestibular schwannoma, tumour, middle-ear pathology)
- •DSM-V psychiatric disorders, other than depression or anxiety disorder (such as bipolar disorder, dementia, addiction, personality disorders); diagnosed by a psychiatrist. A psychiatrist will screen the patients for this matter.
- •Depression or anxiety disorder which was already present before tinnitus. A psychiatrist will screen the patients for this matter.
- •Cognitive impairment (assessed with standard 'cognitive functioning battery test' questionnaires) or coping problems (CISS-21)
- •Active ear diseases that needs further attention according to research team
- •Pregnancy or breast-feeding
- •Active suicide thoughts or attempts
- •Underlying malignancies, whenever life expectancy is lower than 2 years
- •Other implantable electronic devices that potentially could interfere with DBS, e.g. cochlear implants, auditory brainstem implants or cortical implants
Outcomes
Primary Outcomes
Change over time of the score on the Tinnitus Functional Index
Time Frame: Week 1, week 20, week 26, week 33, week 60
A validated questionnaire which assesses the impact of tinnitus on a patient measured on multiple time points to measure a change over time. The TFI score can range from 0-100, higher values indicate more tinnitus burden. When a patient scores 54 or higher the tinnitus is considered to be a major problem.
Secondary Outcomes
- VAS Loudness(Week 1, week 12, week 20, week 26, week 33, week 60)
- VAS Burden(Week 1, week 12, week 20, week 26, week 33, week 60)
- 15 word memory test(Week 1, week 27, week 34, week 60)
- Phonemic Verbal Fluency Test (A)(Week 1, week 27, week 34, week 60)
- Phonemic Verbal Fluency Test (T)(Week 1, week 27, week 34, week 60)
- Beck Depression Inventory II (BDI-II)(Week 1, week 60)
- Stroop Color and Word Test(Week 1, week 27, week 34, week 60)
- Trail Making Test(Week 1, week 27, week 34, week 60)
- Phonemic Verbal Fluency Test (D)(Week 1, week 27, week 34, week 60)
- Quality of life Questionnaire(Week 1, week 27, week 34, week 60)
- Boston naming test(Week 1, week 27, week 34, week 60)
- Semantic Verbal Fluency Test (Animals)(Week 1, week 27, week 34, week 60)
- Semantic Verbal Fluency Test (Jobs)(Week 1, week 27, week 34, week 60)
- Beck Anxiety Inventory (BAI)(Week 1, week 60)
- Hospital Anxiety and Depression Scale (HADS)(Week 1, week 60)
- Audiometry(Week 1, week 14, week 27, week 34, week 60)
- Auditory Brainstem Response(Week 1, week 14, week 27, week 34, week 60)
- Electroencephalography (EEG)(Week 1, week 14, week 27, week 34, week 60)
- Local Field Potentials (LFP)(Week 12)