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Tinnitus suppression with electrical stimulation using cochlear implants.

Tinnitus suppression with electrical stimulation using cochlear implants.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON20130
Enrollment
10
Registered
2012-04-05
Start date
2012-06-01
Completion date
Unknown
Last updated
2025-09-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tinnitus is a symptom defined as a perceived sound in the absence of an external source. Its prevalence is reported to be about 10%-15% of the general population and currently there is no cure for tinnitus. Recent research showed that changes in neuronal activity might underlie tinnitus pathology. Several recent studies, which are in general case-reports, show that tinnitus complaints may be reduced by restoring peripheral auditory neural activity by means of intracochlear electrical stimulation

Interventions

This study consists of two parts in which every part investigates a single research question. First the effect of electrical stimulation level (current level) on trinnitus intensity will be investigat

Sponsors

Maastricht University Medical Center (MUMC+)
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. CI-patients (implanted > ¾ year ago); 2. Experiencing tinnitus which is: A. Subjective (idiopathic); B. Localized ipsilateral to the CI; C. At least mild, that is: i. Visual Analogue Scale-score > 3; ii. Tinnitus Handicap Inventory-score > 16. D. Stable tinnitus (stable > 1/2 year). 3. Willingness to participate in this research (informed consent).

Exclusion criteria

Exclusion criteria: 1. Objective tinnitus; 2. Ménière’s disease; 3. Active middle ear disease; 4. Age < 18 years old.

Design outcomes

Primary

MeasureTime frame
The primary study variable is the intensity of the experienced tinnitus. Because tinnitus is a subjective phenomenon, its intensity is identified by means of VAS.

Secondary

MeasureTime frame
A secondary study endpoint of the present study is the experienced stimulus intensity, its intensity is identified by means of visual analogue scales (VAS).

Contacts

Public ContactR.A.G.J. Arts

KNO-afdeling Maastricht UMC+ Postbus 5800

remo.arts@mumc.nl+31 (0)43 3881184

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)