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Assessment of customized bimodal stimulation for tinnitus

Status: Recruiting

We are testing the usability of a medical device designed to treat tinnitus. The Lenire device is made by Neuromod Devices and is CE approved for use in Europe and FDA approved in the US. This neuromodulation device delivers sounds and tongue stimulation that work together to reduce tinnitus. We are interested in your feedback after using the Lenire device with the modified stimulation program. This research study lasts about 3 months.

I'm interested

Sex: Male or Female
Age Group: 18 years and over
This study is NOT accepting healthy volunteers
Inclusion Criteria:

• Subjective Tinnitus
• Tinnitus has a dominant pitch
• willing to commit to a12 week study
Exclusion Criteria:

• objective tinnitus
• started using hearing aids within the past 3 months
• have an electro-active implanted device
Conditions:

Ear, Nose & Throat

Keywords:

hearing, neuromodulation, Tinnitus, bimodal stimulation

Study Contact: Tinnitus Research Team STUDY - umntinnitus@umn.edu
Principal Investigator: Lei Feng
IRB Number: STUDY00024155

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