Tinnitus Patient Preferences Survey

Recruiting now

Conditions studied: Tinnitus, Subjective, Tinnitus, Bilateral, Tinnitus, Noise Induced, Tinnitus, Hearing Loss, Cochlear Implant Users

In brief

The goal of this survey is to assess several aspects related to patient preferences regarding interventions for alleviating tinnitus through invasive electrical brain stimulation (neuromodulation). This survey covers the acceptance of a surgically-placed brain implant, of its associated risks related to the neurosurgical procedure, usability considerations, and the willingness/ability to pay for such a treatment. Neurosoft Bioelectronics will use the collected patients' feedback and usability preferences data for the development of a novel minimally invasive brain implant aimed at alleviating tinnitus.

Key facts

Study ID

NCT06782308

Run by

Nicolas Gninenko

People needed

500

Starts

2025-01-13

Expected to finish

2026-12-30

Last updated by the study team

2026-04-08

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Individuals aged 18 or older suffering from subjective tinnitus
• Self-reported or healthcare professional-diagnosed chronic (lasting 3 months or longer), subjective, burdensome tinnitus

You may not qualify if…

• Individuals under 18 years of age
• Healthy volunteers without tinnitus

Where it is running

• Neurosoft Bielectronics US Inc. — New York, New York, United States (enrolling)

Full record on ClinicalTrials.gov

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