Tinnitus Patient Preferences Survey

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNicolas Gninenko

About this trial

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.

Eligibility criteria

Qualifiers

Individuals aged 18 or older suffering from subjective tinnitus

Self-reported or healthcare professional-diagnosed chronic (lasting 3 months or longer), subjective, burdensome tinnitus

Disqualifiers

Individuals under 18 years of age

Healthy volunteers without tinnitus

Trial design

Treatments tested in this trial

  • Survey using a questionnaire.

Treatment groups

500 Participants
are divided into 1 treatment group

Sponsors and collaborators

Nicolas Gninenko

Lead sponsor

Neurosoft Bioelectronics SA

Sponsor institution