Actively Recruiting
Tinnitus Patient Preferences Survey
Led by Nicolas Gninenko · Updated on 2026-04-08
500
Participants Needed
1
Research Sites
102 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
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.
CONDITIONS
Official Title
Tinnitus Patient Preferences Survey
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 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 will not qualify if you...
- Individuals under 18 years of age
- Healthy volunteers without tinnitus
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Neurosoft Bielectronics US Inc.
New York, New York, United States, 10016
Actively Recruiting
Research Team
N
Nicolas Gninenko, PhD
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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