Saves the questions and what to expect into your notes, next to the visit they belong to.
Keep this study
Lead
University of Minnesota
This study is not specifically seeking to treat tinnitus but is designed to investigate various mSync parameters that can alter the tinnitus percept. Findings from this study will help identify specific mSync parameters that can be more effective at decreasing or fully suppressing the tinnitus percept that will be systematically explored in a follow-up study.
Age
18–65
Sex
ALL
Healthy volunteers
Not accepted
You may be eligible if
Have subjective, non-pulsatile, and bothersome tinnitus
Will not start any new tinnitus treatment during the study
Ability to give informed consent and understand study objectives in English
Willing and able to understand and comply with all study-related procedures
You may not be if
Substantial hearing loss or hyperacusis that may interfere with the study
Medical history of other ear or brain disorders, history of seizures, or currently using any medication or treatments that can cause or increase the chances of seizures
Any implanted medical or metal device, such as a pacemaker, aneurysm clip, or cochlear implant
Pregnant or currently breast-feeding (we need to give all female subjects a pregnancy test because pregnant females and unborn children need extra protection for their safety)
Any handicap that prevents the subject from reliably performing the tests
