Phase
Condition
Tinnitus
Treatment
transcranial Random Noise Stimulation (tRNS) without acoustic stimulation (AS)
transcranial Random Noise Stimulation (tRNS) with acoustic stimulation (AS)
Clinical Study ID
Ages 18-75 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Male and female patients 18 years to 75 years of age (younger age limit according tocorona virus protection concepts and measures of the FOPH: Schutzkonzepte und -massnahmen (admin.ch))
Persistent chronic tinnitus with duration of more than 3 months
Signed Informed Consent after being informed about the study
Fluent in German or English
Tinnitus with a THI Grade 2 to 4 (18-76 points)
Willing and able to attend the study visits
Exclusion
Exclusion Criteria:
Actual neurological or psychiatric disorders
Hyperacusis
Regular intake of medication influencing the central nervous system (e.g.neuroleptics, hypnotics, sedatives, and anti-epileptics)
Implanted pacemaker
Surgical implants in the head region, such as cochlea implants
Asymmetrical hearing (more than 20dB side difference), pantonal hearing loss > 40dBin any measured frequency up to 2kHz
Women who are pregnant or breast feeding
Intention to become pregnant during the course of the study
Known or suspected non-compliance, drug or alcohol abuse
Participation in another study with investigational drug within the 30 dayspreceding and during the present study,
Enrolment of the investigator, his/her family members, employees and other dependentpersons
Study Design
Connect with a study center
University Hospital Zurich, University Zurich
Zurich, 8091
SwitzerlandActive - Recruiting
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