Somatosensory Stimulation to Alleviate Tinnitus

Status Completed

Clinical Trial Summary

The purpose of this study is to develop and test a subject operated device to lessen tinnitus (ringing in the ear), based on subject-feedback for stimulus presentation.

Clinical Trial Description

This study enrolls 20 adult subjects. This project will develop and test a device with the ultimate goal of providing a patient operated device to alleviate phantom sound perception, or tinnitus, based on patient-feedback for stimulus presentation.

The device, an electrical-acoustical stimulus timing, is based on physiological findings of stimulus-timing-dependent plasticity in somatosensory and auditory nuclei,that when aberrant, contribute to tinnitus. ;

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Crossover Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Tinnitus

Clinical Trial Details

NCT number	NCT02974543
Study type	Interventional
Source	University of Michigan
Contact
Status	Completed
Phase	N/A
Start date	September 2014
Completion date	March 2016

View Details

See also
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