Tinnitus Clinical Trial
Verified date | July 2018 |
Source | University of California, Irvine |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine the efficacy of a customized sound therapy in reducing tinnitus loudness and increasing the residual inhibition.
Status | Completed |
Enrollment | 31 |
Est. completion date | January 2015 |
Est. primary completion date | January 2015 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - 18 years or older - Male or female - Tinnitus present for 6 months or more - Adequate command of English Exclusion Criteria: - Active illicit drug use, alcohol dependence - Treatable cause of tinnitus - History of psychosis - Subjects on medications known to cause tinnitus (aspirin, ibuprofen, naproxen) which could not be stopped will be excluded. |
Country | Name | City | State |
---|---|---|---|
United States | UC Irvine Medical Center | Orange | California |
Lead Sponsor | Collaborator |
---|---|
University of California, Irvine |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in score of tinnitus loudness | 0, 1 minute; 1 hour; 1, 2, 4 and 6 months | ||
Primary | Change in score of tinnitus annoyance | 0, 1 minute; 1 hour; 1, 2, 4 and 6 months | ||
Primary | Change in residual inhibition | 1 minute; 1 hour; 1, 2, 4 and 6 months | ||
Primary | Change in score of Tinnitus Handicap Inventory (THI) | 0, 1, 2, 4 and 6 months |
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