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Customized Acoustic Stimulation for the Treatment of Tinnitus

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01487447
Enrollment
31
Registered
2011-12-07
Start date
2010-01-31
Completion date
2015-01-31
Last updated
2020-01-30

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Tinnitus

Brief summary

The purpose of this study is to determine the efficacy of a customized sound therapy in reducing tinnitus loudness and increasing the residual inhibition.

Interventions

OTHERCustomized sound

treatment with customized sound therapy

OTHERRegular Masker

treatment with white noise

Sponsors

University of California, Irvine
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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.

Design outcomes

Primary

MeasureTime frame
Change in score of tinnitus loudness0, 1 minute; 1 hour; 1, 2, 4 and 6 months
Change in score of tinnitus annoyance0, 1 minute; 1 hour; 1, 2, 4 and 6 months
Change in residual inhibition1 minute; 1 hour; 1, 2, 4 and 6 months
Change in score of Tinnitus Handicap Inventory (THI)0, 1, 2, 4 and 6 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026