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Sponsored by: |
Department of Veterans Affairs |
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Information provided by: | Department of Veterans Affairs |
ClinicalTrials.gov Identifier: | NCT00013390 |
The investigators propose to evaluate two different approaches to the alleviation of tinnitus symptoms by comparing changes from baseline performance on the Tinnitus Severity Index. They propose to provide an unbiased evaluation of competing methodologies. The design is one in which pairs of prospective subjects are randomly assigned to one of two treatment groups. Changes in group performance will be compared for selected measures.
Condition | Intervention | Phase |
---|---|---|
Tinnitus |
Procedure: Tinnitus |
Phase II |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Open Label, Active Control, Single Group Assignment, Efficacy Study |
Official Title: | Evaluation of Treatment Methods for Clinically Significant Tinnitus |
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Patients with significant tinnitus
United States, Oregon | |
VAMC, Portland | |
Portland, Oregon, United States |
Investigator: | John Fryer, Ph.D., Asst. Director | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
Investigator: | Nancy Rocheleau, Program Analyst | Department of Veterans Affairs, Program Analysis and Review Section (PARS), Rehabilitation Research & Development Service |
Study ID Numbers: | C1995R |
Study First Received: | March 14, 2001 |
Last Updated: | December 12, 2007 |
ClinicalTrials.gov Identifier: | NCT00013390 |
Health Authority: | United States: Federal Government |
Auditory, tinnitus |
Signs and Symptoms Sensation Disorders Hearing Disorders Otorhinolaryngologic Diseases |
Neurologic Manifestations Ear Diseases Tinnitus |
Nervous System Diseases |