Task-Based Functional MRI (fMRI) in Patients With Severely Bothersome Tinnitus
NCT ID: NCT01172262
Last Updated: 2018-05-03
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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WITHDRAWN
OBSERVATIONAL
2011-02-28
2012-02-29
Brief Summary
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Detailed Description
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This will be an experimental task-based fMRI pilot study involving the neurocognitive and neuroimaging assessment of patients with severely bothersome tinnitus.
The investigators plan to perform a pilot study and enroll a total of 10 subjects to undergo task-based imaging. These results will be compared to a control (no tinnitus) cohort (n=35) that has already undergone task-based fMRI. This task-based paradigm will allow us to advance knowledge about the role of the attention, control, and other cortical networks in the development and maintenance of bothersome tinnitus.
The investigators anticipate it will take one year to successfully enroll and test a total of 10 patients. All scans will be performed on the Washington University grounds.
Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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Bothered Tinnitus
Either responds with a Global Tinnitus Scale of Moderately or Severely Bothered. Score \>30 on the Tinnitus Handicap Index (THI).
MRI
This is an observational study, no intervention will occur.
Interventions
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MRI
This is an observational study, no intervention will occur.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
* Subjective, unilateral or bilateral, non-pulsatile tinnitus of 6 month's duration or greater
* Either "moderately bothered" or "severely bothered" on the Global Bothersome scale
* Able to give informed consent
* Able to read, write, speak and understand English fluently
* If applicable, a negative urine pregnancy test
* An audiogram within the past 12 months
* THI score \>38
Exclusion Criteria
* Patients with hyperacusis or misophonia (hyper-sensitivity to noises)
* Patients with cardiac pacemakers, intracardiac lines, implanted medication pumps, implanted electrodes in the brain, or any other contraindication for MRI scan
* Patients with an acute or chronic unstable medical condition which, in the opinion of the investigator, would require stabilization prior to initiation of magnetic stimulation
* Patients with any active ear disease that, in the opinion of the PI, needs to be further evaluated
* Patients with symptoms of depression as evidenced by a score of 14 or greater on the Beck Depression Inventory
* Any psychiatric co-morbidity that may complicate the interpretation of study results
* Any tinnitus related to a Workman's Compensation claim or litigation-related event
* Weight over 300 pounds
* A Mini-Mental Status Exam score less than 27
* Patients with a history of claustrophobia
* Inability to lay flat for 2 hour
* Active alcohol and/or drug dependence or history of alcohol and/or drug dependence within the last year
* Any medical condition that, in the opinion of the investigators, confounds study results or places the subject at greater risk
* Unable to provide informed consent
* Currently pregnant
18 Years
60 Years
ALL
No
Sponsors
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Washington University School of Medicine
OTHER
Responsible Party
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Principal Investigators
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Andre M Wineland, MD
Role: PRINCIPAL_INVESTIGATOR
Washington University School of Medicine
Other Identifiers
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Bothersome Tinnitus
Identifier Type: OTHER
Identifier Source: secondary_id
AMW04292010
Identifier Type: -
Identifier Source: org_study_id
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