Resting-State Neural Connectivity in Patients With Subjective Tinnitus Without Bother

Tinnitus Clinical Trial

Official title:

Resting-State Neural Connectivity in Patients With Subjective Tinnitus Without Bother

Clinical Trial Details — Status: Unknown status

Administrative data

• NCT number: NCT01049828
• Other study ID #: WU01201982
• Status: Unknown status
• Phase: N/A
• First received: January 14, 2010
• Last updated: July 29, 2011
• Start date: August 2010
• Est. completion date: May 2012

Study information

• Verified date: July 2011
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Tinnitus is the occurrence of an auditory sensation without the presence of an acoustic stimulus. Approximately, 50 million people in the United States experience chronic tinnitus and 15 million of these people have bothersome tinnitus. Several studies have shown that people who are bothered by their tinnitus have difficulty in concentration and focus. Through imaging modalities we have deranged neural networks responsible for attention. Only 20 percent of patients diagnosed with tinnitus are severely bothered. We seek the following:

1. Match a group of non-bothered tinnitus patients on age and hearing status to an existing cohort of bothered tinnitus patients.

2. Assess the resting-state neural connectivity in patients with non-bothersome tinnitus. Findings from the comparison of functional connectivity magnetic resonance imaging (fcMRI) from subjects with bothersome tinnitus in our current rTMS clinical trial to normal age-matched controls without tinnitus demonstrates that subjects with bothersome tinnitus have dramatic alterations in cortical attention and control networks. Our hypothesis is that the fcMRI-defined changes in the attention and control networks reflect the impact of excessive auditory stimulation in patients with bothersome tinnitus and explains the difficulty with concentration, short-term memory, and other common problems. To fully test this hypothesis we need to obtain fcMRI of the attention network among subjects with tinnitus but without bother and compare the status of their neural networks with those of tinnitus subjects with bother and with normal controls.

3. Compare the resting cortical networks in subjects with non-bothersome tinnitus to subjects with bothersome tinnitus and subjects without tinnitus Our null hypothesis is that there are no differences in the resting-state cortical networks, especially the attention and control networks, between tinnitus patients who do not experience bother, tinnitus patients who do experience bother, and subjects without tinnitus. Through fcMRI, we will examine correlations in blood oxygen level dependent (BOLD) signals in established auditory, attention, control, and other brain regions in the resting brain and compare these findings to already collected fcMRI scans of bothered tinnitus patients, and controls (patients without tinnitus).

Recruitment information / eligibility

• Status: Unknown status
• Enrollment: 19
• Est. completion date: May 2012
• Est. primary completion date: May 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 45 Years to 60 Years

Eligibility

Inclusion Criteria:

• Men and women between the ages of 45 and 60 years

• Subjective, unilateral or bilateral, non-pulsatile tinnitus of 6 month's duration or greater

• A recent audiogram (within 6 months)

• Either "not bothered" or "bothered a little" on the Global Bothersome scale

• Able to give informed consent

• English-speaking

Exclusion Criteria:

• Patients experiencing tinnitus related to cochlear implantation, retrocochlear lesion, or other known anatomic/structural lesions of the ear and temporal bone

• Patients with hyperacusis or misophonia (hyper-sensitivity to loud noises)

• Patients with cardiac pacemakers, intracardiac lines, implanted medication pumps, implanted electrodes in the brain, other intracranial metal objects with the exception of dental fillings, 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 or, in the opinion of the psychiatric sub-investigator demonstrates active mood symptoms that meet DSM-IV-TR criteria for Major Depressive Disorder

• Any psychiatric co-morbidity that, in the opinion of the psychiatric sub-investigator, may complicate the interpretation of study results

• Patients with tinnitus related to Workman's Compensation claim or litigation-related event

• Weight over 350 pounds

• A Mini-Mental Status Exam score less than 27

• Patients with a history of claustrophobia

• Inability to lay flat for 2 hours

• 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

• Any exclusions from radiology screening Currently Pregnant

Related Conditions & MeSH terms

• Tinnitus

Intervention

Other:
• No intervention
No treatment for tinnitus will occur in this study.

Locations

Country	Name	City	State
United States	Washington University, Center for Clinical Studies	St. Louis	Missouri

Sponsors (1)

Lead Sponsor	Collaborator
Washington University School of Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Recruit 20 participants and have them undergo both neuro-cognitive and neuro-imaging testing.		8 months