Chronic Electrical Stimulation of the Auditory Cortex for Intractable Tinnitus (ACOUSCO)
Primary Purpose
Hearing Disorders, Hearing Loss, Hyperacusis
Status
Completed
Phase
Phase 2
Locations
France
Study Type
Interventional
Intervention
significant chronic primary auditory cortex stimulation during the first two weeks
non significant chronic primary auditory cortex stimulation during the first two weeks
Sponsored by
About this trial
This is an interventional treatment trial for Hearing Disorders focused on measuring Hearing Disorders, Hearing Loss, Hyperacusis, Tinnitus, chronic cortical stimulation, functional magnetic resonance imaging
Eligibility Criteria
Inclusion Criteria:
- Patient > 18 years of age and < 70 years of age
- Permanent and chronic tinnitus during more than 2 years
- A score over 19 at the STI (Quality of life index)
Exclusion Criteria:
- Deaf person
- Surgical or anesthetic contraindication
- History of psychiatric disorder or suicide
- Epilepsia
Sites / Locations
- University Hospital of Bordeaux - Pellegrin
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Experimental
Arm Label
1
2
Arm Description
Outcomes
Primary Outcome Measures
intensity of the tinnitus. The cut off efficacy is 35% improvement on the STI score
Secondary Outcome Measures
Tinnitus Handicap Questionnaire Multiple Activity Scale for Hyperacusis questionnaires for assessment of the patients and treatment outcome of tinnitus hyperacusis and loss of hearing subjective global improvement scale
Full Information
NCT ID
NCT00486577
First Posted
June 13, 2007
Last Updated
January 27, 2011
Sponsor
University Hospital, Bordeaux
1. Study Identification
Unique Protocol Identification Number
NCT00486577
Brief Title
Chronic Electrical Stimulation of the Auditory Cortex for Intractable Tinnitus
Acronym
ACOUSCO
Official Title
Chronic Electrical Stimulation of the Auditory Cortex for Intractable Tinnitus
Study Type
Interventional
2. Study Status
Record Verification Date
January 2011
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
December 2010 (Actual)
Study Completion Date
December 2010 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
University Hospital, Bordeaux
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this study is to determine whether chronic electrical stimulation of the primary auditory cortex is effective in the treatment of chronic, severe and intractable tinnitus
Detailed Description
Severe and chronic tinnitus - the perception of sound in one or both ears or in the head when non-external sound is present - can be disabling and difficult to treat. Physiopathology of tinnitus can be considered as similar to neuropathic pain. Neuropathic and central pain are treated since ten years by chronic electrical motor cortex stimulation. The hypothesis of this study is that it will be possible to treat severe tinnitus by this stimulation as neuropathic pains are treated by motor cortical stimulation.
Principal Objective : to evaluate the efficacy of chronic electrical stimulation of the auditory cortex for intractable tinnitus
Secondary Objective : to evaluate the tolerability and the safety of chronic electrical stimulation of the auditory cortex for intractable tinnitus
Study design : randomized, cross over, double blind, study to evaluate the efficacy of the chronic electrical stimulation versus sham in severe and chronic tinnitus
Inclusion criteria :
Patient >18 years of age and < 70 years of age Permanent and chronic tinnitus during more than 2 years. A score over 19 at the STI (Quality of life index for tinnitus) Unilateral tinnitus
• Exclusion criteria : Deaf person Surgical or anesthetic contraindication History of psychiatric disorder or suicide Epilepsia
• Number of subjects : 10
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hearing Disorders, Hearing Loss, Hyperacusis, Tinnitus
Keywords
Hearing Disorders, Hearing Loss, Hyperacusis, Tinnitus, chronic cortical stimulation, functional magnetic resonance imaging
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 2, Phase 3
Interventional Study Model
Crossover Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
10 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Title
2
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
significant chronic primary auditory cortex stimulation during the first two weeks
Intervention Description
significant chronic primary auditory cortex stimulation during the first two weeks of the follow up than wash out period followed by two weeks of non significant stimulation
Intervention Type
Procedure
Intervention Name(s)
non significant chronic primary auditory cortex stimulation during the first two weeks
Intervention Description
non significant stimulation during the first two weeks of the follow up than wash out period followed by two weeks of significant chronic primary auditory cortex stimulation
Primary Outcome Measure Information:
Title
intensity of the tinnitus. The cut off efficacy is 35% improvement on the STI score
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Tinnitus Handicap Questionnaire Multiple Activity Scale for Hyperacusis questionnaires for assessment of the patients and treatment outcome of tinnitus hyperacusis and loss of hearing subjective global improvement scale
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patient > 18 years of age and < 70 years of age
Permanent and chronic tinnitus during more than 2 years
A score over 19 at the STI (Quality of life index)
Exclusion Criteria:
Deaf person
Surgical or anesthetic contraindication
History of psychiatric disorder or suicide
Epilepsia
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Emmanuel Cuny, MD
Organizational Affiliation
University Hospital, Bordeaux
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital of Bordeaux - Pellegrin
City
Bordeaux
ZIP/Postal Code
33 076
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
25017670
Citation
Engelhardt J, Dauman R, Arne P, Allard M, Dauman N, Branchard O, Perez P, Germain C, Caire F, Bonnard D, Cuny E. Effect of chronic cortical stimulation on chronic severe tinnitus: a prospective randomized double-blind cross-over trial and long-term follow up. Brain Stimul. 2014 Sep-Oct;7(5):694-700. doi: 10.1016/j.brs.2014.05.008. Epub 2014 Jun 4.
Results Reference
derived
Learn more about this trial
Chronic Electrical Stimulation of the Auditory Cortex for Intractable Tinnitus
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