Phase II Study of the Multichannel Auditory Brain Stem Implant for Deafness Following Surgery for Neurofibromatosis 2
NCT ID: NCT00004437
Last Updated: 2015-03-25
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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COMPLETED
PHASE2
INTERVENTIONAL
1999-10-31
2000-10-31
Brief Summary
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II. Optimize device fitting by combining monopolar and bipolar stimulation, and individual psychoacoustic channels for each patient, to increase the number of usable information channels for each patient and reduce or eliminate undesirable side effects.
III. Evaluate performance and learning effects using optimized fitting procedures.
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Detailed Description
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Patients are followed every 3 months for the first year, then annually thereafter.
Conditions
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Study Design
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TREATMENT
Interventions
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Multichannel Auditory Brain Stem Implant
Eligibility Criteria
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Inclusion Criteria
--Disease Characteristics-- Confirmed diagnosis of neurofibromatosis type 2 Scheduled to undergo first side or second side tumor removal First side implantation performed only on patients with onset of symptoms prior to age 40 --Prior/Concurrent Therapy-- If a nonfunctional auditory brain stem implant (ABI) is present (implanted during the removal of a first side tumor), a multichannel ABI may be implanted during the removal of a second side tumor --Patient Characteristics-- English is the primary language
12 Years
ALL
No
Sponsors
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Cochlear
INDUSTRY
FDA Office of Orphan Products Development
FED
Principal Investigators
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Steven J. Staller
Role: STUDY_CHAIR
Cochlear
Other Identifiers
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CC-FDR001283
Identifier Type: -
Identifier Source: secondary_id
199/13400
Identifier Type: -
Identifier Source: org_study_id
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