Safety and Efficacy of the BrainPort™ Balance Device to Improve Balance in Bilateral Vestibular Hypofunction
NCT00254228 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 60
Last updated 2008-10-09
Summary
The purpose of this study is to determine whether the BrainPort™ balance device is safe and effective in the treatment of balance disorders in patients with Bilateral Vestibular Dysfunction.
Conditions
- Vestibular Disease
Interventions
- DEVICE
-
Electrotactile sensory substitution
Sponsors & Collaborators
-
Wicab
lead INDUSTRY
Principal Investigators
-
Yuri P Danilov, PhD · Wicab
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- DOUBLE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Max Age
- 85 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2005-11-30
- Completion
- 2007-12-31
Countries
- United States
- United Kingdom
Study Locations
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