Clinical trial
Safety and Efficacy of the BrainPort™ Balance Device to Improve Balance in…
NCT00254228 · Wicab, Industry · Terminated
Key facts
| NCT number | NCT00254228 |
|---|---|
| Title | Safety and Efficacy of the BrainPort™ Balance Device to Improve Balance in Bilateral Vestibular Hypofunction |
| Official title | A Clinical Study to Evaluate the Safety and Efficacy of the BrainPort™ Balance Device When Used to Improve Postural Control in Subjects With Bilateral Vestibular Disorders |
| Lead sponsor | Wicab, Industry |
| Status | Terminated |
| Study type | Interventional |
| Conditions | Vestibular Disease |
| Intervention type | Device |
| Interventions | Electrotactile sensory substitution |
| Enrollment | 60 |
| Start date | Nov 1, 2005 |
| Completion | Dec 1, 2007 |
| First posted | Nov 15, 2005 |
| Last update posted | Oct 9, 2008 |
| Countries | United Kingdom, United States |
At a glance
- 1–9 Study sites
- No Results posted
- 1–9 Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: