# Safety and Efficacy of the BrainPort™ Balance Device to Improve Balance in Bilateral Vestibular Hypofunction

> **NCT00254228** · NA · TERMINATED · sponsor: **Wicab** · enrollment: 60 (—)

## Conditions studied

- Vestibular Disease

## Interventions

- **DEVICE:** Electrotactile sensory substitution

## Key facts

- **NCT ID:** NCT00254228
- **Lead sponsor:** Wicab
- **Sponsor class:** INDUSTRY
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** TERMINATED
- **Start date:** 2005-11
- **Primary completion:** —
- **Final completion:** 2007-12
- **Target enrollment:** 60 (—)
- **Why stopped:** Terminated due to slow recruitment
- **Last updated:** 2008-10-09


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00254228

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00254228, "Safety and Efficacy of the BrainPort™ Balance Device to Improve Balance in Bilateral Vestibular Hypofunction". Retrieved via AI Analytics 2026-06-10 from https://api.ai-analytics.org/clinical/NCT00254228. Licensed CC0.

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