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Electrical Vestibular Nerve Stimulation (VeNS): A Follow-up Assessment of Long-term Usage

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Neurovalens

Status

Completed

Conditions

Safety Issues

Treatments

Device: Vestal DM

Study type

Observational

Funder types

Industry
Other

Identifiers

NCT04783883
RWDMES01

Details and patient eligibility

About

A follow-up assessment study of the long-term safety of vestibular electrical stimulation as delivered by the Vestal DM Device.

Full description

A retrospective, open-label, follow-up study assessing the long-term safety and efficacy of vestibular electrical stimulation as delivered by the Vestal DM Device.

Enrollment

25 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Vestal DM user (more than 6 months)

Exclusion criteria

  • Vestal DM device user (less than 6 months)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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