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ACTIVE NOT RECRUITING
NCT06930339

Portable Neuromodulation Stimulator Registry for People With Multiple Sclerosis

Sponsor: Helius Medical Inc

View on ClinicalTrials.gov

Summary

The Registry will be designed to gather information over 3 years. This important health economic information will help to establish the value of the PoNS Device on key therapeutic outcomes. These outcomes will include: disease-associated injury risks (i.e., falls), onset of new comorbidities and/or worsening/improvement of existing medical condition(s) (other than gait deficit/impairment), need for new pharmacological/non-pharmacological intervention or increase/decrease of ongoing pharmacotherapy or other non-pharmacological intervention, increase/decrease of in patient/outpatient hospital and/or office visits or stays, side effects. By participation in the Registry, patients and physicians will be providing Helius with access to information about medical history, medical diagnoses, clinical symptom presentations, vocational information, medications, pharmacologic and non-pharmacologic prescriptions, hospitalization and healthcare visits, and any reported therapy's adverse events.

Key Details

Gender

All

Age Range

22 Years - Any

Study Type

OBSERVATIONAL

Enrollment

150

Start Date

2023-05-01

Completion Date

2026-04-30

Last Updated

2025-04-16

Healthy Volunteers

No

Interventions

DEVICE

Portable Neuromodulation Stimulator (PoNS)

No intervention

Locations (1)

Helius Medical

Newtown, Pennsylvania, United States