Portable Neuromodulation Stimulator Registry for People With Multiple Sclerosis
Running, not enrolling
Conditions studied: Multiple Sclerosis
In brief
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 facts
- Study ID
- NCT06930339
- Run by
- Helius Medical Inc
- People needed
- 150
- Starts
- 2023-05-01
- Expected to finish
- 2026-04-30
- Last updated by the study team
- 2025-04-16
Who can join
Age: 22 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- Helius Medical — Newtown, Pennsylvania, United States
Full record on ClinicalTrials.gov
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