NCT06374264

Acceptability and Safety of MR-C-014 in Persons With Neuromyelitis Optica Spectrum Disorder

Enrolling by Invitation
NAAges 18–70InterventionalTreatment
MedRhythms, Inc.
~30 participants
Updated 2026-07-06 on ClinicalTrials.gov
What's tested:MR-C-014

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Participant acceptability of MR-C-014
Measured over Intervention period (of up to 8 weeks)
+1 more outcome measured
Neuromyelitis Optica Spectrum Disorder
2 sites across 2 states
Georgia1
Massachusetts1
  • Eric Klawiter, MD · PRINCIPAL_INVESTIGATOR · Massachusetts General Hospital

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Participant acceptability of MR-C-014Intervention period (of up to 8 weeks)

    Assesses participant engagement via logged use of MR-C-014

  • Number of device-related adverse events (AEs)Weekly for up to 8 weeks

    Assesses the safety of MR-C-014 in NMOSD patients with a gait deficit