Early Feasibility Study of the MyoRegulator® for Treatment of ALS

NACompletedINTERVENTIONAL
Enrollment

5

Participants

Timeline

Start Date

June 21, 2023

Primary Completion Date

July 31, 2024

Study Completion Date

August 31, 2024

Conditions
Amyotrophic Lateral Sclerosis
Interventions
DEVICE

MyoRegulator®

Study participants will receive treatment using the MyoRegulator® device 3 times a week for 2 x 30 minutes per session. The first week of treatment will be followed by a 1-week rest period with no treatments. Treatment sessions will then resume for 4 consecutive weeks, 3 times per week. A follow-up visit will be scheduled 4 weeks after the last treatment session.

Trial Locations (1)

02129

Spaulding Rehabilitation Hospital, Charlestown

Sponsors
All Listed Sponsors
collaborator

Spaulding Rehabilitation Hospital

OTHER

collaborator

Sean M. Healey & AMG Center for ALS

OTHER

collaborator

Muscular Dystrophy Association

OTHER

lead

PathMaker Neurosystems Inc.

INDUSTRY