ReWalk Personal Device Postmarket Study
NCT02944669 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 60
Last updated 2017-02-02
Summary
This study seeks to further evaluate the Multi-Tiered Training Program and to further explore the overall safety profile of the ReWalk Personal Device outside of the institutional setting under conditions of routine medical practice.
Conditions
- Injuries, Spinal Cord
Interventions
- DEVICE
-
ReWalk Personal Device
Sponsors & Collaborators
-
ReWalk Robotics, Inc.
lead INDUSTRY
Principal Investigators
-
Mathew Smuck, MD · Stanford University
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-06-30
- Primary Completion
- 2019-09-30
- Completion
- 2019-09-30
- FDA Device
- Yes
Countries
- United States
Study Locations
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