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Phoenix Exoskeleton for SCI Users

NCT03175055 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2018-06-01

No results posted yet for this study

Summary

This study will evaluate the Phoenix device for safety and effectiveness at allowing persons with SCI who are non-ambulatory or poorly ambulatory to stand up and walk under a variety of conditions.

Conditions

  • SCI - Spinal Cord Injury

Interventions

DEVICE

Phoenix

The study to assess safety and efficacy of Phoenix medical exoskeleton.

Sponsors & Collaborators

  • US Bionics

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-06-01
Primary Completion
2018-05-31
Completion
2018-05-31
FDA Device
Yes

Countries

  • United States
  • Hong Kong

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03175055 on ClinicalTrials.gov