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Phoenix Exoskeleton for SCI Users

Primary Purpose

SCI - Spinal Cord Injury

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Phoenix
Sponsored by
US Bionics
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for SCI - Spinal Cord Injury

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. 18 Years of age or older in general good health
  2. Weigh no more than 220lbs
  3. Skin must be healthy where it touches the Phoenix
  4. Able to stand using a device such as a standing frame
  5. Have enough strength in your hands and shoulders to support yourself standing and walking using crutches or a walker
  6. Have good control of upper body
  7. Determined to have enough bone health to walk full weight bearing without risk of fracture. Meeting of this condition is at the discretion of your personal MD
  8. Passive range of motion (PROM) at shoulders, trunk, upper extremities and lower extremities within functional limits for safe gait and use of appropriate assistive device/stability aid
  9. Hip width no greater than 18" (46 cm) measured when sitting.
  10. Femur length between 12.3 inches (31.3 cm) and 19.8 inches (50.2 cm) measured between centers of hip and knee joints.
  11. Tibia length between 13.4 inches (33.9 cm) and 22 (55.9 cm) inches measured between the knee joint and bottom of the foot.
  12. In general good health and able to tolerate moderate levels of activity.
  13. Blood pressure and heart rate within established guidelines for locomotive training:

At rest; Systolic 150 or less Diastolic 90 or less and Heart rate 100 or less Exercise; Systolic 180 or less Diastolic 105 or less and Heart Rate 145 or less

Exclusion Criteria:

  • 1. Pregnant or lactating females 2. Spinal cord injury level higher than T4 3. Severe muscle stiffness/tightness 4. Significant spasticity (Modified Ashworth Scale score of 3 or above) 5. Trunk or lower extremity pressure ulcer 6. Open Wounds 7. Unstable spine, un-healed limbs, or fractures 8. Severe sensitivity to touch 9. Presence of bone in soft tissue where bone normally does not exist (heterotopic ossification), limiting range of motion in the hip or knee joints 10. Joint instability, dislocation, moderate to severe hip dysplasia 11. Significant scoliosis (>40 degrees) 12. Hardware, implant, or any external device impeding with safe fitting or use of Phoenix 13. Femoral or tibial rotation deformity (>15 degrees) 14. Significant flexion contractures limited to 35º at the hip and 20º at the knee 15. Uncontrolled seizures, musculoskeletal injury, fracture or lower-limb surgery in past year.

    16. Known history of pulmonary disease limiting exercise tolerance or history of cardiac disease 17. Psychopathology, or other condition that the physician or investigator, in his or her clinical judgment, considers to be exclusionary to safely use an exoskeleton.

    18. Severe concurrent medical diseases, illness, systemic or peripheral infection 19. Dizziness or headache with standing 20. History of autonomic dysreflexia 21. Orthostatic Hypotension: Decrease in Systolic BP > 20, Diastolic BP > 10 upon standing from a seated position.

Sites / Locations

  • suitX
  • Motion & Gait Lab, Lucile Packard Children's Hospital Stanford
  • St. David's Medical Center, Rehabilitation Hospital
  • The University of Hong Kong

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Phoenix

Arm Description

Phoenix

Outcomes

Primary Outcome Measures

Timed Up and Go (TUG)
6 Minute Walk Test (6MWT)
10 Meter Walk Test (10MWT)

Secondary Outcome Measures

Surface Walk Test
Testing the ability to ambulate with the device on a variety of surfaces

Full Information

First Posted
May 31, 2017
Last Updated
May 30, 2018
Sponsor
US Bionics
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1. Study Identification

Unique Protocol Identification Number
NCT03175055
Brief Title
Phoenix Exoskeleton for SCI Users
Official Title
Phoenix Exoskeleton Clinical Study
Study Type
Interventional

2. Study Status

Record Verification Date
May 2018
Overall Recruitment Status
Completed
Study Start Date
June 1, 2017 (Actual)
Primary Completion Date
May 31, 2018 (Actual)
Study Completion Date
May 31, 2018 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Bionics

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Device Product Not Approved or Cleared by U.S. FDA
Yes
Product Manufactured in and Exported from the U.S.
Yes

5. Study Description

Brief 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
SCI - Spinal Cord Injury

7. Study Design

Primary Purpose
Other
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Phoenix
Arm Type
Experimental
Arm Description
Phoenix
Intervention Type
Device
Intervention Name(s)
Phoenix
Intervention Description
The study to assess safety and efficacy of Phoenix medical exoskeleton.
Primary Outcome Measure Information:
Title
Timed Up and Go (TUG)
Time Frame
10 weeks
Title
6 Minute Walk Test (6MWT)
Time Frame
10 weeks
Title
10 Meter Walk Test (10MWT)
Time Frame
10 weeks
Secondary Outcome Measure Information:
Title
Surface Walk Test
Description
Testing the ability to ambulate with the device on a variety of surfaces
Time Frame
10 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 Years of age or older in general good health Weigh no more than 220lbs Skin must be healthy where it touches the Phoenix Able to stand using a device such as a standing frame Have enough strength in your hands and shoulders to support yourself standing and walking using crutches or a walker Have good control of upper body Determined to have enough bone health to walk full weight bearing without risk of fracture. Meeting of this condition is at the discretion of your personal MD Passive range of motion (PROM) at shoulders, trunk, upper extremities and lower extremities within functional limits for safe gait and use of appropriate assistive device/stability aid Hip width no greater than 18" (46 cm) measured when sitting. Femur length between 12.3 inches (31.3 cm) and 19.8 inches (50.2 cm) measured between centers of hip and knee joints. Tibia length between 13.4 inches (33.9 cm) and 22 (55.9 cm) inches measured between the knee joint and bottom of the foot. In general good health and able to tolerate moderate levels of activity. Blood pressure and heart rate within established guidelines for locomotive training: At rest; Systolic 150 or less Diastolic 90 or less and Heart rate 100 or less Exercise; Systolic 180 or less Diastolic 105 or less and Heart Rate 145 or less Exclusion Criteria: 1. Pregnant or lactating females 2. Spinal cord injury level higher than T4 3. Severe muscle stiffness/tightness 4. Significant spasticity (Modified Ashworth Scale score of 3 or above) 5. Trunk or lower extremity pressure ulcer 6. Open Wounds 7. Unstable spine, un-healed limbs, or fractures 8. Severe sensitivity to touch 9. Presence of bone in soft tissue where bone normally does not exist (heterotopic ossification), limiting range of motion in the hip or knee joints 10. Joint instability, dislocation, moderate to severe hip dysplasia 11. Significant scoliosis (>40 degrees) 12. Hardware, implant, or any external device impeding with safe fitting or use of Phoenix 13. Femoral or tibial rotation deformity (>15 degrees) 14. Significant flexion contractures limited to 35º at the hip and 20º at the knee 15. Uncontrolled seizures, musculoskeletal injury, fracture or lower-limb surgery in past year. 16. Known history of pulmonary disease limiting exercise tolerance or history of cardiac disease 17. Psychopathology, or other condition that the physician or investigator, in his or her clinical judgment, considers to be exclusionary to safely use an exoskeleton. 18. Severe concurrent medical diseases, illness, systemic or peripheral infection 19. Dizziness or headache with standing 20. History of autonomic dysreflexia 21. Orthostatic Hypotension: Decrease in Systolic BP > 20, Diastolic BP > 10 upon standing from a seated position.
Facility Information:
Facility Name
suitX
City
Emeryville
State/Province
California
ZIP/Postal Code
94608
Country
United States
Facility Name
Motion & Gait Lab, Lucile Packard Children's Hospital Stanford
City
Menlo Park
State/Province
California
ZIP/Postal Code
94025
Country
United States
Facility Name
St. David's Medical Center, Rehabilitation Hospital
City
Austin
State/Province
Texas
ZIP/Postal Code
78705
Country
United States
Facility Name
The University of Hong Kong
City
Hong Kong
Country
Hong Kong

12. IPD Sharing Statement

Plan to Share IPD
Undecided

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Phoenix Exoskeleton for SCI Users

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